Effect of methotrexate on Th1 and Th2 immune responses in mice

ABSTRACT We investigated the effect of the anti‐rheumatic drug methotrexate (MTX) on Th1 and Th2 immune responses in mice. For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2003-12, Vol.55 (12), p.1661-1666
Hauptverfasser: Yamaki, Kouya, Uchida, Hiroyuki, Harada, Yoshiki, Li, Xiaojuan, Yanagisawa, Rie, Takano, Hirohisa, Hayashi, Hideyuki, Taneda, Shinji, Mori, Yoki, Yoshino, Shin
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container_end_page 1666
container_issue 12
container_start_page 1661
container_title Journal of pharmacy and pharmacology
container_volume 55
creator Yamaki, Kouya
Uchida, Hiroyuki
Harada, Yoshiki
Li, Xiaojuan
Yanagisawa, Rie
Takano, Hirohisa
Hayashi, Hideyuki
Taneda, Shinji
Mori, Yoki
Yoshino, Shin
description ABSTRACT We investigated the effect of the anti‐rheumatic drug methotrexate (MTX) on Th1 and Th2 immune responses in mice. For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of MTX were orally administered daily from days 0 to 20. On day 21, anti‐OVA IgG2a and interferon‐γ (IFN‐γ) as indicators of Th1 responses and anti‐OVA IgG1 and interleukin‐10 (IL‐10) as those of Th2 responses were measured. The results showed that treatment with MTX was followed by decreases in OVA‐specific IgG and proliferation of spleen cells to the antigen. The anti‐rheumatic drug inhibited both anti‐OVA IgG2a and IgG1production, although the inhibitory effect of MTX on the antigen‐specific IgG2a production appeared to be greater than that on IgG1 production. IFN‐γ, but not IL‐10, secretion was markedly downregulated by MTX. Administration of MTX resulted in suppression of antigen (OVA)‐induced arthritis in mice. The suppression of the joint inflammation by MTX was associated with inhibition of OVA‐specific proliferative responses of spleen cells, anti‐OVA IgG, IgG2a and IgG1 production, and IFN‐γ and IL‐10 secretion, although more pronounced decreases in IgG2a and IFN‐γ were observed compared with those in IgG1 and IL‐10 in MTX‐treated mice. These results indicate that MTX appears to suppress Th1 and, to a lesser extent, Th2 immune responses and its anti‐arthritic effect on human rheumatoid arthritis might be at least in part explained by down‐regulation of Th1 responses involved in the disease.
doi_str_mv 10.1211/0022357022269
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For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of MTX were orally administered daily from days 0 to 20. On day 21, anti‐OVA IgG2a and interferon‐γ (IFN‐γ) as indicators of Th1 responses and anti‐OVA IgG1 and interleukin‐10 (IL‐10) as those of Th2 responses were measured. The results showed that treatment with MTX was followed by decreases in OVA‐specific IgG and proliferation of spleen cells to the antigen. The anti‐rheumatic drug inhibited both anti‐OVA IgG2a and IgG1production, although the inhibitory effect of MTX on the antigen‐specific IgG2a production appeared to be greater than that on IgG1 production. IFN‐γ, but not IL‐10, secretion was markedly downregulated by MTX. Administration of MTX resulted in suppression of antigen (OVA)‐induced arthritis in mice. The suppression of the joint inflammation by MTX was associated with inhibition of OVA‐specific proliferative responses of spleen cells, anti‐OVA IgG, IgG2a and IgG1 production, and IFN‐γ and IL‐10 secretion, although more pronounced decreases in IgG2a and IFN‐γ were observed compared with those in IgG1 and IL‐10 in MTX‐treated mice. These results indicate that MTX appears to suppress Th1 and, to a lesser extent, Th2 immune responses and its anti‐arthritic effect on human rheumatoid arthritis might be at least in part explained by down‐regulation of Th1 responses involved in the disease.