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CD4+, CD8+ and CD4- CD8- T cell-subsets can confer protection against Leishmania m. mexicana infection
We studied the role of CD4+, CD8+, CD4- CD8- T cells and IgG anti-Leishmania after infection or vaccination in the CBA/ca mouse. Mice were either infected with L. m. mexicana promastigotes or vaccinated with parasite-membrane antigens incorporated into liposomes. Successfully vaccinated mice were us...
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Published in: | Memórias do Instituto Oswaldo Cruz 1995-01, Vol.90 (1), p.51-58 |
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description | We studied the role of CD4+, CD8+, CD4- CD8- T cells and IgG anti-Leishmania after infection or vaccination in the CBA/ca mouse. Mice were either infected with L. m. mexicana promastigotes or vaccinated with parasite-membrane antigens incorporated into liposomes. Successfully vaccinated mice were used as cell-donors in adoptive transfer experiments. Naive, syngeneic recipients received highly-enriched CD4+, CD8+ or CD4- CD8- T cells from those two set of donors and challenged with live parasites. Our results showed that, both CD4+ and CD8+ T cells from infected or vaccinated donors conferred significant disease-resistance to naive recipients. In addition, adoptive transfer of CD4- CD8- T cells from vaccinated donors significantly delayed lesion growth in recipient mice. We concluded that vaccination of CBA mice correlates with the induction of protective CD4+, CD8+ and CD4- CD8- T cells and the synthesis of IgG anti-Leishmania. |
doi_str_mv | 10.1590/S0074-02761995000100012 |
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Mice were either infected with L. m. mexicana promastigotes or vaccinated with parasite-membrane antigens incorporated into liposomes. Successfully vaccinated mice were used as cell-donors in adoptive transfer experiments. Naive, syngeneic recipients received highly-enriched CD4+, CD8+ or CD4- CD8- T cells from those two set of donors and challenged with live parasites. Our results showed that, both CD4+ and CD8+ T cells from infected or vaccinated donors conferred significant disease-resistance to naive recipients. In addition, adoptive transfer of CD4- CD8- T cells from vaccinated donors significantly delayed lesion growth in recipient mice. We concluded that vaccination of CBA mice correlates with the induction of protective CD4+, CD8+ and CD4- CD8- T cells and the synthesis of IgG anti-Leishmania.</description><identifier>ISSN: 0074-0276</identifier><identifier>ISSN: 1678-8060</identifier><identifier>EISSN: 0074-0276</identifier><identifier>EISSN: 1678-8060</identifier><identifier>DOI: 10.1590/S0074-02761995000100012</identifier><identifier>PMID: 8524085</identifier><language>eng</language><publisher>Brazil: Instituto Oswaldo Cruz, Ministério da Saúde</publisher><subject>AIDS/HIV ; Animals ; CD4-CD8 Ratio ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - parasitology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - parasitology ; Electrophoresis, Polyacrylamide Gel ; Enzyme-Linked Immunosorbent Assay ; Female ; Immunoglobulin G - analysis ; Leishmania m. mexicana ; Leishmania mexicana - immunology ; Leishmaniasis, Cutaneous - immunology ; liposomes monoclonal antibodies ; Male ; Mice ; Mice, Inbred CBA ; PARASITOLOGY ; T cell-subpopulations ; TROPICAL MEDICINE ; Vaccination</subject><ispartof>Memórias do Instituto Oswaldo Cruz, 1995-01, Vol.90 (1), p.51-58</ispartof><rights>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-d06438022136ab5071d8c38db076929ea6ba4e0331fc7673e79a4328419b1abc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,24150,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8524085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lezama-Dávila, C M</creatorcontrib><creatorcontrib>Gallagher, G</creatorcontrib><title>CD4+, CD8+ and CD4- CD8- T cell-subsets can confer protection against Leishmania m. mexicana infection</title><title>Memórias do Instituto Oswaldo Cruz</title><addtitle>Mem Inst Oswaldo Cruz</addtitle><description>We studied the role of CD4+, CD8+, CD4- CD8- T cells and IgG anti-Leishmania after infection or vaccination in the CBA/ca mouse. Mice were either infected with L. m. mexicana promastigotes or vaccinated with parasite-membrane antigens incorporated into liposomes. Successfully vaccinated mice were used as cell-donors in adoptive transfer experiments. Naive, syngeneic recipients received highly-enriched CD4+, CD8+ or CD4- CD8- T cells from those two set of donors and challenged with live parasites. Our results showed that, both CD4+ and CD8+ T cells from infected or vaccinated donors conferred significant disease-resistance to naive recipients. In addition, adoptive transfer of CD4- CD8- T cells from vaccinated donors significantly delayed lesion growth in recipient mice. We concluded that vaccination of CBA mice correlates with the induction of protective CD4+, CD8+ and CD4- CD8- T cells and the synthesis of IgG anti-Leishmania.