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Intracellular Pathogens: Host Immunity and Microbial Persistence Strategies

Identifieur interne : 000660 ( Pmc/Checkpoint ); précédent : 000659; suivant : 000661

Intracellular Pathogens: Host Immunity and Microbial Persistence Strategies

Auteurs : Aneesh Thakur [Danemark] ; Heidi Mikkelsen [Danemark] ; Gregers Jungersen [Danemark]

Source :

RBID : PMC:6487120

Abstract

Infectious diseases caused by pathogens including viruses, bacteria, fungi, and parasites are ranked as the second leading cause of death worldwide by the World Health Organization. Despite tremendous improvements in global public health since 1950, a number of challenges remain to either prevent or eradicate infectious diseases. Many pathogens can cause acute infections that are effectively cleared by the host immunity, but a subcategory of these pathogens called “intracellular pathogens” can establish persistent and sometimes lifelong infections. Several of these intracellular pathogens manage to evade the host immune monitoring and cause disease by replicating inside the host cells. These pathogens have evolved diverse immune escape strategies and overcome immune responses by residing and multiplying inside host immune cells, primarily macrophages. While these intracellular pathogens that cause persistent infections are phylogenetically diverse and engage in diverse immune evasion and persistence strategies, they share common pathogen type-specific mechanisms during host-pathogen interaction inside host cells. Likewise, the host immune system is also equipped with a diverse range of effector functions to fight against the establishment of pathogen persistence and subsequent host damage. This article provides an overview of the immune effector functions used by the host to counter pathogens and various persistence strategies used by intracellular pathogens to counter host immunity, which enables their extended period of colonization in the host. The improved understanding of persistent intracellular pathogen-derived infections will contribute to develop improved disease diagnostics, therapeutics, and prophylactics.


Url:
DOI: 10.1155/2019/1356540
PubMed: 31111075
PubMed Central: 6487120


Affiliations:


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PMC:6487120

Le document en format XML

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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">J Immunol Res</journal-id>
<journal-id journal-id-type="iso-abbrev">J Immunol Res</journal-id>
<journal-id journal-id-type="publisher-id">JIR</journal-id>
<journal-title-group>
<journal-title>Journal of Immunology Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">2314-8861</issn>
<issn pub-type="epub">2314-7156</issn>
<publisher>
<publisher-name>Hindawi</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">31111075</article-id>
<article-id pub-id-type="pmc">6487120</article-id>
<article-id pub-id-type="doi">10.1155/2019/1356540</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Intracellular Pathogens: Host Immunity and Microbial Persistence Strategies</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0003-0693-6101</contrib-id>
<name>
<surname>Thakur</surname>
<given-names>Aneesh</given-names>
</name>
<email>aneesh.thakur@sund.ku.dk</email>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mikkelsen</surname>
<given-names>Heidi</given-names>
</name>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0003-3147-6960</contrib-id>
<name>
<surname>Jungersen</surname>
<given-names>Gregers</given-names>
</name>
<email>grju@dtu.dk</email>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="I3">
<sup>3</sup>
</xref>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>
Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen Ø, Denmark</aff>
<aff id="I2">
<sup>2</sup>
Section for Immunology and Vaccinology, National Veterinary Institute, Technical University of Denmark, Kemitorvet, 2800 Kgs. Lyngby, Denmark</aff>
<aff id="I3">
<sup>3</sup>
Section for Protein Science and Biotherapeutics, Department of Biotechnology and Biomedicine, Technical University of Denmark, Kemitorvet, 2800 Kgs. Lyngby, Denmark</aff>
<author-notes>
<fn fn-type="other">
<p>Academic Editor: Martin Holland</p>
</fn>
</author-notes>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>14</day>
<month>4</month>
<year>2019</year>
</pub-date>
<volume>2019</volume>
<elocation-id>1356540</elocation-id>
<history>
<date date-type="received">
<day>28</day>
<month>11</month>
<year>2018</year>
</date>
<date date-type="rev-recd">
<day>15</day>
<month>3</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>2</day>
<month>4</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2019 Aneesh Thakur et al.</copyright-statement>
