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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Molecular mechanisms underlying Th1-like Treg generation and function</title>
<author><name sortKey="Kitz, Alexandra" sort="Kitz, Alexandra" uniqKey="Kitz A" first="Alexandra" last="Kitz">Alexandra Kitz</name>
<affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Departments of Neurology and Immunobiology,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Dominguez Villar, Margarita" sort="Dominguez Villar, Margarita" uniqKey="Dominguez Villar M" first="Margarita" last="Dominguez-Villar">Margarita Dominguez-Villar</name>
<affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Department of Neurology, Human and Translational Immunology Program,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">28624966</idno>
<idno type="pmc">7079789</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079789</idno>
<idno type="RBID">PMC:7079789</idno>
<idno type="doi">10.1007/s00018-017-2569-y</idno>
<date when="2017">2017</date>
<idno type="wicri:Area/Pmc/Corpus">000373</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000373</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Molecular mechanisms underlying Th1-like Treg generation and function</title>
<author><name sortKey="Kitz, Alexandra" sort="Kitz, Alexandra" uniqKey="Kitz A" first="Alexandra" last="Kitz">Alexandra Kitz</name>
<affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Departments of Neurology and Immunobiology,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Dominguez Villar, Margarita" sort="Dominguez Villar, Margarita" uniqKey="Dominguez Villar M" first="Margarita" last="Dominguez-Villar">Margarita Dominguez-Villar</name>
<affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Department of Neurology, Human and Translational Immunology Program,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">Cellular and Molecular Life Sciences</title>
<idno type="ISSN">1420-682X</idno>
<idno type="eISSN">1420-9071</idno>
<imprint><date when="2017">2017</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p id="Par1">Since their ‘re-discovery’ more than two decades ago, FOXP3<sup>+</sup>
regulatory T cells (Tregs) have been an important subject of investigation in the biomedical field and our understanding of the mechanisms that drive their phenotype and function in health and disease has advanced tremendously. During the past few years it has become clear that Tregs are not a terminally differentiated population but show some degree of plasticity, and can, under specific environmental conditions, acquire the phenotype of effector T cells. In particular, recent works have highlighted the acquisition of a Th1-like phenotype by Tregs in several pathological environments. In this review we give an update on the concept of Treg plasticity and the advances in defining the molecular mechanisms that underlie the generation of Th1-like Tregs during an immune response and in different disease settings.</p>
</div>
</front>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Cell Mol Life Sci</journal-id>
<journal-id journal-id-type="iso-abbrev">Cell. Mol. Life Sci</journal-id>
<journal-title-group><journal-title>Cellular and Molecular Life Sciences</journal-title>
</journal-title-group>
<issn pub-type="ppub">1420-682X</issn>
<issn pub-type="epub">1420-9071</issn>
<publisher><publisher-name>Springer International Publishing</publisher-name>
<publisher-loc>Cham</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">28624966</article-id>
<article-id pub-id-type="pmc">7079789</article-id>
<article-id pub-id-type="publisher-id">2569</article-id>
<article-id pub-id-type="doi">10.1007/s00018-017-2569-y</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review</subject>
</subj-group>
</article-categories>
<title-group><article-title>Molecular mechanisms underlying Th1-like Treg generation and function</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Kitz</surname>
<given-names>Alexandra</given-names>
</name>
<address><phone>+1 203-737-4802</phone>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-9719-0028</contrib-id>
<name><surname>Dominguez-Villar</surname>
<given-names>Margarita</given-names>
</name>
<address><phone>+1 203-737-3399</phone>
<email>margarita.dominguez-villar@yale.edu</email>
</address>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<aff id="Aff1"><label>1</label>
<institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Departments of Neurology and Immunobiology,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</aff>
<aff id="Aff2"><label>2</label>
<institution-wrap><institution-id institution-id-type="ISNI">0000000419368710</institution-id>
<institution-id institution-id-type="GRID">grid.47100.32</institution-id>
<institution>Department of Neurology, Human and Translational Immunology Program,</institution>
<institution>Yale School of Medicine,</institution>
</institution-wrap>
300 George Street, New Haven, CT 06519 USA</aff>
</contrib-group>
<pub-date pub-type="epub"><day>17</day>
<month>6</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="ppub"><year>2017</year>
</pub-date>
<volume>74</volume>
<issue>22</issue>
<fpage>4059</fpage>
<lpage>4075</lpage>
<history><date date-type="received"><day>29</day>
<month>1</month>
<year>2017</year>
</date>
<date date-type="rev-recd"><day>22</day>
<month>5</month>
<year>2017</year>
</date>
<date date-type="accepted"><day>13</day>
<month>6</month>
<year>2017</year>
</date>
</history>
<permissions><copyright-statement>© Springer International Publishing AG 2017</copyright-statement>
<license><license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract id="Abs1"><p id="Par1">Since their ‘re-discovery’ more than two decades ago, FOXP3<sup>+</sup>
regulatory T cells (Tregs) have been an important subject of investigation in the biomedical field and our understanding of the mechanisms that drive their phenotype and function in health and disease has advanced tremendously. During the past few years it has become clear that Tregs are not a terminally differentiated population but show some degree of plasticity, and can, under specific environmental conditions, acquire the phenotype of effector T cells. In particular, recent works have highlighted the acquisition of a Th1-like phenotype by Tregs in several pathological environments. In this review we give an update on the concept of Treg plasticity and the advances in defining the molecular mechanisms that underlie the generation of Th1-like Tregs during an immune response and in different disease settings.</p>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd>Foxp3</kwd>
<kwd>Plasticity</kwd>
<kwd>Th1-Tregs</kwd>
<kwd>AKT</kwd>
<kwd>Therapy</kwd>
</kwd-group>
<funding-group><award-group><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100004755</institution-id>
<institution>EMD Serono</institution>
</institution-wrap>
</funding-source>
<award-id>Grant for Multiple Sclerosis Innovation</award-id>
<principal-award-recipient><name><surname>Dominguez-Villar</surname>
<given-names>Margarita</given-names>
</name>
</principal-award-recipient>
</award-group>
</funding-group>
<funding-group><award-group><funding-source><institution-wrap><institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000890</institution-id>
<institution>National Multiple Sclerosis Society</institution>
</institution-wrap>
</funding-source>
<award-id>Postdoctoral fellowship</award-id>
<principal-award-recipient><name><surname>Kitz</surname>
<given-names>Alexandra</given-names>
</name>
</principal-award-recipient>
</award-group>
</funding-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer International Publishing AG 2017</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body><sec id="Sec1"><title>Regulatory T cells control the immune system</title>
<p id="Par2">The immune system is armed with a variety of effector mechanisms to recognize and destroy foreign pathogens as well as with several peripheral tolerance processes to maintain tolerance to self. In this context, cells with regulatory capacity are crucial for maintaining immune homeostasis and peripheral tolerance, and they play an essential role in controlling autoimmune responses, allergies and limiting immunopathology [<xref ref-type="bibr" rid="CR1">1</xref>
