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Methotrexate an Old Drug with New Tricks

Identifieur interne : 000A23 ( Pmc/Curation ); précédent : 000A22; suivant : 000A24

Methotrexate an Old Drug with New Tricks

Auteurs : Yosra Bedoui ; Xavier Guillot ; Jimmy Sélambarom ; Pascale Guiraud ; Claude Giry ; Marie Christine Jaffar-Bandjee ; Stéphane Ralandison ; Philippe Gasque [France]

Source :

RBID : PMC:6834162

Abstract

Methotrexate (MTX) is the first line drug for the treatment of a number of rheumatic and non-rheumatic disorders. It is currently used as an anchor disease, modifying anti-rheumatic drug in the treatment of rheumatoid arthritis (RA). Despite the development of numerous new targeted therapies, MTX remains the backbone of RA therapy due to its potent efficacy and tolerability. There has been also a growing interest in the use of MTX in the treatment of chronic viral mediated arthritis. Many viruses—including old world alphaviruses, Parvovirus B19, hepatitis B/C virus, and human immunodeficiency virus—have been associated with arthritogenic diseases and reminiscent of RA. MTX may provide benefits although with the potential risk of attenuating patients’ immune surveillance capacities. In this review, we describe the emerging mechanisms of action of MTX as an anti-inflammatory drug and complementing its well-established immunomodulatory activity. The mechanisms involve adenosine signaling modulation, alteration of cytokine networks, generation of reactive oxygen species and HMGB1 alarmin suppression. We also provide a comprehensive understanding of the mechanisms of MTX toxic effects. Lastly, we discussed the efficacy, as well as the safety, of MTX used in the management of viral-related rheumatic syndromes.


Url:
DOI: 10.3390/ijms20205023
PubMed: 31658782
PubMed Central: 6834162

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PMC:6834162

Le document en format XML

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<p>Methotrexate (MTX) is the first line drug for the treatment of a number of rheumatic and non-rheumatic disorders. It is currently used as an anchor disease, modifying anti-rheumatic drug in the treatment of rheumatoid arthritis (RA). Despite the development of numerous new targeted therapies, MTX remains the backbone of RA therapy due to its potent efficacy and tolerability. There has been also a growing interest in the use of MTX in the treatment of chronic viral mediated arthritis. Many viruses—including old world alphaviruses, Parvovirus B19, hepatitis B/C virus, and human immunodeficiency virus—have been associated with arthritogenic diseases and reminiscent of RA. MTX may provide benefits although with the potential risk of attenuating patients’ immune surveillance capacities. In this review, we describe the emerging mechanisms of action of MTX as an anti-inflammatory drug and complementing its well-established immunomodulatory activity. The mechanisms involve adenosine signaling modulation, alteration of cytokine networks, generation of reactive oxygen species and HMGB1 alarmin suppression. We also provide a comprehensive understanding of the mechanisms of MTX toxic effects. Lastly, we discussed the efficacy, as well as the safety, of MTX used in the management of viral-related rheumatic syndromes.</p>
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<name sortKey="Berger, T G" uniqKey="Berger T">T.G. Berger</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Masson, C" uniqKey="Masson C">C. Masson</name>
</author>
<author>
<name sortKey="Chennebault, J M" uniqKey="Chennebault J">J.M. Chennebault</name>
</author>
<author>
<name sortKey="Leclech, C" uniqKey="Leclech C">C. Leclech</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Int J Mol Sci</journal-id>
<journal-id journal-id-type="iso-abbrev">Int J Mol Sci</journal-id>
<journal-id journal-id-type="publisher-id">ijms</journal-id>
<journal-title-group>
<journal-title>International Journal of Molecular Sciences</journal-title>
</journal-title-group>
<issn pub-type="epub">1422-0067</issn>
<publisher>
<publisher-name>MDPI</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">31658782</article-id>
<article-id pub-id-type="pmc">6834162</article-id>
<article-id pub-id-type="doi">10.3390/ijms20205023</article-id>