</description><subject>AIDS/HIV</subject><subject>Animals</subject><subject>CD4-CD8 Ratio</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - parasitology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - parasitology</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Immunoglobulin G - analysis</subject><subject>Leishmania m. mexicana</subject><subject>Leishmania mexicana - immunology</subject><subject>Leishmaniasis, Cutaneous - immunology</subject><subject>liposomes monoclonal antibodies</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>PARASITOLOGY</subject><subject>T cell-subpopulations</subject><subject>TROPICAL MEDICINE</subject><subject>Vaccination</subject><issn>0074-0276</issn><issn>1678-8060</issn><issn>0074-0276</issn><issn>1678-8060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9UU1v1DAQtSpQaQs_ocInLiXL-CNxckTbUiqtxIFytib2pHiVxCVOJPj39X5ohYTEwfIb-703ozeMvRewEmUDn74DGF2ANJVomhIAxO7IM3Zx-nj1F37DLlPaQoaq0ufsvC6lhrq8YN36Vt985Ovb-obj6DPQxa4q-CN31PdFWtpEc-IOR-7i2NHEn6c4k5tDHDk-YRjTzDcU0s8Bx4B8WPGBfofMRx4yf098y1532Cd6d7yv2I8vd4_rr8Xm2_3D-vOmcLqSc-Gh0qoGKYWqsC3BCF87VfsWTNXIhrBqURMoJTpnKqPINKiVrLVoWoGtU1fs4eDrI27t8xQGnP7YiMHuH-L0ZHGag-vJEiAaT4a89Fp5bLxSUJuy884JqCF7rQ5eyQXqo93GZRrz8Hafvf0n-yz4cBDkgH4tlGY7hLQLEUeKS7ImC6ACnYnmQHRTTGmi7jSpALtb739aXB9bLO1A_qQ77lO9AFpvmao</recordid><startdate>19950101</startdate><enddate>19950101</enddate><creator>Lezama-Dávila, C M</creator><creator>Gallagher, G</creator><general>Instituto Oswaldo Cruz, Ministério da Saúde</general><general>Fundação Oswaldo Cruz (FIOCRUZ)</general><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>7X8</scope><scope>GPN</scope><scope>DOA</scope></search><sort><creationdate>19950101</creationdate><title>CD4+, CD8+ and CD4- CD8- T cell-subsets can confer protection against Leishmania m. mexicana infection</title><author>Lezama-Dávila, C M ; Gallagher, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-d06438022136ab5071d8c38db076929ea6ba4e0331fc7673e79a4328419b1abc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>AIDS/HIV</topic><topic>Animals</topic><topic>CD4-CD8 Ratio</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - parasitology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - parasitology</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Immunoglobulin G - analysis</topic><topic>Leishmania m. mexicana</topic><topic>Leishmania mexicana - immunology</topic><topic>Leishmaniasis, Cutaneous - immunology</topic><topic>liposomes monoclonal antibodies</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>PARASITOLOGY</topic><topic>T cell-subpopulations</topic><topic>TROPICAL MEDICINE</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lezama-Dávila, C M</creatorcontrib><creatorcontrib>Gallagher, G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>SciELO</collection><collection>Directory of Open Access Journals</collection><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lezama-Dávila, C M</au><au>Gallagher, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD4+, CD8+ and CD4- CD8- T cell-subsets can confer protection against Leishmania m. mexicana infection</atitle><jtitle>Memórias do Instituto Oswaldo Cruz</jtitle><addtitle>Mem Inst Oswaldo Cruz</addtitle><date>1995-01-01</date><risdate>1995</risdate><volume>90</volume><issue>1</issue><spage>51</spage><epage>58</epage><pages>51-58</pages><issn>0074-0276</issn><issn>1678-8060</issn><eissn>0074-0276</eissn><eissn>1678-8060</eissn><abstract>We studied the role of CD4+, CD8+, CD4- CD8- T cells and IgG anti-Leishmania after infection or vaccination in the CBA/ca mouse. Mice were either infected with L. m. mexicana promastigotes or vaccinated with parasite-membrane antigens incorporated into liposomes. Successfully vaccinated mice were used as cell-donors in adoptive transfer experiments. Naive, syngeneic recipients received highly-enriched CD4+, CD8+ or CD4- CD8- T cells from those two set of donors and challenged with live parasites. Our results showed that, both CD4+ and CD8+ T cells from infected or vaccinated donors conferred significant disease-resistance to naive recipients. In addition, adoptive transfer of CD4- CD8- T cells from vaccinated donors significantly delayed lesion growth in recipient mice. We concluded that vaccination of CBA mice correlates with the induction of protective CD4+, CD8+ and CD4- CD8- T cells and the synthesis of IgG anti-Leishmania.</abstract><cop>Brazil</cop><pub>Instituto Oswaldo Cruz, Ministério da Saúde</pub><pmid>8524085</pmid><doi>10.1590/S0074-02761995000100012</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AIDS/HIV Animals CD4-CD8 Ratio CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - parasitology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - parasitology Electrophoresis, Polyacrylamide Gel Enzyme-Linked Immunosorbent Assay Female Immunoglobulin G - analysis Leishmania m. mexicana Leishmania mexicana - immunology Leishmaniasis, Cutaneous - immunology liposomes monoclonal antibodies Male Mice Mice, Inbred CBA PARASITOLOGY T cell-subpopulations TROPICAL MEDICINE Vaccination |
title | CD4+, CD8+ and CD4- CD8- T cell-subsets can confer protection against Leishmania m. mexicana infection |
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