–<xref ref-type="bibr" rid="CR6">6</xref>
]. While the spectrum of regulatory cells is wide and comprises many different cell types, naturally occurring regulatory T cells (Tregs) is the best studied population of cells with suppressive capacity [<xref ref-type="bibr" rid="CR6">6</xref>
]. They are generated in the thymus at the stage of CD4 single-positive thymocytes [<xref ref-type="bibr" rid="CR7">7</xref>
] as a separate cell lineage, and are thought to be enriched in self-reactive T-cell receptors (TCR), which is essential for maintenance of self-tolerance. As with the development of other cell lineages in the thymus [<xref ref-type="bibr" rid="CR8">8</xref>
, <xref ref-type="bibr" rid="CR9">9</xref>
], a specific requirement for TCR signaling is essential for the induction of its lineage specification transcription factor FOXP3 and Treg cell lineage commitment, and TCR specificity plays a critical role in this differentiation. Studies with TCR transgenic mice [<xref ref-type="bibr" rid="CR10">10</xref>
–<xref ref-type="bibr" rid="CR13">13</xref>
] and sequence analysis of polyclonal TCR repertoires from Tregs as compared to conventional T cells bearing a single transgene-encoded TCRβ chain [<xref ref-type="bibr" rid="CR14">14</xref>
–<xref ref-type="bibr" rid="CR16">16</xref>
] have led to the conclusion that Treg cell selection is probably instructed by TCRs with affinities for self-peptide–MHC complexes that are of an intermediate affinity between those that induce positive selection of non-Treg cells and those that mediate negative selection of self-reactive T cells. Medullary thymic epithelial cells (mTECs) are the major antigen-presenting cells in the thymus, and their phenotype and function are mediated in part by the transcription factor Aire, which regulates the expression of a multitude of genes, including antigens characteristic of fully differentiated cells in peripheral tissues, shaping the array of self-peptides presented by MHC and thus, the negative selection of effector T cells [<xref ref-type="bibr" rid="CR17">17</xref>
–<xref ref-type="bibr" rid="CR19">19</xref>
] and the positive selection of Tregs [<xref ref-type="bibr" rid="CR20">20</xref>
–<xref ref-type="bibr" rid="CR23">23</xref>
]. Additional signals needed for Treg differentiation in the thymus include cytokines such as IL-2 [<xref ref-type="bibr" rid="CR24">24</xref>
] and to a lesser extent IL-7 and IL-15 [<xref ref-type="bibr" rid="CR25">25</xref>
], and costimulatory molecules, among which, CD28 plays an important role in promoting natural Treg differentiation. Mice studies have shown that mice deficient in CD28 or its ligands CD80 and CD86 have significantly impaired Tregs [<xref ref-type="bibr" rid="CR26">26</xref>
, <xref ref-type="bibr" rid="CR27">27</xref>
], whereas CTLA-4 ablation results in a higher frequency of natural Tregs [<xref ref-type="bibr" rid="CR28">28</xref>
]. Both TCR and CD28 signaling trigger a myriad of intracellular signaling events that lead to the activation of transcription factors, including NFκB, which has been shown to be essential for natural Treg generation [<xref ref-type="bibr" rid="CR29">29</xref>
–<xref ref-type="bibr" rid="CR31">31</xref>
]. Lineage specificity is imprinted in early phases during development by the expression of FOXP3 [<xref ref-type="bibr" rid="CR32">32</xref>
] and by the induction of stable epigenetic changes [<xref ref-type="bibr" rid="CR33">33</xref>
–<xref ref-type="bibr" rid="CR35">35</xref>
].</p>
<p id="Par3">Tregs are characterized by the expression of the master transcription factor FOXP3 [<xref ref-type="bibr" rid="CR36">36</xref>
, <xref ref-type="bibr" rid="CR37">37</xref>
], the IL-2 receptor alpha chain, CD25 [<xref ref-type="bibr" rid="CR6">6</xref>
, <xref ref-type="bibr" rid="CR38">38</xref>
], and the low expression of the IL-7 receptor alpha chain, CD127 [<xref ref-type="bibr" rid="CR39">39</xref>
]. Many other markers have been described to be expressed in subpopulations of Tregs, arguing for heterogeneity within this population. IL-2 is an essential cytokine for Treg homeostasis and function. Tregs constitutively express high levels of CD25, and IL-2 is essential to preserve tolerance by influencing Treg homeostasis and activation [<xref ref-type="bibr" rid="CR40">40</xref>
, <xref ref-type="bibr" rid="CR41">41</xref>
]. In mice, knocking out or blocking IL-2 or CD25 results in Treg deficiency, impaired Treg development and reduced Treg function [<xref ref-type="bibr" rid="CR42">42</xref>
]. Furthermore, IL-2-driven signals through the JAK/STAT signaling pathway directly stabilize FOXP3 expression through STAT5 activation, subsequently driving their suppressive function [<xref ref-type="bibr" rid="CR43">43</xref>
, <xref ref-type="bibr" rid="CR44">44</xref>
]. Due to the absence of IL-2R signaling, IL-2 and CD25 knock out mice exhibit lethal autoimmunity caused by uncontrolled CD4<sup>+</sup>
T cell activation and proliferation [<xref ref-type="bibr" rid="CR45">45</xref>
, <xref ref-type="bibr" rid="CR46">46</xref>
]. Treg numbers are reduced in these mice [<xref ref-type="bibr" rid="CR47">47</xref>
] and co-transfer of functional Tregs can prevent autoimmunity [<xref ref-type="bibr" rid="CR48">48</xref>
], highlighting the importance of IL-2 signaling on Tregs for their role in controlling immune responses.</p>
<p id="Par4">In the setting of an immune response, CD4<sup>+</sup>
naïve T cells produce massive amounts of IL-2 and upregulate CD25, resulting in a self-enhancing loop that favors augmented CD4<sup>+</sup>
T cell activation, proliferation and polarization into T helper effector CD4<sup>+</sup>
T cells [<xref ref-type="bibr" rid="CR49">49</xref>
]. To counteract increased effector T cell activation, Tregs respond to IL-2 and activate mechanisms to regulate effector T cells to prevent uncontrolled pro-inflammatory and potentially harmful responses.</p>
</sec>
<sec id="Sec2"><title>FOXP3 as a master regulator of the Treg lineage</title>
<p id="Par5">FOXP3 is crucial for Treg development [<xref ref-type="bibr" rid="CR37">37</xref>
, <xref ref-type="bibr" rid="CR50">50</xref>
], function [<xref ref-type="bibr" rid="CR51">51</xref>
, <xref ref-type="bibr" rid="CR52">52</xref>
] and maintenance [<xref ref-type="bibr" rid="CR53">53</xref>
]. Thus, forced expression of FOXP3 in CD4<sup>+</sup>
T cells results in the acquisition of a regulatory phenotype, although it does not completely recapitulate Treg gene-specific signature [<xref ref-type="bibr" rid="CR54">54</xref>
, <xref ref-type="bibr" rid="CR55">55</xref>
], and experimental deletion of the <italic>FOXP3</italic>
gene in Tregs results in the loss of their suppressive capabilities [<xref ref-type="bibr" rid="CR32">32</xref>
, <xref ref-type="bibr" rid="CR37">37</xref>
, <xref ref-type="bibr" rid="CR53">53</xref>
]. Mutations in the <italic>FOXP3</italic>
gene leads to the human autoimmune immunodysregulation polyendocrinopathy enteropathy X-linked syndrome (IPEX), characterized by a loss of Treg function and severe autoimmunity. Patients with IPEX suffer from early-onset insulin-dependent diabetes mellitus, thyroiditis, massive lymphoproliferation, eczema, entheropathy and other autoimmune pathologies that are usually fatal during the first years of life [<xref ref-type="bibr" rid="CR56">56</xref>
, <xref ref-type="bibr" rid="CR57">57</xref>
]. Due to its essential role in maintaining Treg function and stability, it is not surprising that Foxp3 expression is tightly regulated. Transcription of <italic>Foxp3</italic>
gene has been shown to be modulated at the epigenetic level [<xref ref-type="bibr" rid="CR58">58</xref>
], and FOXP3 protein expression and stability may be controlled by post-translational modifications such as phosphorylation [<xref ref-type="bibr" rid="CR59">59</xref>
–<xref ref-type="bibr" rid="CR61">61</xref>
], acetylation [<xref ref-type="bibr" rid="CR62">62</xref>
, <xref ref-type="bibr" rid="CR63">63</xref>
] and ubiquitination [<xref ref-type="bibr" rid="CR64">64</xref>
, <xref ref-type="bibr" rid="CR65">65</xref>
], among others. Experiments with genetically engineered mouse models have shown that the genomic region of the <italic>Foxp3</italic>