<copyright-year>2019</copyright-year>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>Infectious diseases caused by pathogens including viruses, bacteria, fungi, and parasites are ranked as the second leading cause of death worldwide by the World Health Organization. Despite tremendous improvements in global public health since 1950, a number of challenges remain to either prevent or eradicate infectious diseases. Many pathogens can cause acute infections that are effectively cleared by the host immunity, but a subcategory of these pathogens called “intracellular pathogens” can establish persistent and sometimes lifelong infections. Several of these intracellular pathogens manage to evade the host immune monitoring and cause disease by replicating inside the host cells. These pathogens have evolved diverse immune escape strategies and overcome immune responses by residing and multiplying inside host immune cells, primarily macrophages. While these intracellular pathogens that cause persistent infections are phylogenetically diverse and engage in diverse immune evasion and persistence strategies, they share common pathogen type-specific mechanisms during host-pathogen interaction inside host cells. Likewise, the host immune system is also equipped with a diverse range of effector functions to fight against the establishment of pathogen persistence and subsequent host damage. This article provides an overview of the immune effector functions used by the host to counter pathogens and various persistence strategies used by intracellular pathogens to counter host immunity, which enables their extended period of colonization in the host. The improved understanding of persistent intracellular pathogen-derived infections will contribute to develop improved disease diagnostics, therapeutics, and prophylactics.</p>
</abstract>
<funding-group>
<award-group>
<funding-source>Danish Research Council for Technology and Production Sciences</funding-source>
<award-id>368 274-08-0166</award-id>
</award-group>
</funding-group>
</article-meta>
</front>
<floats-group>
<fig id="fig1" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>Schematic representation of the host immune response against microbial pathogens. Microbial pathogens or antigens can be taken up by the antigen-presenting cells, mostly dendritic cells (DCs), once they breach the epithelial barrier. Antigens are presented to the naive T cells by the activated DCs through major histocompatibility complex–T cell receptor interaction, which leads to activation and expansion of antigen-specific effector T cells (Teff). Teff differentiate into one of the different subtypes, e.g., helper T cells (Th)1, Th2, follicular helper T cells (Tfh), Th17, or regulatory T cells (Tregs), depending on the cytokine milieu of the microenvironment. Th1 cells activate macrophages or CD8
<sup>+</sup>
T cells through production of IFN-
<italic>γ</italic>
. Activated macrophages fuse their lysosomes more efficiently to phagosomes, exposing intracellular microbes to a variety of microbicidal lysosomal enzymes and toxic oxygen and nitrogen metabolites. Cytotoxic T cells (CTL) destroy pathogens through release of perforins and granzymes or induce apoptosis of infected cells. Th2 and Tfh cells activate B cells through production of cytokines and induce the differentiation of B cells into plasma cells, antibody class switching, and affinity maturation of antibodies, which remove the pathogen by neutralization, opsonization, and phagocytosis. Th17 cells participate in neutrophil activation and immune regulation by producing cytokine IL-17A, which is required for protection against extracellular and some intracellular pathogens. Tregs regulate immune responses to pathogens and maintain self-tolerance by negatively regulating Th1 and Th2 cells, e.g., by producing cytokines IL-10 and TGF-
<italic>β</italic>
. Innate immune cells such as eosinophils, basophils, and mast cells play an important role in protection against parasitic infections including helminth infections. Natural killer (NK) and natural killer T (NKT) cells, which form a bridge between innate and adaptive immunity, also contribute to antibacterial and antiviral immunity. NK cells have similar functions as the CTL while NKT cells produce cytokines to execute their killing functions.</p>
</caption>
<graphic xlink:href="JIR2019-1356540.001"></graphic>
</fig>
<fig id="fig2" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>Schematic representation of the mechanisms of persistence of selected intracellular pathogens. Left: an overview of the various mechanisms used by pathogens to overcome innate and adaptive immune responses. The major strategies are discussed in more detail in the text. Right: evasion strategies of various phagocytic mechanisms by selected intracellular pathogens. Viruses such as influenza virus are able to inhibit the activation of antiviral mechanisms, such as the production of interferon upon viral infection, and enter the nucleus.