<article-id pub-id-type="publisher-id">ijms-20-05023</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Methotrexate an Old Drug with New Tricks</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Bedoui</surname>
<given-names>Yosra</given-names>
</name>
<xref ref-type="aff" rid="af1-ijms-20-05023">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guillot</surname>
<given-names>Xavier</given-names>
</name>
<xref ref-type="aff" rid="af2-ijms-20-05023">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sélambarom</surname>
<given-names>Jimmy</given-names>
</name>
<xref ref-type="aff" rid="af1-ijms-20-05023">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guiraud</surname>
<given-names>Pascale</given-names>
</name>
<xref ref-type="aff" rid="af1-ijms-20-05023">1</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="true">https://orcid.org/0000-0002-4286-0063</contrib-id>
<name>
<surname>Giry</surname>
<given-names>Claude</given-names>
</name>
<xref ref-type="aff" rid="af3-ijms-20-05023">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jaffar-Bandjee</surname>
<given-names>Marie Christine</given-names>
</name>
<xref ref-type="aff" rid="af3-ijms-20-05023">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ralandison</surname>
<given-names>Stéphane</given-names>
</name>
<xref ref-type="aff" rid="af4-ijms-20-05023">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gasque</surname>
<given-names>Philippe</given-names>
</name>
<xref ref-type="aff" rid="af1-ijms-20-05023">1</xref>
<xref ref-type="aff" rid="af5-ijms-20-05023">5</xref>
<xref rid="c1-ijms-20-05023" ref-type="corresp">*</xref>
</contrib>
</contrib-group>
<aff id="af1-ijms-20-05023">
<label>1</label>
Unité Mixte de Recherche Processus Infectieux en Milieu Insulaire Tropical (PIMIT), INSERM U1187, CNRS 9192, IRD 249, Université de La Réunion—Plateforme Technologique CYROI—2, rue Maxime Rivière, 97490 Sainte-Clotilde, France;
<email>yosra.bedoui.bouhouch@gmail.com</email>
(Y.B.);
<email>jimmy.selambarom@univ-reunion.fr</email>
(J.S.);
<email>pascale.guiraud@univ-reunion.fr</email>
(P.G.)</aff>
<aff id="af2-ijms-20-05023">
<label>2</label>
Service de Rhumatologie, CHU La Réunion site Félix Guyon, Allée des Topazes, CS11021, 97400 Saint Denis de La Réunion, France;
<email>xavier.guillot@chu-reunion.fr</email>
</aff>
<aff id="af3-ijms-20-05023">
<label>3</label>
Laboratoire de biologie, CNR associé des arbovirus, CHU La Réunion site Félix Guyon, Allée des Topazes, CS11021, 97400 Saint Denis de La Réunion, France;
<email>claude.giry@chu-reunion.fr</email>
(C.G.);
<email>marie-christine.jaffarbandjee@chu-reunion.fr</email>
(M.C.J.-B.)</aff>
<aff id="af4-ijms-20-05023">
<label>4</label>
Service de Rhumatologie—Médecine Interne, CHU Morafeno, Route d’Ivoloina 501, Toamasina, Madagascar;
<email>stephane_ralandison@yahoo.fr</email>
</aff>
<aff id="af5-ijms-20-05023">
<label>5</label>
Pôle de Biologie, secteur Laboratoire d’Immunologie Clinique et Expérimentale de la zone de l’Océan Indien (LICE-OI), CHU La Réunion site Félix Guyon, Allée des Topazes, CS11021, 97400 Saint Denis de La Réunion, France</aff>
<author-notes>
<corresp id="c1-ijms-20-05023">
<label>*</label>
Correspondence:
<email>philippe.gasque@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>10</day>
<month>10</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<month>10</month>
<year>2019</year>
</pub-date>
<volume>20</volume>
<issue>20</issue>
<elocation-id>5023</elocation-id>
<history>
<date date-type="received">
<day>23</day>
<month>7</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>9</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© 2019 by the authors.</copyright-statement>
<copyright-year>2019</copyright-year>
<license license-type="open-access">
<license-p>Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
).</license-p>
</license>
</permissions>
<abstract>