locus has several conserved non-coding sequences (CNS1, CNS2, CNS3), which perform diverse functions in the regulation of <italic>Foxp3</italic>
transcription. CNS1 region contains binding sites for NFAT and AP-1, being important for peripheral generation of adaptive Tregs [<xref ref-type="bibr" rid="CR58">58</xref>
, <xref ref-type="bibr" rid="CR66">66</xref>
], while CNS3 plays a role in both natural and adaptive Treg generation and contains binding sites for transcription factors such as c-Rel [<xref ref-type="bibr" rid="CR58">58</xref>
]. Runx1-CBFβ complexes bind to CNS2 region to control <italic>Foxp3</italic>
expression and stability [<xref ref-type="bibr" rid="CR67">67</xref>
]. Moreover, epigenetic modifications of highly conserved regions within CNS in the <italic>Foxp3</italic>
locus are involved in the transcription of <italic>Foxp3</italic>
. Thus, CNS2 contains a conserved CpG island (TSDR region) that is highly demethylated in natural Tregs and hypermethylated in conventional CD4<sup>+</sup>
T cells [<xref ref-type="bibr" rid="CR34">34</xref>
, <xref ref-type="bibr" rid="CR68">68</xref>
, <xref ref-type="bibr" rid="CR69">69</xref>
], which determines <italic>Foxp3</italic>
expression and the stability of the Treg lineage [<xref ref-type="bibr" rid="CR33">33</xref>
, <xref ref-type="bibr" rid="CR69">69</xref>
, <xref ref-type="bibr" rid="CR70">70</xref>
]. This TSDR region has been widely used to distinguish <italic>bona fide</italic>
Tregs from T cell populations that can transiently upregulate FOXP3 upon activation [<xref ref-type="bibr" rid="CR71">71</xref>
]. Lastly, although FOXP3 is an essential transcription factor required by Tregs to maintain their phenotype and function, over the last few years several works in the literature have demonstrated that FOXP3 does not function alone but forms protein complexes with more than 300 potential partners [<xref ref-type="bibr" rid="CR72">72</xref>
]. Many of these partners are transcription factors such as, among others, NFAT, Gata-3, Smad, Runx1 and FOXO [<xref ref-type="bibr" rid="CR66">66</xref>
, <xref ref-type="bibr" rid="CR72">72</xref>
–<xref ref-type="bibr" rid="CR75">75</xref>
]. These transcription factors have been shown to be required to define the Treg cell phenotype and to establish their unique transcriptional program [<xref ref-type="bibr" rid="CR76">76</xref>
].</p>
<p id="Par6">Functionally, Tregs utilize cell–cell contact mechanisms and soluble factors to inhibit the activation of many different cell types. Thus, Tregs can suppress not only CD4<sup>+</sup>
and CD8<sup>+</sup>
T cells [<xref ref-type="bibr" rid="CR77">77</xref>
] but also other immune cells such as B lymphocytes [<xref ref-type="bibr" rid="CR78">78</xref>
–<xref ref-type="bibr" rid="CR81">81</xref>
], dendritic cells [<xref ref-type="bibr" rid="CR82">82</xref>
–<xref ref-type="bibr" rid="CR84">84</xref>
], monocytes [<xref ref-type="bibr" rid="CR85">85</xref>
, <xref ref-type="bibr" rid="CR86">86</xref>
], and NK cells [<xref ref-type="bibr" rid="CR87">87</xref>
, <xref ref-type="bibr" rid="CR88">88</xref>
], as well as non-immune cell types such as osteoclasts [<xref ref-type="bibr" rid="CR89">89</xref>
, <xref ref-type="bibr" rid="CR90">90</xref>
], underscoring the importance of this population to maintain immune homeostasis.</p>
<p id="Par7">FOXP3<sup>−</sup>
CD4<sup>+</sup>
T cells in the periphery can also acquire FOXP3 expression and suppressive function when they encounter their cognate antigen in the presence of TFGβ and IL-2 under certain environmental conditions. These Tregs are termed adaptive or induced Tregs (iTregs), and they show important epigenetic differences as compared to natural Tregs; however, we currently lack specific markers that distinguish both populations [<xref ref-type="bibr" rid="CR91">91</xref>
].</p>
<p id="Par8">Finally, FOXP3 expression also defines a population of CD8<sup>+</sup>
T cells with regulatory capacity both in mice and humans that seems to play a role in autoimmune, infectious and transplantation settings [<xref ref-type="bibr" rid="CR92">92</xref>
, <xref ref-type="bibr" rid="CR93">93</xref>
], although their origin and their function in the immune response in these disease scenarios is less studied than those of CD4<sup>+</sup>
Tregs. Interestingly, some early reports suggested that their suppressive function mainly depends on HLA-E recognition [<xref ref-type="bibr" rid="CR94">94</xref>
, <xref ref-type="bibr" rid="CR95">95</xref>
] and is mediated by IFNγ secretion [<xref ref-type="bibr" rid="CR96">96</xref>
, <xref ref-type="bibr" rid="CR97">97</xref>
], although the molecular mechanisms underlying this observation have not been examined in depth.</p>
</sec>
<sec id="Sec3"><title>Regulatory T cell plasticity</title>
<p id="Par9">Traditionally, Tregs have been considered as a stable cell lineage with strong suppressive capabilities and a terminally differentiated phenotype. But the idea of phenotype irreversibility has been recently challenged by a body of work demonstrating that Tregs are not a completely committed cell lineage, but can retain some degree of plasticity. This observation is not surprising in the context of an immune response, as multitude of works have clearly demonstrated that cell plasticity is an inherent property of most, if not all, immune cells that helps them adapt their phenotype and function to the changing environment [<xref ref-type="bibr" rid="CR98">98</xref>
–<xref ref-type="bibr" rid="CR102">102</xref>
]. In this regard, it is important to distinguish between functional plasticity and lineage instability. For the purpose of this review, we will consider functional plasticity as the capacity of Tregs to acquire a different phenotype due to environmental cues, anatomical location, among other factors, but maintaining either FOXP3 expression or Treg-specific epigenetic patterns. As such, three major plasticity events have been described with regards to Treg phenotype and/or function:</p>
<sec id="Sec4"><title>‘ex-FOXP3’ cells</title>
<p id="Par10">Cell-fate reporter mice have revealed that under certain inflammatory conditions, a small number of Tregs can lose FOXP3 expression and acquire effector-like phenotypes (‘ex-FOXP3’ cells), producing pro-inflammatory cytokines such as IL-2 and TNF and contributing to inflammation [<xref ref-type="bibr" rid="CR103">103</xref>
–<xref ref-type="bibr" rid="CR106">106</xref>
]. In some experimental conditions, these ex-FOXP3 cells appear to retain the Treg-specific epigenetic signature, potentially being able to be reconverted to FOXP3<sup>+</sup>
Tregs in the absence of the environmental cues that induced loss of FOXP3 expression [<xref ref-type="bibr" rid="CR107">107</xref>
]. The de-differentiation of Tregs into effector-like cells has also been observed in humans under several pathological settings [<xref ref-type="bibr" rid="CR108">108</xref>
–<xref ref-type="bibr" rid="CR110">110</xref>
].</p>
<p id="Par11">In relation to the loss of FOXP3 expression on Tregs, other studies have shown that FOXP3 degradation favors the secretion of cytokines such as IL-2, TNF and IFNγ and the decrease in suppressive function, especially in type I pathogenic settings [<xref ref-type="bibr" rid="CR64">64</xref>
]. The E3 ubiquitin ligases Stub1 and USP21 seem to play antagonistic roles in modulating the degradation of FOXP3 with Stub1 promoting degradation while USP21 stabilizing FOXP3 expression [<xref ref-type="bibr" rid="CR64">64</xref>
, <xref ref-type="bibr" rid="CR65">65</xref>
]. Pro-inflammatory cues such as cytokines and LPS signaling induce K48-linked polyubiquitination of FOXP3 by its interaction with Stub1, resulting in FOXP3 degradation, increased expression of IFNγ and reduced expression of characteristic Treg genes like CD25 and CTLA-4 [<xref ref-type="bibr" rid="CR64">64</xref>
] and subsequently disrupting Treg function. On the contrary, specific deletion of the ubiquitin ligase USP21 on mice Tregs induces an immune disorder characterized by increased expression of IFNγ by effector cells, and a Th1-like phenotype by Tregs. USP21 prevents FOXP3 degradation through deubiquination, thus stabilizing Treg phenotype and antagonizing the development of Th1-like Tregs [<xref ref-type="bibr" rid="CR65">65</xref>