<italic>Mycobacterium tuberculosis</italic>
after phagocytosis acquires the early endosome marker Rab5, which blocks fusion with the lysosome, and the mycobacteria replicate in this early endosome.
<italic>Legionella pneumophila</italic>
resides and multiplies in vacuoles that acquire Rab1 and secretes effector molecules
<italic>via</italic>
its type IV secretion system, which inhibits phagolysosome formation.
<italic>Listeria monocytogenes</italic>
-engulfed phagosome undergoes acidification, which perforates the phagosomal membrane and the bacteria escape into the cytosol, where they move within and then among cells with actin polymerization.
<italic>Chlamydia</italic>
spp. are present as nonreplicating infectious “elementary body” and intracytoplasmic replicating noninfectious “reticulate body.” The elementary body induces its own endocytosis upon exposure to host cells and survives and multiplies inside phagolysosome before infecting the new host.
<italic>Coxiella burnetii</italic>
and
<italic>Brucella abortus</italic>
are present inside a vacuole, which becomes acidic and acquires Rab5 followed by Rab7 that prevents phagolysosome formation. The
<italic>Francisella tularensis</italic>
phagosome acquires Rab5 (early endosome) and then Rab7 (late endosome). Late endosome is not acidified, which disrupts the phagosomal membrane discharging the bacteria into the cytosol. These vacuoles fuse with the endoplasmic reticulum, which allow bacterial replication.
<italic>Leishmania</italic>
spp. phagosome becomes acidic phagolysosome, which bears Rab7, and the parasite survives and multiplies inside the phagolysosome.</p>
</caption>
<graphic xlink:href="JIR2019-1356540.002"></graphic>
</fig>
<table-wrap id="tab1" orientation="portrait" position="float">
<label>Table 1</label>
<caption>
<p>Lymphocyte subsets in the control of microbial infections.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Lymphocyte subset</th>
<th align="center" rowspan="1" colspan="1">Antigen presentation</th>
<th align="center" rowspan="1" colspan="1">Transcription factors</th>
<th align="center" rowspan="1" colspan="1">Effector molecules secreted</th>
<th align="center" rowspan="1" colspan="1">Mechanism</th>
<th align="center" rowspan="1" colspan="1">Evidence for control in intracellular infections (gene deficiency or direct involvement)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="4" colspan="1">Th1</td>
<td align="center" rowspan="4" colspan="1">MHC class II</td>
<td align="center" rowspan="4" colspan="1">T-bet, STAT4, STAT1</td>
<td align="center" rowspan="4" colspan="1">IFN-
<italic>γ</italic>
, TNF-
<italic>α</italic>
, IL-2, lymphotoxin
<italic>α</italic>
</td>
<td align="center" rowspan="4" colspan="1">Activation of macrophages by IFN-
<italic>γ</italic>
, upregulation of iNOS and ROI, proliferation of CTL</td>
<td align="center" rowspan="1" colspan="1">IFN-
<italic>γ</italic>
-/- [
<xref rid="B16" ref-type="bibr">16</xref>
<xref rid="B21" ref-type="bibr">21</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">TNF-
<italic>α</italic>
-/- [
<xref rid="B22" ref-type="bibr">22</xref>
<xref rid="B29" ref-type="bibr">29</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-12p40 -/- [
<xref rid="B30" ref-type="bibr">30</xref>
<xref rid="B32" ref-type="bibr">32</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-18 -/- [
<xref rid="B33" ref-type="bibr">33</xref>
<xref rid="B35" ref-type="bibr">35</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Th2</td>
<td align="center" rowspan="1" colspan="1">MHC class II</td>
<td align="center" rowspan="1" colspan="1">GATA3, STAT5, STAT6</td>
<td align="center" rowspan="1" colspan="1">IL-4, IL-5, IL-9, IL-13</td>
<td align="center" rowspan="1" colspan="1">Stimulate B cells, antibody production, antibody class switching</td>
<td align="center" rowspan="1" colspan="1">Th2 cytokines [
<xref rid="B30" ref-type="bibr">30</xref>
<xref rid="B32" ref-type="bibr">32</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="4" colspan="1">Th17</td>
<td align="center" rowspan="4" colspan="1">MHC class II</td>
<td align="center" rowspan="4" colspan="1">ROR
<italic>γ</italic>
t, STAT3</td>
<td align="center" rowspan="4" colspan="1">IL-17A, IL-17F, IL-21, IL-22, CCL20</td>
<td align="center" rowspan="4" colspan="1">Recruitment, activation and migration of neutrophils</td>
<td align="center" rowspan="1" colspan="1">IL-17 -/- [
<xref rid="B36" ref-type="bibr">36</xref>
<xref rid="B41" ref-type="bibr">41</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-17 RA -/- [
<xref rid="B42" ref-type="bibr">42</xref>
<xref rid="B47" ref-type="bibr">47</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IFN-