<p>Methotrexate (MTX) is the first line drug for the treatment of a number of rheumatic and non-rheumatic disorders. It is currently used as an anchor disease, modifying anti-rheumatic drug in the treatment of rheumatoid arthritis (RA). Despite the development of numerous new targeted therapies, MTX remains the backbone of RA therapy due to its potent efficacy and tolerability. There has been also a growing interest in the use of MTX in the treatment of chronic viral mediated arthritis. Many viruses—including old world alphaviruses, Parvovirus B19, hepatitis B/C virus, and human immunodeficiency virus—have been associated with arthritogenic diseases and reminiscent of RA. MTX may provide benefits although with the potential risk of attenuating patients’ immune surveillance capacities. In this review, we describe the emerging mechanisms of action of MTX as an anti-inflammatory drug and complementing its well-established immunomodulatory activity. The mechanisms involve adenosine signaling modulation, alteration of cytokine networks, generation of reactive oxygen species and HMGB1 alarmin suppression. We also provide a comprehensive understanding of the mechanisms of MTX toxic effects. Lastly, we discussed the efficacy, as well as the safety, of MTX used in the management of viral-related rheumatic syndromes.</p>
</abstract>
<kwd-group>
<kwd>methotrexate</kwd>
<kwd>arthritis</kwd>
<kwd>inflammation</kwd>
<kwd>alarmin</kwd>
<kwd>virus</kwd>
<kwd>chikungunya</kwd>
<kwd>rheumatoid arthritis</kwd>
<kwd>innate immunity</kwd>
<kwd>pharmacology</kwd>
</kwd-group>
</article-meta>
</front>
<floats-group>
<fig id="ijms-20-05023-f001" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>Pharmacokinetic process of MTX after oral administration. MTX absorption, distribution, metabolism, and excretion after oral administration.</p>
</caption>
<graphic xlink:href="ijms-20-05023-g001"></graphic>
</fig>
<fig id="ijms-20-05023-f002" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>Methotrexate (MTX) transporters, metabolic pathways and intracellular enzyme targets. MTX transport across biological membranes is mediated by the reduced folate carrier (RFC1), the proton-coupled folate transporter (PCFT) (mainly expressed in the proximal part of the small intestine at the apical membrane of enterocytes) with limited contribution of folate receptors (FR). MTX is exported from the cell by the ATP-binding cassette (ABCC)-family transporters. Within the cell, MTX is converted to polyglutamate forms in a reversible reaction mediated by folylpolyglutamate synthetase (FPGS) and γ-glutamyl hydrolase (GGH). Polyglutamation reduces MTX efflux from the cell via ABCC transporters and therefore increases intracellular half-life of MTX. Intracellular formation of MTX polyglutamate also plays a critical role in MTX activity, increasing inhibition of dihydrofolate reductase (DHFR) and several folate dependent enzymes such as thymidylate synthase (TYMS), 5-amino-imidazole-4-carboxide ribonucleotide (AICAR) transformylase (ATIC), and methylene tetrahydrofolate reductase (MTHFR) decreasing downstream folate pathway intermediates required for nucleotide synthesis. DHF, dihydrofolate; THF, tetrahydrofolate; FAICAR, formyl AICAR; MS, methionine synthetase; dTMP, deoxythymidine monophosphate.</p>
</caption>
<graphic xlink:href="ijms-20-05023-g002"></graphic>
</fig>
<fig id="ijms-20-05023-f003" orientation="portrait" position="float">
<label>Figure 3</label>
<caption>
<p>Immune regulatory action of low dose MTX in the RA synovial tissue. MTX treatment reduces proinflammatory monocytic/macrophagic cytokine (IL1β, IL6, and TNF-α) production, increases Th2 anti-inflammatory cytokine (IL4 and L10) gene expression, and decreases Th1 proinflammatory cytokine (IL2 and IFNγ) gene expression. MTX downregulates IgG Fc receptors FcγRI and IIa expression levels on monocytes decreasing their activation. MTX seems to disrupt synovial fibroblasts and T cells cross-talk signals by inducing inhibition of IL15, IL6, and IL8 expression by synovial fibroblasts, as well as IFNγ and IL17 expression in co-cultured RA T lymphocytes. MTX increases ROS synthesis in T cells, monocytes and neutrophils. MTX reduces T cells and monocytes growth and increases their apoptosis through the generation of ROS. MTX seems to have inhibitory effect on prostaglandin E2 (PGE2) production as well as on the expression of its synthesizing enzymes microsomal prostaglandin E2 synthase 1 (mPGES-1) and cyclooxygenase (COX) 2. MTX reduces synovial metalloproteinase (MMP) production and stimulates their inhibitors (TIMPs).</p>
</caption>
<graphic xlink:href="ijms-20-05023-g003"></graphic>
</fig>
<fig id="ijms-20-05023-f004" orientation="portrait" position="float">
<label>Figure 4</label>
<caption>