]. While USP21 and Stub1 directly interact with FOXP3, the E3 ubiquitin ligase VHL indirectly regulates Th1-like Treg generation by increasing the expression of HIF-1α, which binds to the <italic>IFNG</italic>
promoter, increasing IFNγ production [<xref ref-type="bibr" rid="CR111">111</xref>
].</p>
</sec>
<sec id="Sec5"><title>Treg plasticity as a means of controlling immune responses and/or adapting to the tissue where they reside</title>
<p id="Par12">Several studies have demonstrated that Tregs utilize the transcription factor program of the population they are suppressing. Thus, Tregs that express T-BET efficiently suppress type 1 inflammation [<xref ref-type="bibr" rid="CR112">112</xref>
], IRF4 expression on Tregs is essential for controlling Th2 responses [<xref ref-type="bibr" rid="CR113">113</xref>
], and STAT3 is utilized by Tregs to control Th17 responses [<xref ref-type="bibr" rid="CR114">114</xref>
] in mouse models of inflammation.</p>
<p id="Par13">Recent studies in mice have also indicated that tissue-resident Tregs show a distinct gene expression pattern and TCR usage as compared to circulating Tregs [<xref ref-type="bibr" rid="CR115">115</xref>
–<xref ref-type="bibr" rid="CR117">117</xref>
]. For instance, the peroxisome proliferator-activated receptor gamma (PPARγ) was identified as the characteristic transcription factor utilized by fat tissue-resident Tregs to maintain their unique phenotype [<xref ref-type="bibr" rid="CR115">115</xref>
]. Interestingly, PPARγ is predominantly expressed on adipocytes, where its function is to regulate adipocyte differentiation and to mediate glucose metabolism [<xref ref-type="bibr" rid="CR118">118</xref>
]. This suggests that tissue-specific Treg phenotypes are also driven by tissue-specific transcription factors, introducing an additional type of plasticity. Similarly, other studies have identified roles for Treg cells in muscle repair [<xref ref-type="bibr" rid="CR119">119</xref>
, <xref ref-type="bibr" rid="CR120">120</xref>
], regulation of skin homeostasis, and prevention of skin infections [<xref ref-type="bibr" rid="CR121">121</xref>
]. Both muscle- and skin-derived Tregs show a differential gene expression pattern as compared to blood- and fat-derived Tregs, indicating that Tregs might adapt their phenotype and function to the tissue they populate, a process that is probably mediated by the specific tissue microenvironment.</p>
</sec>
<sec id="Sec6"><title>Th-like Tregs</title>
<p id="Par14">Lastly, under certain inflammatory settings, some Tregs can acquire an effector T helper (Th)-like phenotype with the capacity to express pro-inflammatory cytokines, mainly IFNγ (Th1-like Tregs), IL-17 (Th17-like Tregs) and IL-13 (Th2-like Tregs), and lose suppressive capacities while maintaining FOXP3 expression. In this regard, little is known about the phenotype and function of Th17-like Tregs under inflammatory conditions. For instance, when Tregs are stimulated in vitro in the presence of dectin-1-activated dendritic cells (DC), they upregulate RORγt and express IL-17 [<xref ref-type="bibr" rid="CR122">122</xref>
]. Interestingly, Th17-like Tregs have been observed in vivo in humans under physiological conditions [<xref ref-type="bibr" rid="CR123">123</xref>
, <xref ref-type="bibr" rid="CR124">124</xref>
] and in mice, preferentially located in the intestine [<xref ref-type="bibr" rid="CR125">125</xref>
]. Human Th17-like Tregs seem to maintain their suppressive capacity despite IL-17 expression in healthy individuals [<xref ref-type="bibr" rid="CR123">123</xref>
, <xref ref-type="bibr" rid="CR124">124</xref>
], and they can be induced in vitro by stimulation of Tregs in the presence of IL-6 and IL-1β [<xref ref-type="bibr" rid="CR123">123</xref>
]. These cells could have pathogenic potential, contributing to mucosal disease and being involved in the development of colon cancer [<xref ref-type="bibr" rid="CR110">110</xref>
, <xref ref-type="bibr" rid="CR126">126</xref>
, <xref ref-type="bibr" rid="CR127">127</xref>
] and inflammatory bowel disease [<xref ref-type="bibr" rid="CR128">128</xref>
]. In this respect, Saito et al. have recently observed that some tumors from patients with colorectal cancer contain an increased frequency of Foxp3<sup>low</sup>
Tregs with increased IL-17 secretion and decreased suppressive function as compared to peripheral blood, and this group of patients seems to have a better prognosis than those who do not display the increase in Th17-like Tregs [<xref ref-type="bibr" rid="CR110">110</xref>
]. Other recent reports have described the presence of Th17-like Tregs in the skin of psoriasis [<xref ref-type="bibr" rid="CR129">129</xref>
] as well as arthritis [<xref ref-type="bibr" rid="CR130">130</xref>
] patients.</p>
<p id="Par15">Th2-like Tregs have been recently observed in a mouse model of food allergy, and they are increased in frequency in children with milk allergy as compared to healthy donors or children with other food allergies. These Th2-like Tregs are characterized by an increased expression of the transcription factors GATA3 and IRF4 and increased secretion of IL-4 and IL-13 [<xref ref-type="bibr" rid="CR131">131</xref>
, <xref ref-type="bibr" rid="CR132">132</xref>
]. The production of both cytokines by Tregs directly contributes to disease, as specific disease amelioration is observed upon Treg cell-specific deletion of IL-4 and IL-13 [<xref ref-type="bibr" rid="CR132">132</xref>
]. Moreover, viral infection with the respiratory syncytial virus (RSV), which is known to increase the risk for asthma in adults when infection occurs early in life, induces a Th2-like inflammation in the lung, which promotes a Th2-like effector phenotype in Treg cells and a loss of suppressive function [<xref ref-type="bibr" rid="CR131">131</xref>
]. In vitro, Th2-like Tregs can be polarized by the stimulation of Tregs in the presence of IL-4 and IL-13 [<xref ref-type="bibr" rid="CR131">131</xref>
, <xref ref-type="bibr" rid="CR132">132</xref>
].</p>
<p id="Par16">Similarly, we and others have shown that Tregs from healthy individuals stimulated in vitro in the presence of IL-12 acquire a Th1-like phenotype characterized by the secretion of IFNγ, upregulation of T-BET and other Th1-related markers, such as CXCR3 and CCR5, both in mice and humans [<xref ref-type="bibr" rid="CR68">68</xref>
, <xref ref-type="bibr" rid="CR133">133</xref>
]. Despite the maintained expression of FOXP3, these Th1-like Tregs are defective in suppressive capacity as compared to Tregs, although they retain some degree of inhibitory function in most cases [<xref ref-type="bibr" rid="CR68">68</xref>
, <xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR134">134</xref>
]. Several reports have described the in vivo generation of Th1-like Tregs in inflammatory environments such as <italic>Toxoplasma gondii</italic>
infection [<xref ref-type="bibr" rid="CR135">135</xref>
], neurotropic hepatitis virus [<xref ref-type="bibr" rid="CR136">136</xref>
] and in patients with autoimmune diseases such as relapsing-remitting Multiple sclerosis [<xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR137">137</xref>
] and type 1 diabetes [<xref ref-type="bibr" rid="CR134">134</xref>
].</p>
<p id="Par17">In this review we give an update on the molecular mechanisms responsible for Th1-like Treg generation focusing on two Treg plasticity aspects: the acquisition of a Th1-suppressing phenotype to control type 1 immune responses, and the acquisition of an effector-like phenotype characterized by their inflammatory nature. We also review recent literature on the role of Th1-like Tregs in several pathological settings such as autoimmune diseases, infections and cancer, and the potential modulation of Treg plasticity as a therapeutic strategy in human disease.</p>
</sec>
</sec>
<sec id="Sec7"><title>Suppressive Th1-like Tregs: a method to control specific immune responses</title>