<italic>γ</italic>
-/- [
<xref rid="B16" ref-type="bibr">16</xref>
,
<xref rid="B18" ref-type="bibr">18</xref>
,
<xref rid="B19" ref-type="bibr">19</xref>
,
<xref rid="B48" ref-type="bibr">48</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-23 -/- [
<xref rid="B31" ref-type="bibr">31</xref>
,
<xref rid="B49" ref-type="bibr">49</xref>
<xref rid="B51" ref-type="bibr">51</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="3" colspan="1">Tfh</td>
<td align="center" rowspan="3" colspan="1">MHC class II</td>
<td align="center" rowspan="3" colspan="1">Bcl6, c-MAF</td>
<td align="center" rowspan="3" colspan="1">IL-10, IL-21</td>
<td align="center" rowspan="3" colspan="1">Provides help for B cells to allow formation of plasma cells and memory B cells</td>
<td align="center" rowspan="1" colspan="1">Tfh -/- [
<xref rid="B52" ref-type="bibr">52</xref>
,
<xref rid="B53" ref-type="bibr">53</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-21 -/- [
<xref rid="B54" ref-type="bibr">54</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-6 -/- [
<xref rid="B55" ref-type="bibr">55</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="4" colspan="1">Tregs</td>
<td align="center" rowspan="4" colspan="1">MHC class II</td>
<td align="center" rowspan="4" colspan="1">FOXP3, SMAD, STAT5</td>
<td align="center" rowspan="4" colspan="1">IL-10, TGF-
<italic>β</italic>
, IL-35</td>
<td align="center" rowspan="4" colspan="1">Immunosuppression and tolerance</td>
<td align="center" rowspan="1" colspan="1">CD4
<sup>+</sup>
Tregs [
<xref rid="B56" ref-type="bibr">56</xref>
<xref rid="B58" ref-type="bibr">58</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">CD8
<sup>+</sup>
Tregs [
<xref rid="B59" ref-type="bibr">59</xref>
<xref rid="B61" ref-type="bibr">61</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-10 -/- [
<xref rid="B57" ref-type="bibr">57</xref>
,
<xref rid="B62" ref-type="bibr">62</xref>
,
<xref rid="B63" ref-type="bibr">63</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">TGF-
<italic>β</italic>
-/- [
<xref rid="B64" ref-type="bibr">64</xref>
,
<xref rid="B65" ref-type="bibr">65</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="4" colspan="1">CD8
<sup>+</sup>
/CTL</td>
<td align="center" rowspan="4" colspan="1">MHC class I</td>
<td align="center" rowspan="4" colspan="1">EOMES, BLIMP1</td>
<td align="center" rowspan="4" colspan="1">IFN-
<italic>γ</italic>
, perforin, granzyme, granulysin, FAS-FAS ligand</td>
<td align="center" rowspan="4" colspan="1">Cytotoxicity, programmed cell death by caspase or receptor-mediated FAS-FAS ligand apoptosis</td>
<td align="center" rowspan="1" colspan="1">IFN-
<italic>γ</italic>
-/- [
<xref rid="B66" ref-type="bibr">66</xref>
<xref rid="B71" ref-type="bibr">71</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">TNF-
<italic>α</italic>
-/- [
<xref rid="B22" ref-type="bibr">22</xref>
<xref rid="B28" ref-type="bibr">28</xref>
,
<xref rid="B72" ref-type="bibr">72</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Perforin -/- [
<xref rid="B73" ref-type="bibr">73</xref>
<xref rid="B75" ref-type="bibr">75</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Granzyme -/- [
<xref rid="B75" ref-type="bibr">75</xref>
,
<xref rid="B76" ref-type="bibr">76</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="3" colspan="1">
<italic>γδ</italic>
T</td>
<td align="center" rowspan="3" colspan="1">CD1c</td>
<td align="center" rowspan="3" colspan="1">PLZF, GATA3, TBX21</td>
<td align="center" rowspan="3" colspan="1">IFN-
<italic>γ</italic>
, IL-17A, IL-17F, IL-22</td>
<td align="center" rowspan="3" colspan="1">Pro- and anti-inflammatory functions at epithelial surfaces</td>
<td align="center" rowspan="1" colspan="1">
<italic>γδ</italic>
TCR -/- [
<xref rid="B77" ref-type="bibr">77</xref>
<xref rid="B82" ref-type="bibr">82</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-17 [
<xref rid="B37" ref-type="bibr">37</xref>
,
<xref rid="B38" ref-type="bibr">38</xref>
,
<xref rid="B46" ref-type="bibr">46</xref>
,
<xref rid="B83" ref-type="bibr">83</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IL-22 [
<xref rid="B84" ref-type="bibr">84</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="3" colspan="1">NK</td>
<td align="center" rowspan="3" colspan="1">MHC class I are inhibitory</td>
<td align="center" rowspan="3" colspan="1">PU.1, Ets-1, GATA3, IRF-2</td>
<td align="center" rowspan="3" colspan="1">IFN-
<italic>γ</italic>
, TNF-
<italic>α</italic>
, perforin, granzyme,
<italic>α</italic>
-defensins</td>
<td align="center" rowspan="3" colspan="1">Cytotoxic, direct cytolysis by apoptosis, ADCC</td>
<td align="center" rowspan="1" colspan="1">NK -/- [