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/0022357022269</identifier><identifier>PMID: 14738593</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Animals ; Antirheumatic Agents - pharmacology ; Female ; Immune System - drug effects ; Interferon-gamma - secretion ; Methotrexate - pharmacology ; Mice ; Mice, Inbred DBA ; Ovalbumin - immunology ; Spleen - drug effects ; Spleen - immunology ; Spleen - metabolism ; Th1 Cells - drug effects ; Th1 Cells - immunology ; Th2 Cells - drug effects ; Th2 Cells - immunology</subject><ispartof>Journal of pharmacy and pharmacology, 2003-12, Vol.55 (12), p.1661-1666</ispartof><rights>2003 Royal Pharmaceutical Society of Great Britain</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4683-2112234722010769be766cc9bff5b1e30a99eadf0adf3dd9f038d17958cf9013</citedby><cites>FETCH-LOGICAL-c4683-2112234722010769be766cc9bff5b1e30a99eadf0adf3dd9f038d17958cf9013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1211%2F0022357022269$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1211%2F0022357022269$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14738593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamaki, Kouya</creatorcontrib><creatorcontrib>Uchida, Hiroyuki</creatorcontrib><creatorcontrib>Harada, Yoshiki</creatorcontrib><creatorcontrib>Li, Xiaojuan</creatorcontrib><creatorcontrib>Yanagisawa, Rie</creatorcontrib><creatorcontrib>Takano, Hirohisa</creatorcontrib><creatorcontrib>Hayashi, Hideyuki</creatorcontrib><creatorcontrib>Taneda, Shinji</creatorcontrib><creatorcontrib>Mori, Yoki</creatorcontrib><creatorcontrib>Yoshino, Shin</creatorcontrib><title>Effect of methotrexate on Th1 and Th2 immune responses in mice</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>ABSTRACT We investigated the effect of the anti‐rheumatic drug methotrexate (MTX) on Th1 and Th2 immune responses in mice. For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of MTX were orally administered daily from days 0 to 20. On day 21, anti‐OVA IgG2a and interferon‐γ (IFN‐γ) as indicators of Th1 responses and anti‐OVA IgG1 and interleukin‐10 (IL‐10) as those of Th2 responses were measured. The results showed that treatment with MTX was followed by decreases in OVA‐specific IgG and proliferation of spleen cells to the antigen. The anti‐rheumatic drug inhibited both anti‐OVA IgG2a and IgG1production, although the inhibitory effect of MTX on the antigen‐specific IgG2a production appeared to be greater than that on IgG1 production. IFN‐γ, but not IL‐10, secretion was markedly downregulated by MTX. Administration of MTX resulted in suppression of antigen (OVA)‐induced arthritis in mice. The suppression of the joint inflammation by MTX was associated with inhibition of OVA‐specific proliferative responses of spleen cells, anti‐OVA IgG, IgG2a and IgG1 production, and IFN‐γ and IL‐10 secretion, although more pronounced decreases in IgG2a and IFN‐γ were observed compared with those in IgG1 and IL‐10 in MTX‐treated mice. These results indicate that MTX appears to suppress Th1 and, to a lesser extent, Th2 immune responses and its anti‐arthritic effect on human rheumatoid arthritis might be at least in part explained by down‐regulation of Th1 responses involved in the disease.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antirheumatic Agents - pharmacology</subject><subject>Female</subject><subject>Immune System - drug effects</subject><subject>Interferon-gamma - secretion</subject><subject>Methotrexate - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred DBA</subject><subject>Ovalbumin - immunology</subject><subject>Spleen - drug effects</subject><subject>Spleen - immunology</subject><subject>Spleen - metabolism</subject><subject>Th1 Cells - drug effects</subject><subject>Th1 Cells - immunology</subject><subject>Th2 Cells - drug effects</subject><subject>Th2 Cells - immunology</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkL1PwzAQxS0EoqUwsiJPbAF_JHG8ICFUWlAFFapgtBznrAaapNiJaP97XLWiYoHh7ob73fPzQ-ickivKKL0mhDGeiNBZKg9Qn5GYRYIm2SHqb3ZRWPIeOvH-nRAi0jQ9Rj0aC54lkvfRzdBaMC1uLK6gnTetg5VuATc1ns0p1nURJsNlVXU1YAd-2dQePC5rXJUGTtGR1QsPZ7s5QLP74exuHE2eRw93t5PIxGnGo2A0uIwFY4QGDzKHYMQYmVub5BQ40VKCLiwJxYtCWsKzggqZZMZKQvkAXW5ll6757MC3qiq9gcVC19B0XoX_UkEJ_xcM79OYxTKA0RY0rvHegVVLV1barRUlahOs-hVs4C92wl1eQbGnd0kGgG-Br3IB67_V1ON0PGXhcm-j9C2sfq60-1Cp4CJRb08j9fLKU0EmVCX8G3vojaY</recordid><startdate>200312</startdate><enddate>200312</enddate><creator>Yamaki, Kouya</creator><creator>Uchida, Hiroyuki</creator><creator>Harada, Yoshiki</creator><creator>Li, Xiaojuan</creator><creator>Yanagisawa, Rie</creator><creator>Takano, Hirohisa</creator><creator>Hayashi, Hideyuki</creator><creator>Taneda, Shinji</creator><creator>Mori, Yoki</creator><creator>Yoshino, Shin</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200312</creationdate><title>Effect of methotrexate on