<p id="Par18">During the past years, it has become clear that Treg function is a finely modulated process during the extent of an immune response and is very much dependent on the anatomical location of the occurring reaction, as well as the type of immune response they are controlling. In this regard, it has been observed that Tregs acquire the expression of the master transcription factor that is similar to the effector T cell population or type of immune response that they are suppressing. Thus, Tregs co-opt for IRF4 to inhibit Th2 responses [<xref ref-type="bibr" rid="CR113">113</xref>
] and STAT3 to control Th17 pathology [<xref ref-type="bibr" rid="CR114">114</xref>
], while T-BET expression acquisition by Tregs is necessary for the control of type 1 inflammation in vivo [<xref ref-type="bibr" rid="CR112">112</xref>
].</p>
<p id="Par19">In mice, Koch et al. demonstrated that a Treg subpopulation expressing CXCR3 (a surface marker preferentially expressed on Th1 CD4<sup>+</sup>
T cells) is present in the circulation of wild-type animals [<xref ref-type="bibr" rid="CR112">112</xref>
]. CXCR3 expression is regulated by the transcription factor T-BET [<xref ref-type="bibr" rid="CR138">138</xref>
]. T-BET expression in turn is further induced in Tregs during type-I inflammation, subsequently resulting in an enrichment of T-BET<sup>+</sup>
Tregs that is necessary to control T cell responses during <italic>Mycobacterium</italic>
sp. infection [<xref ref-type="bibr" rid="CR112">112</xref>
]. Although T-BET is classically defined as a Th1-driving transcription factor controlling the expression of IFNγ, T-BET<sup>+</sup>
Tregs do not seem to express IFNγ in this model; this is likely to be due to the absence of IL-12 receptor beta 2 subunit (<italic>IL12RB2</italic>
) expression and the lack of IL-12-induced signaling pathways [<xref ref-type="bibr" rid="CR139">139</xref>
]. The differentiation of Tregs into Th1-suppressing Tregs is likely to be tightly controlled by cytokines in the microenvironment. In the case of a type 1 immune response, antigen presenting cells (APCs) and other cells from the innate immune system, such as NK cells and macrophages, release Th1-associated cytokines, IL-12, TNFα and IFNγ, which induce a Th1 phenotype on CD4<sup>+</sup>
effector T cells. These cytokines also shape the phenotype and function of Tregs.</p>
<p id="Par20">TNFα can trigger pro- and anti-inflammatory pathways in Tregs. A subset of both murine and human Tregs express the TNF receptor 2 (TNFR2) [<xref ref-type="bibr" rid="CR140">140</xref>
, <xref ref-type="bibr" rid="CR141">141</xref>
]. TNFα stimulation induces, synergistically with IL-2, the expression of other members of the TNFR superfamily such as 4-1BB and OX40 [<xref ref-type="bibr" rid="CR142">142</xref>
]. Interestingly, OX40 (CD134; TNFRSF4) has recently been shown to induce Treg activation and suppressive function [<xref ref-type="bibr" rid="CR143">143</xref>
]. Furthermore, in vitro experiments have demonstrated the induction of Treg proliferation and promotion of Treg stability upon OX40 engagement via APC-mediated activation and stimulation with OX40 ligand (OX40L). TNFα stimulation increases OX40 expression and promotes Treg suppressive function [<xref ref-type="bibr" rid="CR143">143</xref>
, <xref ref-type="bibr" rid="CR144">144</xref>
]. During type I inflammation, Th1 effector T cells as well as macrophages release a large amount of TNFα. TNFα in turn is essential to stabilize Treg function in a mouse model of colitis [<xref ref-type="bibr" rid="CR145">145</xref>
] as well as murine autoimmune diabetes [<xref ref-type="bibr" rid="CR146">146</xref>
]. Mediating the accumulation of suppressive Tregs in a TNFα-dependent manner poses a potential feedback mechanism to regulate strong type I inflammatory responses. On the other hand, TNFα can inflict negative effects on Treg stability and function. For instance, Valencia et al. demonstrated in vitro that the addition of TNFα in concentrations of 50 ng/ml inhibits Treg suppression and it is accompanied by decreased FOXP3 expression in a TNFR2-dependent manner [<xref ref-type="bibr" rid="CR147">147</xref>
]. In rheumatoid arthritis, TNFα negatively modulates Treg suppressive function [<xref ref-type="bibr" rid="CR147">147</xref>
] and dephosphorylates FOXP3 [<xref ref-type="bibr" rid="CR61">61</xref>
]. Additionally, anti-TNFα therapy induced Tregs in rheumatoid arthritis patients [<xref ref-type="bibr" rid="CR148">148</xref>
, <xref ref-type="bibr" rid="CR149">149</xref>
]. However, Zhong et al. observed inhibitory effects of TNFα mainly on Helios<sup>low</sup>
Tregs [<xref ref-type="bibr" rid="CR150">150</xref>
], suggesting that the observed differential effects of TNFα might be highly dependent on the specific Treg subpopulation and/or the inflammatory milieu.</p>
<p id="Par21">IFNγ is mainly released by NK cells and Th1 effector cells in the context of type-I inflammation. In Tregs, IFNγ increases <italic>TBET</italic>
expression in a STAT1-dependent manner resulting in induction of <italic>IL12RB2</italic>
expression [<xref ref-type="bibr" rid="CR139">139</xref>
]. The impact of IFNγ on Tregs is thus dichotomic as the upregulation of <italic>IL12RB2</italic>
renders Tregs susceptible to IL-12 signaling and subsequent polarization into Th1-like Tregs. However, during type-I immune responses, IFNγ fosters the polarization of Th1-suppressing Tregs [<xref ref-type="bibr" rid="CR112">112</xref>
]. As IFNγ signaling induces <italic>TBET</italic>
expression, IFNγ released by Th1 effector CD4<sup>+</sup>
T cells can act as a feedback mechanism to control type-I immune responses through expansion of Th1-suppressing Tregs and maintenance of high levels of T-BET expression. In regards to IL-12 signaling on Tregs, some reports in the literature suggested that in steady state conditions, Tregs expressed much lower levels of the <italic>IL12RB2</italic>
subunit mRNA as compared to FOXP3<sup>−</sup>
T cells [<xref ref-type="bibr" rid="CR139">139</xref>
], suggesting that these cells would not be responsive to IL-12 ex vivo. IFNγ induces <italic>IL12RB2</italic>
in a STAT4-dependent manner in both murine and human Tregs in vitro [<xref ref-type="bibr" rid="CR139">139</xref>
, <xref ref-type="bibr" rid="CR143">143</xref>
]. Subsequent exposure of IFNγ-primed Tregs to IL-12 renders Tregs dysfunctional and favors the polarization of Th1-like IFNγ-producing Tregs leading to a disrupted regulation of type-I inflammatory responses [<xref ref-type="bibr" rid="CR151">151</xref>
]. However, the upregulation of IFNγ at RNA and protein levels by human and mice Tregs upon ex vivo stimulation in the presence of IL-12 has been widely demonstrated [<xref ref-type="bibr" rid="CR68">68</xref>
, <xref ref-type="bibr" rid="CR133">133</xref>
–<xref ref-type="bibr" rid="CR135">135</xref>
]. IL-12 induces IFNγ-producing Th1-like Tregs that in addition show inhibited proliferative capacities, reduced suppressive function and expression of CD25 [<xref ref-type="bibr" rid="CR113">113</xref>
, <xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR134">134</xref>
]. In agreement with these results, recent data suggest that human Tregs do express <italic>IL12RB2</italic>
at the RNA level in the steady state [<xref ref-type="bibr" rid="CR152">152</xref>
], which would explain the rapid increase in <italic>IFNG</italic>
expression upon IL-12 stimulation. Thus, the balance between differentiation into Th1-suppressing or Th1-like Tregs might be somewhat different between mice and humans and might not be controlled by the expression of <italic>IL12RB2</italic>
and sensitivity to IL-12, but rather by the amount and availability of IL-12 in the microenvironment and/or the duration of IL-12 signaling (Fig. <xref rid="Fig1" ref-type="fig">1</xref>
). In this regard, a subpopulation of Tregs expressing OX40, which can be induced by TNFα, has been found to differentiate into Th1-suppressing Tregs and OX40 to compete for IL-12 [<xref ref-type="bibr" rid="CR143">143</xref>
], unraveling another possible mechanism that drives Tregs into different Th1-associated phenotype and functions.<fig id="Fig1"><label>Fig. 1</label>
<caption><p>Functional differentiation of Treg cells into Th1-suppressing and Th1-like Tregs. FOXP3<sup>+</sup>
Tregs upregulate T-BET expression upon type I inflammatory stimuli such as IFNγ in a STAT1-dependent manner. T-BET<sup>+</sup>
FOXP3<sup>+</sup>