<xref rid="B85" ref-type="bibr">85</xref>
,
<xref rid="B86" ref-type="bibr">86</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">IFN-
<italic>γ</italic>
-/- [
<xref rid="B87" ref-type="bibr">87</xref>
,
<xref rid="B88" ref-type="bibr">88</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Perforin -/- [
<xref rid="B87" ref-type="bibr">87</xref>
,
<xref rid="B89" ref-type="bibr">89</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">iNKT</td>
<td align="center" rowspan="1" colspan="1">CD1d</td>
<td align="center" rowspan="1" colspan="1">PLZF, TBX21, ERK</td>
<td align="center" rowspan="1" colspan="1">IL-4, IFN-
<italic>γ</italic>
, IL-17A, GM-CSF</td>
<td align="center" rowspan="1" colspan="1">Pro- and anti-inflammatory functions</td>
<td align="center" rowspan="1" colspan="1">iNKT cells [
<xref rid="B90" ref-type="bibr">90</xref>
<xref rid="B95" ref-type="bibr">95</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="2" colspan="1">MAIT</td>
<td align="center" rowspan="2" colspan="1">MR1</td>
<td align="center" rowspan="2" colspan="1">ZBTB16, ROR(
<italic>γ</italic>
t)</td>
<td align="center" rowspan="2" colspan="1">IFN-
<italic>γ</italic>
, TNF-
<italic>α</italic>
, IL-17, granzyme</td>
<td align="center" rowspan="2" colspan="1">Cytokine production, cytotoxic</td>
<td align="center" rowspan="1" colspan="1">MAIT -/- [
<xref rid="B96" ref-type="bibr">96</xref>
<xref rid="B98" ref-type="bibr">98</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">MR -/- [
<xref rid="B99" ref-type="bibr">99</xref>
<xref rid="B101" ref-type="bibr">101</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="6" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="2" colspan="1">B</td>
<td align="center" rowspan="2" colspan="1">NA</td>
<td align="center" rowspan="2" colspan="1">PU.1, Pax5 Ikaros</td>
<td align="center" rowspan="2" colspan="1">Immunoglobulins, IL-10</td>
<td align="center" rowspan="2" colspan="1">Antibody secretion, neutralization, opsonization, phagocytosis, antigen presentation</td>
<td align="center" rowspan="1" colspan="1">B cells [
<xref rid="B102" ref-type="bibr">102</xref>
<xref rid="B108" ref-type="bibr">108</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Polymeric-Ig receptor -/- [
<xref rid="B109" ref-type="bibr">109</xref>
<xref rid="B113" ref-type="bibr">113</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>ADCC: antibody-dependent cellular cytotoxicity; B: B lymphocyte; Bcl6: B cell lymphoma 6; BLIMP1: PR domain zinc finger protein 1; CCL: chemokine ligand; CD: cluster of differentiation; c-MAF: c-musculoaponeurotic fibrosarcoma oncogene homolog; CTL: cytotoxic T lymphocyte; EOMES: Eomesodermin; ERK: extracellular signal-regulated kinase; Ets-1: erythroblastosis virus transcription factor-1; FOXP3: Forkhead box P3; GATA, trans-acting T cell-specific transcription factor;
<italic>γδ</italic>
T: gamma delta T cells; GM-CSF: granulocyte-macrophage colony-stimulating factor; IFN-
<italic>γ</italic>
: interferon gamma; Ig: immunoglobulin; IL: interleukin; IL-17RA: interleukin 17 receptor a; iNKT: invariant natural killer T cell; iNOS: inducible nitric oxide synthase; IRF-2: interferon regulatory factor 2; MHC: major histocompatibility complex; MR1: major histocompatibility complex class I-related gene protein; MAIT: mucosal-associated invariant T cells; NA: not applicable; NK: natural killer cells; Pax5: paired box protein 5; PLZF: promyelocytic leukemia zinc finger; ROR
<italic>γ</italic>
t: RAR-related orphan receptor gamma 2; ROI: reactive oxygen intermediates; STAT: signal transducer and activator of transcription; TBX: T-box transcription factor; Tfh: follicular helper T cells; TGF-
<italic>β</italic>
: transforming growth factor beta; Th: helper T cells; TNF-
<italic>α</italic>
: tumor necrosis factor alpha; Tregs: regulatory T cells; ZBTB16: zinc finger and BTB domain-containing protein 16.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tab2" orientation="portrait" position="float">
<label>Table 2</label>
<caption>
<p>Selected mechanisms for evasion of host defense by persistent intracellular pathogens.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Mechanism</th>
<th align="center" rowspan="1" colspan="1">Pathogen(s)</th>
<th align="center" rowspan="1" colspan="1">Pathogen type</th>
<th align="center" rowspan="1" colspan="1">Remarks</th>
<th align="center" rowspan="1" colspan="1">Reference(s)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="9" colspan="1">Immunomodulation</td>
<td align="center" rowspan="1" colspan="1">