<p>MTX affects several signal transduction pathways implicated in the pathogenesis of rheumatoid arthritis (RA). Dysfunctional intracellular signaling involving deregulated activation of the Janus Kinase/Signal Transducers and Activators of Transcription (JAK/STAT) and nuclear factor-κB (NF-κB) activation pathways play a critical role in RA. MTX seems to be a potent suppressor of JAK/STAT signaling pathway which is responsible for the transduction of multiple pro-inflammatory cytokines implicated in the pathogenesis of RA. MTX reduces JAK1, JAK2, STAT1, and STAT5 phosphorylation. Low dose MTX strongly suppresses levels of phosphorylated STAT5. Moreover, MTX-mediated ROS production activates the mitogen-activated protein kinase (MAPK), Jun-N-terminal kinase (JNK), and JNK-dependent induction of p53, which is the final mediator of inhibition of NF-κB activation. NF-κB is involved in inflammation, immune response and cell proliferation and survival. MTX-mediated JNK activation also activates prototypical JNK downstream targets, c-JUN and c-FOS, components of the AP-1 complex which is involved in the increased expression of pro apoptotic genes (such as TNF-α, Fas-L, and Bak) mediating increased sensitivity of cells to apoptosis.</p>
</caption>
<graphic xlink:href="ijms-20-05023-g004"></graphic>
</fig>
<fig id="ijms-20-05023-f005" orientation="portrait" position="float">
<label>Figure 5</label>
<caption>
<p>MTX inhibits HMGB-1/RAGE interaction. HMGB1 released by activated immune cells (macrophages, monocytes, and dendritic cells) or by injured cells acts as an important mediator of inflammation or alarmin. HMGB-1 activates cells through the engagement of multiple surface receptors including TLR2, TLR4, and RAGE. Downstream signaling of HMGB1 is mediated by a number of adaptor proteins, which converge through pathways involving mitogen-activated protein kinase (MAPK) and nuclear factor kappa B (NFκB) and transcriptional regulator, p53 pathways (Weber et al. 2015). HMGB-1 signaling through RAGE promotes maturation of immune cells, chemotaxis and release of pro-inflammatory cytokines (TNF-α, IL-1, IL-6, and IL-8). MTX can bind to the RAGE binding domains of HMGB1 and inhibits the interaction between HMGB1 and its receptor RAGE, thus inhibiting the development of inflammatory responses. Binding of MTX to part of the RAGE-binding region in HMGB1 may be significant for the anti-inflammatory effect of MTX.</p>
</caption>
<graphic xlink:href="ijms-20-05023-g005"></graphic>
</fig>
<table-wrap id="ijms-20-05023-t001" orientation="portrait" position="float">
<object-id pub-id-type="pii">ijms-20-05023-t001_Table 1</object-id>
<label>Table 1</label>
<caption>
<p>Major low dose MTX related adverse events.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Organ System</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">MTX Related Adverse Events</th>
<th align="center" valign="middle" style="border-top:solid thin;border-bottom:solid thin" rowspan="1" colspan="1">Toxic Mechanism of Action</th>
</tr>
</thead>
<tbody>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Gastrointestinal</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Nausea;
<break></break>
Vomiting;
<break></break>
Diarrhea;
<break></break>
Mucositis and stomatitis</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Gastrointestinal toxicities and bone marrow suppression seem to be directly related to folate antagonism, because these tissues have high cell turnover with a high requirement for purines, thymidine, and pyrimidine [
<xref rid="B37-ijms-20-05023" ref-type="bibr">37</xref>
,
<xref rid="B143-ijms-20-05023" ref-type="bibr">143</xref>
,
<xref rid="B144-ijms-20-05023" ref-type="bibr">144</xref>
]. Supplementation of folic or folinic acid may diminish toxicity.
<break></break>
Gastrointestinal symptoms of nausea and diarrhea may be more frequent with oral MTX [
<xref rid="B145-ijms-20-05023" ref-type="bibr">145</xref>
]. Switching from oral to parental administration was shown to significantly decrease the frequency of adverse gastrointestinal events in patients with RA [
<xref rid="B146-ijms-20-05023" ref-type="bibr">146</xref>
,
<xref rid="B147-ijms-20-05023" ref-type="bibr">147</xref>
], suggesting that other mechanisms may account for MTX induced gastrointestinal toxicity.