Tregs retain their suppressive function and contribute to resolution of type I inflammation. Additional or subsequent exposure to IL-12 drives Tregs to express T-BET and release IFNγ. IFNγ-producing Tregs either contribute to resolution of type I inflammation (Th1-suppressing) or lose suppressive function and fail to efficiently control autoimmune responses (Th1-like Tregs)</p>
</caption>
<graphic xlink:href="18_2017_2569_Fig1_HTML" id="MO1"></graphic>
</fig>
</p>
</sec>
<sec id="Sec8"><title>Th1-like Treg signaling</title>
<p id="Par22">In humans, in vitro stimulation of Tregs with IL-12 induces a Th1-like Treg phenotype with upregulation of T-BET, CXCR3, CCR5 and IFNγ expression [<xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR151">151</xref>
]. In contrast to mice studies [<xref ref-type="bibr" rid="CR139">139</xref>
], human Treg stimulation in the presence of IFNγ does not induce a Th1-like phenotype, with IL-12 efficiently inducing <italic>IFNG</italic>
gene expression as soon as 24 h after stimulation in vitro ([<xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR153">153</xref>
] and unpublished data). While FOXP3 expression and the methylation status of the TSDR locus remain unaffected by IL-12 exposure, Th1-like Tregs diminish their suppressive function in in vitro co-cultures with Treg-depleted CD4<sup>+</sup>
T cells. In relation to the signaling pathways that drive the generation of Th1-like Tregs in humans, we recently defined the PI3K/AKT/FOXO pathway as a major axis involved in IFNγ production by Tregs [<xref ref-type="bibr" rid="CR153">153</xref>
]. PI3K/AKT is a critical signaling node in all eukaryotic cells and the AKT family of proteins is one of the most versatile and important kinases in human physiology and disease. The AKT family of proteins comprises 3 mammalian isoforms (AKT1, AKT2 and AKT3), encoded by separate genes [<xref ref-type="bibr" rid="CR154">154</xref>
]. AKT is activated downstream of PI3K, which can be triggered by multiple stimuli such as T cell receptor (TCR) engagement [<xref ref-type="bibr" rid="CR155">155</xref>
], costimulatory molecules such as CD28 [<xref ref-type="bibr" rid="CR156">156</xref>
], cytokine receptors [<xref ref-type="bibr" rid="CR153">153</xref>
, <xref ref-type="bibr" rid="CR157">157</xref>
], G protein-coupled receptors [<xref ref-type="bibr" rid="CR158">158</xref>
] and insulin [<xref ref-type="bibr" rid="CR159">159</xref>
], among others. AKT is fully activated by phosphorylation at both Ser 473 by mTORC2 [<xref ref-type="bibr" rid="CR160">160</xref>
], and at Thr 308 by PI3K-activated PDK1 [<xref ref-type="bibr" rid="CR161">161</xref>
]. Although phosphorylation at Ser 473 is necessary for full activation, once triggered by growth factors, phosphorylation at this residue by mTORC2 targets AKT for degradation by the ubiquitin system [<xref ref-type="bibr" rid="CR162">162</xref>
]. Once activated, AKT is able to phosphorylate and activate a myriad of downstream substrates, influencing diverse cellular and physiological processes such as cell cycle progression, cell growth, cell differentiation, cell survival, metabolism, angiogenesis and motility [<xref ref-type="bibr" rid="CR163">163</xref>
–<xref ref-type="bibr" rid="CR165">165</xref>
]. One of these multiple AKT targets is the FOXO family of transcription factors, which has been widely involved in Treg development and function in mice studies [<xref ref-type="bibr" rid="CR73">73</xref>
, <xref ref-type="bibr" rid="CR166">166</xref>
, <xref ref-type="bibr" rid="CR167">167</xref>
]. The PI3K/AKT/FOXO axis is tightly regulated by the function of several phosphatases that act at different levels of the pathway, among which, PTEN inhibits PI3K by dephosphorylating PI(3,4,5)P<sub>3</sub>
to PI(4,5)P<sub>2</sub>
and PHLPP phosphatases dephosphorylate AKT kinases [<xref ref-type="bibr" rid="CR168">168</xref>
].</p>
<p id="Par23">IFNγ<sup>+</sup>
Tregs isolated from healthy individuals show an increased expression of AKT1 and decreased expression of FOXO3, AKT3 and PTEN. Interestingly, using IL-12 as an in vitro model for Th1-like Treg generation, it is observed that IL-12 directly induces Th1 polarization by activation of the PI3K/AKT/FOXO1/3 pathway as measured by phosphorylation of AKT at residue Thr 308 and FOXO1/3 at Ser 319 [<xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR153">153</xref>
]. Despite the well known involvement of AKT in cell survival, in vitro experiments did not show increased Th1-like Treg survival as compared to control Tregs [<xref ref-type="bibr" rid="CR153">153</xref>
], although the in vivo role of this pathway in promoting Th1-like Treg cell survival remains to be elucidated. Previous studies had highlighted the importance of the PI3K/AKT axis in Treg development [<xref ref-type="bibr" rid="CR169">169</xref>
, <xref ref-type="bibr" rid="CR170">170</xref>
] and function [<xref ref-type="bibr" rid="CR171">171</xref>
], demonstrating that diminished AKT activation is necessary for human Tregs to foster suppressive capacities [<xref ref-type="bibr" rid="CR171">171</xref>
]. The importance of the PI3K/AKT/FOXO1/3 pathway is further highlighted by a series of in vitro experiments where interference with the pathway by either pharmacological activation of PI3K or AKT1, or inhibition of PTEN or FOXO1/3 resulted in increased expression of IFNγ and T-BET as well as reduced suppressive function [<xref ref-type="bibr" rid="CR153">153</xref>
]. These data are in agreement with some recent works demonstrating that PI3K and PTEN are essential for Treg stability in vivo in mouse Tregs [<xref ref-type="bibr" rid="CR172">172</xref>
, <xref ref-type="bibr" rid="CR173">173</xref>
]. PTEN stabilizes the metabolic balance between glycolysis and mitochondrial fitness, and PTEN-deficient Tregs show increased phosphorylation of AKT and higher expression of activation markers. In these mice, activated memory-effector T cells produce high amounts of IFNγ and upregulate CXCR3, underscoring the importance of the PTEN/AKT axis to stabilize Treg phenotype and modulate Treg-mediated control of type 1 immune responses [<xref ref-type="bibr" rid="CR172">172</xref>
]. Tregs deficient in PTEN show increased PI3K activity and downregulate the expression of CD25 and FOXP3 which leads to reduced suppressive capacity further demonstrating the relevance of the PI3K/AKT/FOXO1/3 pathway for Treg homeostasis and function [<xref ref-type="bibr" rid="CR173">173</xref>
]. FOXO1 has also been involved in the stability and function of Tregs, as FOXO<sup>−/−</sup>
Tregs display an increase in IFNγ expression and a pro-inflammatory phenotype, and mice with Treg-specific deletion of FOXO1 succumb to a fatal autoimmune disorder similar in severity to that observed in FOXP3 deficient mice [<xref ref-type="bibr" rid="CR73">73</xref>
] (Fig. <xref rid="Fig2" ref-type="fig">2</xref>
).<fig id="Fig2"><label>Fig. 2</label>
<caption><p>The PI3K/AKT/FOXO pathway is a key regulator of Th1-like Treg differentiation. Upon T cell activation via the T cell receptor or cytokine receptors, the phosphatidylinositol 3-kinase (PI3K) phosphorylates PI(4,5)P<sub>2</sub>
to PI(3,4,5)P<sub>3</sub>
which in turn recruits PDK1. PTEN counteracts PI3K activity by dephosphorylating PI(3,4,5)P<sub>3</sub>
to PI(4,5)P<sub>2</sub>
. PDK1 phosphorylates AKT at Thr 308. Additional phosphorylation of AKT at Ser 473 by mTORC2, activates AKT to phosphorylate FOXO transcription factors, which promotes their nuclear export. FOXO1/3 are essential to stabilize FOXP3 expression in Tregs. In the case of Th1-like Tregs, AKT phosphorylation is enhanced resulting in increased FOXO1/3 nuclear export, which enables other signaling events to trigger <italic>TBET</italic>
and <italic>IFNG</italic>
gene expression</p>
</caption>
<graphic xlink:href="18_2017_2569_Fig2_HTML" id="MO2"></graphic>
</fig>
</p>
<p id="Par24">Interestingly, AKT isoforms exhibit differential functions on the context of Th1-like Treg polarization [<xref ref-type="bibr" rid="CR153">153</xref>
]. While AKT1 is upregulated in IFNγ-producing Th1-like Tregs and AKT1 blockade can prevent Th1-like Treg polarization [<xref ref-type="bibr" rid="CR153">153</xref>