<italic>Salmonella</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Lipid A modification</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B186" ref-type="bibr">186</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Leptospira interrogans</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Peptidoglycan modification</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B187" ref-type="bibr">187</xref>
,
<xref rid="B188" ref-type="bibr">188</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Poxvirus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Host cytokine decoy receptors</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B189" ref-type="bibr">189</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Herpesvirus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Host cytokine and chemokine decoy receptors</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B190" ref-type="bibr">190</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Mycobacterium tuberculosis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">ESX secretion system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B191" ref-type="bibr">191</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Salmonella typhimurium</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Type III secretion system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B192" ref-type="bibr">192</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Brucella abortus</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Type IV secretion system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B193" ref-type="bibr">193</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Staphylococcus aureus</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Ess secretion system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B194" ref-type="bibr">194</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Bacillus subtilis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Yuk/Yue secretion system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B195" ref-type="bibr">195</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="5" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="7" colspan="1">Antigenic variation</td>
<td align="center" rowspan="1" colspan="1">Influenza virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Antigenic drift/shift</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B196" ref-type="bibr">196</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Neisseria</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">DNA rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B197" ref-type="bibr">197</xref>
,
<xref rid="B198" ref-type="bibr">198</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Plasmodium</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Programmed gene rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B199" ref-type="bibr">199</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>S. Typhimurium</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">DNA rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B200" ref-type="bibr">200</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Trypanosoma brucei</italic>
</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Programmed gene rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B201" ref-type="bibr">201</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Hepatitis C virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">DNA rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B202" ref-type="bibr">202</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Human immunodeficiency virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">DNA rearrangement</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B203" ref-type="bibr">203</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="5" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="7" colspan="1">Hiding in safe target cells/tissues</td>
<td align="center" rowspan="1" colspan="1">Epstein-Barr virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">B cells</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B204" ref-type="bibr">204</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Herpes simplex virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Sensory neurons</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B27" ref-type="bibr">27</xref>
,
<xref rid="B205" ref-type="bibr">205</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Leishmania</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Fibroblasts</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B206" ref-type="bibr">206</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Mycobacterium leprae</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Peripheral nerves (Schwann cells)</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B207" ref-type="bibr">207</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Salmonella enterica</italic>