<break></break>
The pathogenic mechanism underlying gastrointestinal side effects may also be related to the change of plasma homocysteine [
<xref rid="B148-ijms-20-05023" ref-type="bibr">148</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Hematological</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Anaemia;
<break></break>
Leucopenia;
<break></break>
Thrombopenia;
<break></break>
Pancytopenia</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Recently, MTX-induced thrombocytopenia was shown to be mediated by MTX-induced activation of platelet apoptosis via JNK and oxidative stress [
<xref rid="B149-ijms-20-05023" ref-type="bibr">149</xref>
].</td>
</tr>
<tr>
<td rowspan="2" align="center" valign="middle" style="border-bottom:solid thin" colspan="1">Hepatic</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Elevated liver enzymes </td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Long-term MTX administration can cause accumulation of MTX polyglutamates in the liver and decreased folate levels. The depletion of hepatic folate stores by accumulated MTX poly glutamates is one possible toxic effect of MTX on the liver [
<xref rid="B150-ijms-20-05023" ref-type="bibr">150</xref>
]. Folate supplementation has been associated with a reduced incidence of elevated transaminases induced by MTX treatment [
<xref rid="B15-ijms-20-05023" ref-type="bibr">15</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Steatosis, fibrosis, cirrhosis</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">MTX-related hepatic fibrosis may be mediated through an adenosine pathway. MTX was shown to enhance adenosine release from cultured hepatoma (HepG2) cells. Adenosine A2A receptor occupancy stimulates collagen production by hepatic stellate cell lines [
<xref rid="B151-ijms-20-05023" ref-type="bibr">151</xref>
,
<xref rid="B152-ijms-20-05023" ref-type="bibr">152</xref>
]. Unlike wild-type mice, mice deficient for the adenosine A2A receptor or treated with an adenosine A2A receptor antagonist (ZM241385) were protected from developing liver fibrosis when challenged by hepatotoxin (carbon tetrachloride or thiocetamide) [
<xref rid="B151-ijms-20-05023" ref-type="bibr">151</xref>
].
<break></break>
MTX-related liver fibrosis may also be mediated by its capacity to interfere with the generation of methionine from homocysteine. Excess of homocysteine induces endoplasmic reticulum stress promoting fat accumulation in the liver. Homocysteine can also activate hepatic stellate cells and proinflammatory cytokines, leading to liver fibrosis [
<xref rid="B153-ijms-20-05023" ref-type="bibr">153</xref>
,
<xref rid="B154-ijms-20-05023" ref-type="bibr">154</xref>
].
<break></break>
MTX-induced hepatic damage may be related to the generation of reactive oxygen species (ROS). MTX was shown to cause oxidative tissue damage by increasing lipid peroxidation in the liver tissue and decreasing the level of antioxidant enzymes in rats [
<xref rid="B155-ijms-20-05023" ref-type="bibr">155</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Pulmonary</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Interstitial pneumonitis;
<italic>Pneumocystis carinii</italic>
pneumonia; Pulmonary fibrosis</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Pulmonary toxicity has been shown to occur at both high- and low-dose MTX treatment, suggesting an idiosyncratic reaction not linked to folate antagonism [
<xref rid="B49-ijms-20-05023" ref-type="bibr">49</xref>
].
<break></break>
Several mechanisms for the pathogenesis of MTX-induced pneumonitis have been suggested including hypersensitivity, direct drug toxicity to the lung tissue, immunosuppression or altered cytokine expression contributing to the pulmonary inflammatory response and tissue damage [
<xref rid="B156-ijms-20-05023" ref-type="bibr">156</xref>
].
<break></break>
Typical bronchoalveolar lavage and histological findings support the concept that MTX-induced pneumonitis represents a hypersensitivity reaction [
<xref rid="B157-ijms-20-05023" ref-type="bibr">157</xref>
,
<xref rid="B158-ijms-20-05023" ref-type="bibr">158</xref>
,
<xref rid="B159-ijms-20-05023" ref-type="bibr">159</xref>
]. MTX also induces injury to alveolar epithelial walls and pulmonary fibrosis, suggesting a direct drug toxicity route [
<xref rid="B160-ijms-20-05023" ref-type="bibr">160</xref>
].