, <xref ref-type="bibr" rid="CR171">171</xref>
], AKT3 silencing was sufficient to induce IFNγ production by human Tregs [<xref ref-type="bibr" rid="CR153">153</xref>
]. Other studies have suggested non-overlapping functions of AKT isoforms in the context of cancer biology and vascular disease [<xref ref-type="bibr" rid="CR154">154</xref>
, <xref ref-type="bibr" rid="CR165">165</xref>
, <xref ref-type="bibr" rid="CR174">174</xref>
]. Moreover, in the context of autoimmunity, a recent study has attributed AKT3 a protective role in EAE development in mice [<xref ref-type="bibr" rid="CR175">175</xref>
].</p>
<p id="Par25">Besides the PI3K/AKT/FOXO pathway, gene expression analysis of human IFNγ<sup>+</sup>
and IFNγ<sup>−</sup>
Tregs has shown that other signaling pathways are differentially expressed in Th1-like Tregs, suggesting that they could also be involved in Th1-like Treg generation, although their functional relevance remains to be determined [<xref ref-type="bibr" rid="CR153">153</xref>
].</p>
</sec>
<sec id="Sec9"><title>Th1-like Tregs in autoimmunity</title>
<p id="Par26">In regards to autoimmune pathologies, several works in the literature have defined the presence of Th1-like Tregs in patients with various diseases, such as Multiple Sclerosis (MS) [<xref ref-type="bibr" rid="CR133">133</xref>
, <xref ref-type="bibr" rid="CR153">153</xref>
], type 1 diabetes (T1D) [<xref ref-type="bibr" rid="CR134">134</xref>
], de novo autoimmune hepatitis in patients with liver transplant [<xref ref-type="bibr" rid="CR176">176</xref>
] and in inflammatory bowel disease [<xref ref-type="bibr" rid="CR177">177</xref>
–<xref ref-type="bibr" rid="CR179">179</xref>
] (IBD). We described some years ago that untreated relapsing-remitting (RR) MS patients display an increased frequency of Th1-like Tregs in peripheral blood. These Tregs express increased levels of T-BET, CXCR3, CCR5, and IFNγ and decreased levels of TGFβ, and CTLA-4, being defective in function [<xref ref-type="bibr" rid="CR133">133</xref>
]. Interestingly, IFNγ is involved in the decreased suppressive capacity observed in Tregs from RRMS patients, as IFNγ blockade in ex vivo co-cultures of Tregs and Treg-depleted CD4<sup>+</sup>
T cells from patients with MS, significantly increased their suppressive function. Moreover, the elevated frequency of Th1-like Tregs in RRMS patients is due, at least in part, to the in vivo activated status of the AKT/FOXO pathway as compared to Tregs from healthy individuals, with increased expression of phosphorylated AKT (Thr 308) and FOXO1/3 (Ser 319) [<xref ref-type="bibr" rid="CR153">153</xref>
]. Therefore, blockade of PI3K activation in ex vivo stimulated Tregs from MS patients decreased the frequency of IFNγ-producing Tregs and increased their suppressive capacit<italic>y</italic>
. The presence of Th1-like Tregs has also been observed in Tregs infiltrating the CNS in vivo, during EAE development, utilizing a FOXP3 knock-in mouse model. In this model, antigen-specific Tregs and effector T cells were traced by MOG-specific tetramers at different points after EAE induction [<xref ref-type="bibr" rid="CR137">137</xref>
]. Upon EAE induction, MOG-specific Tregs were not capable of suppressing CNS-infiltrating MOG-specific T cells in vivo and in vitro and prevent disease onset, and secreted IFNγ at the onset and peak of the disease, decreasing the amount during the recovery phase and increasing IL-10 secretion [<xref ref-type="bibr" rid="CR137">137</xref>
].</p>
<p id="Par27">Similarly, patients with T1D display an increased frequency of Th1-like Tregs as compared to healthy individuals [<xref ref-type="bibr" rid="CR134">134</xref>
] that can be observed in in vitro expanded or in ex vivo isolated Tregs. Similar to the observation made with MS patients, Th1-like Tregs in T1D patients contained both Helios<sup>+</sup>
and Helios<sup>−</sup>
Tregs. Although initially thought to be a marker of thymus-derived Tregs [<xref ref-type="bibr" rid="CR180">180</xref>
], contradictory works have occluded the use of this marker to differentiate natural versus adaptive Tregs [<xref ref-type="bibr" rid="CR181">181</xref>
–<xref ref-type="bibr" rid="CR184">184</xref>
]. In vivo, a recent work has demonstrated that in the pre-diabetes phase in the NOD mouse model there is an increased frequency of Th1-like Tregs in the draining lymph nodes, characterized by the expression of T-BET, CXCR3, ICOS and IFNγ. These CXCR3<sup>+</sup>
ICOS<sup>+</sup>
Th1-like Tregs, however, retain some degree of suppressive capacity in vivo in adoptive transfer experiments [<xref ref-type="bibr" rid="CR185">185</xref>
].</p>
<p id="Par28">Tregs are increased in frequency in inflamed intestinal tissue in animal models and patients with IBD [<xref ref-type="bibr" rid="CR178">178</xref>
, <xref ref-type="bibr" rid="CR179">179</xref>
] and most of them express IFNγ and IL-17, potentially enhancing inflammation or inhibiting regulation. But contradictory results have been found in in vivo models of colitis with regards to the protective or pathogenic role of Th1-like Tregs in this setting [<xref ref-type="bibr" rid="CR177">177</xref>
–<xref ref-type="bibr" rid="CR179">179</xref>
]. While antigen-specific IFNγ<sup>+</sup>
Tregs were able to prevent colitis in an adoptive transfer model with flagellin-specific Tregs [<xref ref-type="bibr" rid="CR178">178</xref>
], FOXO<sup>−/−</sup>
Tregs, which show a Th1-like phenotype, we unable to prevent diseases in a colitis model, with IFNγ being involved on the Treg defect in function, as FOXO<sup>−/−</sup>
IFNG<sup>−/−</sup>
double knock-out mice were able to partially recover from the wasting syndrome [<xref ref-type="bibr" rid="CR73">73</xref>
].</p>
</sec>
<sec id="Sec10"><title>Th1-like Tregs in infections and tumor environments</title>
<p id="Par29">Both Th1-suppressing and Th1-like Tregs have been described in several models of infection and tumor environments, with each of the two populations contributing to disease manifestations and outcome. Th1-suppressing Tregs, characterized by elevated levels of T-BET and CXCR3 but not IFNγ, are induced in a model of type I inflammation with <italic>Leishmania major</italic>
and <italic>Mycobacterium tuberculosis</italic>
infections in mice [<xref ref-type="bibr" rid="CR112">112</xref>
]. T-BET-expressing Tregs accumulated at the site of infection, balanced Th1 inflammatory responses and maintained their homeostasis and function. In other infection models, Th1-like Tregs gained the ability to express IFNγ resulting in differential clinical outcomes of the infection models. Thus, during <italic>T. gondii</italic>
infection, T-BET and IFNγ expression were triggered in Tregs while FOXP3 expression declined coinciding with strong immunopathology and subsequent lethal disease progression [<xref ref-type="bibr" rid="CR135">135</xref>
]. Although IFNγ is considered to be a highly pro-inflammatory cytokine, Hall et al. reported the rise of IFNγ<sup>+</sup>
Tregs that were able to suppress Th1 effector T cells and limit effector T cell responses to <italic>T. gondii</italic>
infection [<xref ref-type="bibr" rid="CR186">186</xref>
]. Along this line, IFNγ<sup>+</sup>
Tregs in a colitis model retained suppressive function in vitro and inhibited the induction of colitis by microbiota antigen-specific T cells in vivo [<xref ref-type="bibr" rid="CR113">113</xref>
]. IFNγ<sup>+</sup>
Th1-suppressing Tregs were also observed in a chronic corona-virus-induced encephalomyelitis model during both acute and chronic phases of infection [<xref ref-type="bibr" rid="CR136">136</xref>
]. Again, Th1-suppressing Tregs produced IFNγ and retained their function in this model, being more likely to contribute to diminishing immunopathology. Koenecke et al., further demonstrated the protective role of IFNγ-producing Tregs as these cells appear in both <italic>Listeria monocytogenes infection</italic>
and in acute graft-versus-host disease (GVHD). Ablation of IFNγ in Tregs resulted in the development of lethal GVHD undermining the importance of IFNγ-production by Tregs to prevent GVHD [<xref ref-type="bibr" rid="CR187">187</xref>
].</p>