Typhi</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Reticuloendothelial system</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B208" ref-type="bibr">208</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Toxoplasma</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Cerebellar neurons</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B209" ref-type="bibr">209</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Varicella zoster virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Dorsal root ganglia</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B210" ref-type="bibr">210</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>B: bacteria; P: protozoa; V: virus.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<table-wrap id="tab3" orientation="portrait" position="float">
<label>Table 3</label>
<caption>
<p>Selected mechanisms for modulation/suppression of host immune response by persistent intracellular pathogens.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Mechanism</th>
<th align="center" rowspan="1" colspan="1">Pathogen(s)</th>
<th align="center" rowspan="1" colspan="1">Pathogen type</th>
<th align="center" rowspan="1" colspan="1">Remarks</th>
<th align="center" rowspan="1" colspan="1">Reference(s)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="10" colspan="1">Subversion of host defense</td>
<td align="center" rowspan="1" colspan="1">
<italic>Brucella</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Inhibit fusion with host lysosomal compartment and alter lysosomal pH</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B211" ref-type="bibr">211</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Chlamydiae</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Degradation of host proteins and deactivation of neutrophils by chlamydial protease-like activating factor</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B212" ref-type="bibr">212</xref>
,
<xref rid="B213" ref-type="bibr">213</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Francisella tularensis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Escape into cytosol</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B214" ref-type="bibr">214</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Anaplasma phagocytophilum</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Inhibits autophagosomal-lysosomal fusion</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B215" ref-type="bibr">215</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Legionella pneumophila</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Membrane-bound vacuole and effector protein (Ank protein) release</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B216" ref-type="bibr">216</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Listeria monocytogenes</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Escape into cytosol</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B217" ref-type="bibr">217</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Mycobacterium tuberculosis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Inhibition of phagolysosome formation</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B183" ref-type="bibr">183</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Rickettsia</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Escape into cytosol and replicate in cytoplasm of host cell</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B218" ref-type="bibr">218</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Salmonella enterica</italic>
Typhi</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Inhibit fusion with host lysosomal compartment and alter lysosomal pH</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B36" ref-type="bibr">36</xref>
,
<xref rid="B219" ref-type="bibr">219</xref>
,
<xref rid="B220" ref-type="bibr">220</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Toxoplasma gondii</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Generate own vesicle</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B221" ref-type="bibr">221</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="5" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="6" colspan="1">Resistance to host effector mechanisms</td>