Th1 and Th2 immune responses in mice</title><author>Yamaki, Kouya ; Uchida, Hiroyuki ; Harada, Yoshiki ; Li, Xiaojuan ; Yanagisawa, Rie ; Takano, Hirohisa ; Hayashi, Hideyuki ; Taneda, Shinji ; Mori, Yoki ; Yoshino, Shin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4683-2112234722010769be766cc9bff5b1e30a99eadf0adf3dd9f038d17958cf9013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antirheumatic Agents - pharmacology</topic><topic>Female</topic><topic>Immune System - drug effects</topic><topic>Interferon-gamma - secretion</topic><topic>Methotrexate - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred DBA</topic><topic>Ovalbumin - immunology</topic><topic>Spleen - drug effects</topic><topic>Spleen - immunology</topic><topic>Spleen - metabolism</topic><topic>Th1 Cells - drug effects</topic><topic>Th1 Cells - immunology</topic><topic>Th2 Cells - drug effects</topic><topic>Th2 Cells - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaki, Kouya</creatorcontrib><creatorcontrib>Uchida, Hiroyuki</creatorcontrib><creatorcontrib>Harada, Yoshiki</creatorcontrib><creatorcontrib>Li, Xiaojuan</creatorcontrib><creatorcontrib>Yanagisawa, Rie</creatorcontrib><creatorcontrib>Takano, Hirohisa</creatorcontrib><creatorcontrib>Hayashi, Hideyuki</creatorcontrib><creatorcontrib>Taneda, Shinji</creatorcontrib><creatorcontrib>Mori, Yoki</creatorcontrib><creatorcontrib>Yoshino, Shin</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamaki, Kouya</au><au>Uchida, Hiroyuki</au><au>Harada, Yoshiki</au><au>Li, Xiaojuan</au><au>Yanagisawa, Rie</au><au>Takano, Hirohisa</au><au>Hayashi, Hideyuki</au><au>Taneda, Shinji</au><au>Mori, Yoki</au><au>Yoshino, Shin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of methotrexate on Th1 and Th2 immune responses in mice</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2003-12</date><risdate>2003</risdate><volume>55</volume><issue>12</issue><spage>1661</spage><epage>1666</epage><pages>1661-1666</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><abstract>ABSTRACT We investigated the effect of the anti‐rheumatic drug methotrexate (MTX) on Th1 and Th2 immune responses in mice. For this investigation, mice were immunized subcutaneously at the base of the tail with ovalbumin (OVA) emulsified with complete Freund's adjuvant (day 0). Varying doses of MTX were orally administered daily from days 0 to 20. On day 21, anti‐OVA IgG2a and interferon‐γ (IFN‐γ) as indicators of Th1 responses and anti‐OVA IgG1 and interleukin‐10 (IL‐10) as those of Th2 responses were measured. The results showed that treatment with MTX was followed by decreases in OVA‐specific IgG and proliferation of spleen cells to the antigen. The anti‐rheumatic drug inhibited both anti‐OVA IgG2a and IgG1production, although the inhibitory effect of MTX on the antigen‐specific IgG2a production appeared to be greater than that on IgG1 production. IFN‐γ, but not IL‐10, secretion was markedly downregulated by MTX. Administration of MTX resulted in suppression of antigen (OVA)‐induced arthritis in mice. The suppression of the joint inflammation by MTX was associated with inhibition of OVA‐specific proliferative responses of spleen cells, anti‐OVA IgG, IgG2a and IgG1 production, and IFN‐γ and IL‐10 secretion, although more pronounced decreases in IgG2a and IFN‐γ were observed compared with those in IgG1 and IL‐10 in MTX‐treated mice. These results indicate that MTX appears to suppress Th1 and, to a lesser extent, Th2 immune responses and its anti‐arthritic effect on human rheumatoid arthritis might be at least in part explained by down‐regulation of Th1 responses involved in the disease.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>14738593</pmid><doi>10.1211/0022357022269</doi><tpages>6</tpages></addata></record>
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subjects Administration, Oral
Animals
Antirheumatic Agents - pharmacology
Female
Immune System - drug effects
Interferon-gamma - secretion
Methotrexate - pharmacology
Mice
Mice, Inbred DBA
Ovalbumin - immunology
Spleen - drug effects
Spleen - immunology
Spleen - metabolism
Th1 Cells - drug effects
Th1 Cells - immunology
Th2 Cells - drug effects
Th2 Cells - immunology
title Effect of methotrexate on Th1 and Th2 immune responses in mice
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