<break></break>
MTX pulmonary toxicity may be mediated by mitogen-activated protein kinase (MAPK) pathways activation and cytokine release [
<xref rid="B156-ijms-20-05023" ref-type="bibr">156</xref>
].
<break></break>
MTX can compromise the immune response and increase the risk for opportunistic infections due to
<italic>Pneumocystis carinii</italic>
[
<xref rid="B161-ijms-20-05023" ref-type="bibr">161</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Renal</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">A decrease in glomerular filtration rate; Renal insufficiency (only in pre-existing, severely impaired renal function)</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">In contrast to high-dose MTX, which can lead to direct tubulus toxicity and subsequent renal failure, renal toxicities induced by low-dose MTX are rare.
<break></break>
Low dose MTX has been associated with decrease in glomerular filtration rate (GFR) [
<xref rid="B162-ijms-20-05023" ref-type="bibr">162</xref>
,
<xref rid="B163-ijms-20-05023" ref-type="bibr">163</xref>
,
<xref rid="B164-ijms-20-05023" ref-type="bibr">164</xref>
]. MTX and its major metabolite 7-OH-MTX are relatively insoluble in acid urine and may act as a direct toxin on the tubular epithelium, or precipitate within the tubular lumen, which can lead to intratubular obstruction resulting in a decrease in GFR (particularly at high doses) [
<xref rid="B49-ijms-20-05023" ref-type="bibr">49</xref>
,
<xref rid="B165-ijms-20-05023" ref-type="bibr">165</xref>
].
<break></break>
Evidence for a direct toxic effect of MTX on renal tubular cells has been demonstrated [
<xref rid="B166-ijms-20-05023" ref-type="bibr">166</xref>
]; Low doses MTX can induce cell swelling and necrosis in renal tubular cells, which may lead to permanent tubular damage [
<xref rid="B166-ijms-20-05023" ref-type="bibr">166</xref>
].
<break></break>
MTX associated renal toxicity may be explained by an increase in plasma adenosine concentration in extracellular fluid and subsequent activation of A1 receptors in renal tissue, reducing renal blood flow and salt and water excretion [
<xref rid="B167-ijms-20-05023" ref-type="bibr">167</xref>
].
<break></break>
Long duration of low dose MTX administration caused severe kidney injury and renal MTX accumulation in a rat model. 4-hydroxynonenal (4-HNE) and malondialdehyde (MDA), which are reliable oxidative stress markers, were significantly increased in Long-MTX treated rats suggesting that MTX-induced kidney injury may be mediated through an increase in oxidative stress [
<xref rid="B168-ijms-20-05023" ref-type="bibr">168</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Dermatologic </td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Nodulosis (rare); Alopecia; Rash; Anaphylactic reactions</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">MTX-induced nodulosis may be mediated by adenosine through the adenosine A1 receptor [
<xref rid="B169-ijms-20-05023" ref-type="bibr">169</xref>
]. MTX was shown to induce the generation of multinucleated giant cells, as does adenosine A1 receptor occupancy. This effect of MTX was reversed by a specific adenosine A1 receptor antagonist.
<break></break>
Alopecia related to MTX treatment seems to be related to folate antagonism. In low dose MTX treatment, alopecia is rare and generally resolves several months after discontinuation [
<xref rid="B17-ijms-20-05023" ref-type="bibr">17</xref>
,
<xref rid="B170-ijms-20-05023" ref-type="bibr">170</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Central nervous system (CNS)</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Lethargy and fatigue; Headache, vertigo (less frequent)</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Neurotoxicity of MTX may be related to MTX induced adenosine release and accumulation in the CNS. By acting at the A1 receptor on the perifornical lateral hypothalamus, adenosine may regulate wakefulness and somnolence and so potentially explaining asthenia and sleepiness experienced by some patients after MTX intake [
<xref rid="B171-ijms-20-05023" ref-type="bibr">171</xref>
,
<xref rid="B172-ijms-20-05023" ref-type="bibr">172</xref>
].