<td align="center" rowspan="1" colspan="1">Cytomegalovirus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Inhibition of humoral immunity and inflammatory response. Blockage of Ag processing and presentation</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B63" ref-type="bibr">63</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Epstein-Barr virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Inhibition of inflammatory response</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B204" ref-type="bibr">204</xref>
,
<xref rid="B222" ref-type="bibr">222</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Herpes simplex virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Inhibition of humoral immunity and blockage of Ag processing and presentation</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B27" ref-type="bibr">27</xref>
,
<xref rid="B205" ref-type="bibr">205</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Leishmania</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Silent phagocytosis</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B206" ref-type="bibr">206</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Mycobacterium tuberculosis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Ability to persist in macrophages</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B183" ref-type="bibr">183</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Vaccinia virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Inhibition of humoral immunity and inflammatory response</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B223" ref-type="bibr">223</xref>
<xref rid="B225" ref-type="bibr">225</xref>
]</td>
</tr>
<tr>
<td align="center" colspan="5" rowspan="1">
<hr></hr>
</td>
</tr>
<tr>
<td align="left" rowspan="7" colspan="1">Induction of inappropriate immune responses/immunosuppression/Tregs</td>
<td align="center" rowspan="1" colspan="1">Hepatitis C virus (HCV)</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Immunosuppression by complement regulatory pathway</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B160" ref-type="bibr">160</xref>
,
<xref rid="B226" ref-type="bibr">226</xref>
<xref rid="B228" ref-type="bibr">228</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Mycobacterium leprae</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Immunosuppression of Th2 cytokines, indoleamine 2, 3-dioxygenase</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B159" ref-type="bibr">159</xref>
,
<xref rid="B229" ref-type="bibr">229</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">HCV</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Induction of Tregs</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B160" ref-type="bibr">160</xref>
,
<xref rid="B227" ref-type="bibr">227</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">Human immunodeficiency virus</td>
<td align="center" rowspan="1" colspan="1">V</td>
<td align="center" rowspan="1" colspan="1">Induction of Tregs</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B161" ref-type="bibr">161</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Leishmania major</italic>
</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Induction of Tregs</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B103" ref-type="bibr">103</xref>
,
<xref rid="B230" ref-type="bibr">230</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>M. Tuberculosis</italic>
</td>
<td align="center" rowspan="1" colspan="1">B</td>
<td align="center" rowspan="1" colspan="1">Induction of Tregs</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B231" ref-type="bibr">231</xref>
]</td>
</tr>
<tr>
<td align="center" rowspan="1" colspan="1">
<italic>Plasmodium</italic>
spp.</td>
<td align="center" rowspan="1" colspan="1">P</td>
<td align="center" rowspan="1" colspan="1">Induction of Tregs</td>
<td align="center" rowspan="1" colspan="1">[
<xref rid="B232" ref-type="bibr">232</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Ag: antigen; B: bacteria; P: protozoa; Th2: type 2 helper T cells; Tregs: regulatory T cells; V: virus.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</floats-group>
</pmc>
<affiliations>
<list>
<country>
<li>Danemark</li>
</country>
</list>
<tree>
<country name="Danemark">
<noRegion>
<name sortKey="Thakur, Aneesh" sort="Thakur, Aneesh" uniqKey="Thakur A" first="Aneesh" last="Thakur">Aneesh Thakur</name>
</noRegion>
<name sortKey="Jungersen, Gregers" sort="Jungersen, Gregers" uniqKey="Jungersen G" first="Gregers" last="Jungersen">Gregers Jungersen</name>
<name sortKey="Jungersen, Gregers" sort="Jungersen, Gregers" uniqKey="Jungersen G" first="Gregers" last="Jungersen">Gregers Jungersen</name>
<name sortKey="Mikkelsen, Heidi" sort="Mikkelsen, Heidi" uniqKey="Mikkelsen H" first="Heidi" last="Mikkelsen">Heidi Mikkelsen</name>
</country>
</tree>
</affiliations>
</record>

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