<p id="Par30">A recent study identified differential surface expression of OX40 to coincide with IFNγ-expression and Treg function in Tregs isolated from liver tissue from human hepatocellular carcinoma and cirrhosis patients [<xref ref-type="bibr" rid="CR143">143</xref>
]. These data suggest that OX40 expression efficiently separates Th1-like (OX40<sup>−</sup>
) Tregs with IFNγ expression and reduced suppressive function from Th1-suppressing (OX40<sup>+</sup>
) Tregs. In this study, cirrhosis tissue and tumor microenvironments favor the accumulation of OX40<sup>+</sup>
Th1-suppressing Tregs, whereas OX40<sup>−</sup>
Th1-like Tregs preferentially accumulate in non-cirrhotic chronic HCV-associated liver tissue. OX40 stimulation can abolish Treg function and thus it has been investigated as a potential antitumor target [<xref ref-type="bibr" rid="CR188">188</xref>
]. Furthermore, recent data in patients with colorectal cancer have shown that a small percentage of Tregs from either peripheral blood or infiltrating the tumor express IFNγ at similar levels, but the study lacks healthy individuals for absolute comparison [<xref ref-type="bibr" rid="CR110">110</xref>
].</p>
<p id="Par31">Taken together, these data demonstrate that Th1-suppressive and Th1-like regulatory T cells appear in a variety of infections and tumor environments. Whereas the expression of the transcription factor T-BET seems to be a characteristic feature in all models, additional differentiation and expression of IFNγ can either be connected with protective or pro-inflammatory function in these disease settings.</p>
</sec>
<sec id="Sec11"><title>Treg plasticity as a potential therapeutic strategy</title>
<p id="Par32">Tregs represent a major barrier to effective immune responses in antitumor immunity, as well as in chronic viral infections. The identification of pathways that maintain Treg cell stability or that induce Th-like effector functions on Tregs could potentially present important novel therapeutic approaches to undermine intratumoral Tregs or Tregs in chronic infections and to enhance disease clearance.</p>
<p id="Par33">Modulation of Treg differentiation might be a potential therapeutic target but also harbors some pitfalls. Engagement of certain surface molecules and activation of subsequent signaling pathways that might drive Tregs into either Th1-like or Th1-suppressing subtypes can dictate the beneficial outcome in settings of infection or tumor development. Several clinical studies have been undertaken to exploit antibody therapy against CTLA-4 and PD-1/PD-L1 thus dampening intratumoral Treg responses and enabling tumor clearance by effector T cells [<xref ref-type="bibr" rid="CR189">189</xref>
, <xref ref-type="bibr" rid="CR190">190</xref>
]. However, systemic administration of antibodies or other reagents that interfere with Treg signaling pathways harbor the danger of shifting the subpopulation balance in disfavor when considering the performance of other immune responses.</p>
<p id="Par34">Furthermore, the underlying pathways that drive Treg plasticity into either direction seem to be critically dependent on the microenvironment. MS patients display an increased number of IFNγ<sup>+</sup>
Th1-like Tregs that lost suppressive function in peripheral blood and are thus believed to be a crucial factor as to why autoimmune reactions in these patients are not controlled efficiently. The PI3K/AKT/FOXO1/3 pathway has been identified as one of the key pathways involved in Th1-like Treg generation and is an interesting prospective target for immunomodulation [<xref ref-type="bibr" rid="CR153">153</xref>
]. However, IFNγ<sup>+</sup>
Th1-like Tregs in other disease settings do not lose their suppressive function which might indicate the involvement of different signaling pathways ultimately resulting in similar but yet different phenotypic outcomes.</p>
<p id="Par35">Clinically, Tregs have recently been beneficially used for therapy against graft versus host disease following allogeneic bone marrow or stem cell transplantation [<xref ref-type="bibr" rid="CR191">191</xref>
, <xref ref-type="bibr" rid="CR192">192</xref>
] and type 1 diabetes patients [<xref ref-type="bibr" rid="CR193">193</xref>
]. In these settings, autologous polyclonal Tregs are expanded in vitro and re-transferred into the patient. The use of in vitro Treg expansion protocols gives the opportunity to analyze Treg phenotype and function as well as specifically control cell numbers necessary to re-transfer for a beneficial outcome. Several clinical trial studies have reported successful application of Treg transfer therapy in T1D and GVHD [<xref ref-type="bibr" rid="CR193">193</xref>
, <xref ref-type="bibr" rid="CR194">194</xref>
]. As antigen-specific Tregs are more efficient at regulating disease-specific immunological processes, the generation of antigen-specific Tregs using chimeric antigen receptors (CAR) has been explored as well, as an improvement to Treg therapy. CAR Tregs have been shown to prevent GVHD in a humanized mouse model highlighting their improved therapeutic potential [<xref ref-type="bibr" rid="CR195">195</xref>
].</p>
<p id="Par36">Combination of adoptive transfer of antigen-specific Tregs with modulation of Treg plasticity proposes strong therapeutic potential. In vitro expansion of Tregs provides the opportunity to also include cytokine treatments to reprogram Tregs into phenotypic subtypes most beneficial for the respective disease. Furthermore, defective Treg phenotypes could be corrected by either interfering with involved pathways by using pharmacological agents or by introducing recent gene editing technologies such as the CRISPR/Cas9 system.</p>
</sec>
<sec id="Sec12"><title>Conclusions and future perspectives</title>
<p id="Par37">During the past few years it has become clear that Tregs possess some degree of plasticity and can adapt their phenotype to the microenvironment where they exert their functions. Furthermore, aberrant reprogramming of Tregs into Th1-like Tregs has been observed in several human autoimmune diseases, suggesting their contribution to disease. The relative importance of Th1-like Tregs in the pathophysiology of the diseases where they have been observed, their role in promoting or protecting from inflammation-derived damage and their influence in disease outcome are fundamental open questions that remain to be answered and that will undoubtedly provide valuable information for the potential manipulation of Treg plasticity with therapeutic purposes for these diseases. In order to design better therapeutic options targeted to Tregs in cancer, infectious and autoimmune diseases, it is imperative to understand the signaling pathways that govern the acquisition of specific effector characteristics by Tregs in different disease settings. In this regard, most of the current literature on Th1-like Tregs defines IFNγ and IL-12 as the major inducers of Th1- reprogramming in Treg cells. However, the discovery of the PI3K/AKT axis as a major signaling pathway that regulates Th1-like Treg generation, and the variety of upstream ligands/receptors that can activate it, makes the generation of Th1-like Tregs a plausible event in many disease settings, and it strongly suggests that there are likely other environmental cues apart from Th1 cytokines that induce the generation of dysfunctional Th1-Tregs or Th1-suppressing Tregs. Moreover, there are likely many other signaling pathways involved in Th1-like Treg generation in specific disease settings yet to be defined [<xref ref-type="bibr" rid="CR93">93</xref>
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<p id="Par38">In conclusion, it is crucial to fully understand the underlying pathways and mechanisms that regulate Treg plasticity and the environmental cues that induce such phenotypes in specific disease settings in order to be able to take advantage of Treg plasticity for therapeutic purposes. Furthermore, it will be important to perform investigations that focus on understanding the differences between Th1-suppressive Th1-Tregs and dysfunctional Th1-Tregs observed in autoimmune disease settings and acute phases of infection as well as how to transition from one state to another, with potential important applications in therapy.</p>
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