<break></break>
Other possible mechanisms of MTX-induced neurotoxicity are increased homocysteine levels and their excitatory amino acid neurotransmitter metabolites as homocysteic acid and cysteinesulfinic acid [
<xref rid="B173-ijms-20-05023" ref-type="bibr">173</xref>
] and impairment of biopterin regerenating system in the brain, resulting in a reduced monoamine neurotransmitters availability [
<xref rid="B174-ijms-20-05023" ref-type="bibr">174</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Urogenital</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Teratogenecity; oligospermia; gynecomastia (rare)</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Use of MTX should be avoided before or during pregnancy because of its documented embryotoxicity and teratogenicity [
<xref rid="B175-ijms-20-05023" ref-type="bibr">175</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Musculoskeletal</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Osteopathy; Osteoporosis</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">The effect of low dose MTX on bone was described in rats. Prolonged administration of low dose MTX in rats caused significant osteopenia with reduced osteoblast activity and increased osteoclast recruitment, which results in increased bone resorption [
<xref rid="B176-ijms-20-05023" ref-type="bibr">176</xref>
]. However, no detrimental impact of MTX on the skeleton has been reported in patients treated with low dose MTX. MTX seems to have no clinically significant effect on bone mineral density (BMD) or on the osteoblast lineage [
<xref rid="B177-ijms-20-05023" ref-type="bibr">177</xref>
,
<xref rid="B178-ijms-20-05023" ref-type="bibr">178</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Immunologic</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Opportunistic infections</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">There is a belief amongst rheumatologists that MTX, as an immunosuppressant drug, is asssociated with the development of opportunistic infections. Weekly low-doses MTX can affect T cell activity [
<xref rid="B58-ijms-20-05023" ref-type="bibr">58</xref>
], and cases of Pneumocystis pneumonia, nocardiosis, aspergillum, cryptococcosis, herpes zoster, herpes simplex and listeria-meningitis have been reported [
<xref rid="B170-ijms-20-05023" ref-type="bibr">170</xref>
,
<xref rid="B179-ijms-20-05023" ref-type="bibr">179</xref>
].
<break></break>
Despite some studies suggesting an increased risk of infection with MTX [
<xref rid="B180-ijms-20-05023" ref-type="bibr">180</xref>
,
<xref rid="B181-ijms-20-05023" ref-type="bibr">181</xref>
], several other studies have found that low-dose MTX does not appear to significantly increase the risk of infections in RA patients [
<xref rid="B182-ijms-20-05023" ref-type="bibr">182</xref>
,
<xref rid="B183-ijms-20-05023" ref-type="bibr">183</xref>
,
<xref rid="B184-ijms-20-05023" ref-type="bibr">184</xref>
,
<xref rid="B185-ijms-20-05023" ref-type="bibr">185</xref>
]. This risk appears to be associated with disease activity, comorbidities (diabetes, alcoholism) and the use of glucocorticoids, but not directly with MTX treatment [
<xref rid="B182-ijms-20-05023" ref-type="bibr">182</xref>
]. It is well recognized that RA patients have significant increased risk of infection possibly due to chronic immune activation and inflammation which may impair immune function [
<xref rid="B185-ijms-20-05023" ref-type="bibr">185</xref>
]. An increased risk of infection associated with MTX is possibly offset by the improvement of the immunological function secondary to the control of inflammation [
<xref rid="B185-ijms-20-05023" ref-type="bibr">185</xref>
].</td>
</tr>
<tr>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Others</td>
<td align="center" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Lymphoproliferative disorders</td>
<td align="left" valign="middle" style="border-bottom:solid thin" rowspan="1" colspan="1">Lymphoproliferative disorders occur with increased frequency in RA patients compared to the general population, especially in the setting of high disease activity [
<xref rid="B170-ijms-20-05023" ref-type="bibr">170</xref>
,
<xref rid="B184-ijms-20-05023" ref-type="bibr">184</xref>
,
<xref rid="B186-ijms-20-05023" ref-type="bibr">186</xref>
,
<xref rid="B187-ijms-20-05023" ref-type="bibr">187</xref>
]. A relationship between MTX treatment and the occurrence of lymphoproliferative disorders in RA has been suggested. Long-term MTX therapy was associated with Epstein–Barr virus-related lymphoproliferative disorders with spontaneous regression after MTX withdrawal [
<xref rid="B188-ijms-20-05023" ref-type="bibr">188</xref>
]. Despite its association with Epstein–Barr-associated lymphomas, there is currently no clear evidence that MTX provides additional risk of lymphoproliferative disorders to that of RA itself [
<xref rid="B184-ijms-20-05023" ref-type="bibr">184</xref>
,
<xref rid="B189-ijms-20-05023" ref-type="bibr">189</xref>
].</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</pmc>
</record>

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