Polypeptide specificities of measles virus-reactive T cell lines and clones derived from a patient with multiple sclerosis
Eleven cloned and uncloned measles virus-specific T cell lines were generated from peripheral blood lymphocytes obtained from a patient with multiple sclerosis and were assayed for measles polypeptide specificity. Three clones reacted specifically with the fusion (F) protein and one recognized the h...
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Veröffentlicht in: | The Journal of immunology (1950) 1986-10, Vol.137 (7), p.2190-2194 |
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container_title | The Journal of immunology (1950) |
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creator | Richert, JR Rose, JW Reuben-Burnside, C Kearns, MC Jacobson, S Mingioli, ES Hartzman, RJ McFarland, HF McFarlin, DE |
description | Eleven cloned and uncloned measles virus-specific T cell lines were generated from peripheral blood lymphocytes obtained from a patient with multiple sclerosis and were assayed for measles polypeptide specificity. Three clones reacted specifically with the fusion (F) protein and one recognized the hemagglutinin (HA). Two reacted with whole virus but not with any of the purified proteins. Five cell lines proliferated in response to multiple measles polypeptides. The addition of anti-HA or anti-F monoclonal antibodies to two of the multispecific cell lines each resulted in partial suppression of the proliferative response to whole virus by the cell lines. Two of the three F-reactive clones recognized antigen in association with a subgroup of HLA-DR4; the third responded to F only in the presence of autologous antigen-presenting cells. Of the two clones that reacted only with whole virus, one was restricted to DP3 and one to autologous cells. The HA-specific clone was DP3 restricted. Several cell lines recognized multiple measles polypeptides in association with a single HLA antigen. Recognition of individual measles polypeptides does not segregate with specific genetic restriction elements. |
doi_str_mv | 10.4049/jimmunol.137.7.2190 |
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Three clones reacted specifically with the fusion (F) protein and one recognized the hemagglutinin (HA). Two reacted with whole virus but not with any of the purified proteins. Five cell lines proliferated in response to multiple measles polypeptides. The addition of anti-HA or anti-F monoclonal antibodies to two of the multispecific cell lines each resulted in partial suppression of the proliferative response to whole virus by the cell lines. Two of the three F-reactive clones recognized antigen in association with a subgroup of HLA-DR4; the third responded to F only in the presence of autologous antigen-presenting cells. Of the two clones that reacted only with whole virus, one was restricted to DP3 and one to autologous cells. The HA-specific clone was DP3 restricted. Several cell lines recognized multiple measles polypeptides in association with a single HLA antigen. Recognition of individual measles polypeptides does not segregate with specific genetic restriction elements.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.137.7.2190</identifier><identifier>PMID: 2428863</identifier><identifier>CODEN: JOIMA3</identifier><language>eng</language><publisher>Bethesda, MD: Am Assoc Immnol</publisher><subject>Antigens, Viral - immunology ; Biological and medical sciences ; Capsid - immunology ; Clone Cells - immunology ; Epitopes ; Hemagglutinins, Viral - immunology ; Humans ; Lymphocyte Activation ; Measles virus - immunology ; Medical sciences ; Multiple Sclerosis - immunology ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology ; Phosphoproteins - immunology ; T-Lymphocytes - immunology ; Viral Core Proteins - immunology ; Viral Fusion Proteins - immunology ; Viral Proteins - immunology</subject><ispartof>The Journal of immunology (1950), 1986-10, Vol.137 (7), p.2190-2194</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-c6fd320f94c459028a2a41cccb61a8528c25b7e4a84896ebde8baf3c14bd5bc23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7928024$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2428863$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Richert, JR</creatorcontrib><creatorcontrib>Rose, JW</creatorcontrib><creatorcontrib>Reuben-Burnside, C</creatorcontrib><creatorcontrib>Kearns, MC</creatorcontrib><creatorcontrib>Jacobson, S</creatorcontrib><creatorcontrib>Mingioli, ES</creatorcontrib><creatorcontrib>Hartzman, RJ</creatorcontrib><creatorcontrib>McFarland, HF</creatorcontrib><creatorcontrib>McFarlin, DE</creatorcontrib><title>Polypeptide specificities of measles virus-reactive T cell lines and clones derived from a patient with multiple sclerosis</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Eleven cloned and uncloned measles virus-specific T cell lines were generated from peripheral blood lymphocytes obtained from a patient with multiple sclerosis and were assayed for measles polypeptide specificity. Three clones reacted specifically with the fusion (F) protein and one recognized the hemagglutinin (HA). Two reacted with whole virus but not with any of the purified proteins. Five cell lines proliferated in response to multiple measles polypeptides. The addition of anti-HA or anti-F monoclonal antibodies to two of the multispecific cell lines each resulted in partial suppression of the proliferative response to whole virus by the cell lines. Two of the three F-reactive clones recognized antigen in association with a subgroup of HLA-DR4; the third responded to F only in the presence of autologous antigen-presenting cells. Of the two clones that reacted only with whole virus, one was restricted to DP3 and one to autologous cells. The HA-specific clone was DP3 restricted. Several cell lines recognized multiple measles polypeptides in association with a single HLA antigen. Recognition of individual measles polypeptides does not segregate with specific genetic restriction elements.</description><subject>Antigens, Viral - immunology</subject><subject>Biological and medical sciences</subject><subject>Capsid - immunology</subject><subject>Clone Cells - immunology</subject><subject>Epitopes</subject><subject>Hemagglutinins, Viral - immunology</subject><subject>Humans</subject><subject>Lymphocyte Activation</subject><subject>Measles virus - immunology</subject><subject>Medical sciences</subject><subject>Multiple Sclerosis - immunology</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><subject>Phosphoproteins - immunology</subject><subject>T-Lymphocytes - immunology</subject><subject>Viral Core Proteins - immunology</subject><subject>Viral Fusion Proteins - immunology</subject><subject>Viral Proteins - immunology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkU9v1DAQxS0EKtvCJ0BIPiB6ymI7ju0cUcU_qRIcytlyJhPWlZ0EO2lUPj1e7VJxmpHemzf2bwh5w9leMtl-uPcxruMU9rzWe70XvGXPyI43DauUYuo52TEmRMW10i_JZc73jDHFhLwgF0IKY1S9I39-TOFxxnnxPdI8I_jBg188ZjoNNKLLobQPPq25Suhg8Q9I7yhgCDT4sWhu7CmE6dj2mIrc0yFNkTo6u5IzLnTzy4HGNSx-DmUJBExT9vkVeTG4kPH1uV6Rn58_3d18rW6_f_l28_G2AsnUUoEa-lqwoZUgm5YJ44STHAA6xZ1phAHRdBqlM9K0CrseTeeGGrjs-qYDUV-R96fcOU2_V8yLjT4fP-BGnNZstWZKMC2LsT4ZobwvJxzsnHx06dFyZo_E7T_ithC32h6Jl6m35_i1i9g_zZwRF_3dWXcZXBiSG8HnJ5tuhSk3Kbbrk-3gfx02n9Dm6EIoodxu2_bfwr8voZxJ</recordid><startdate>19861001</startdate><enddate>19861001</enddate><creator>Richert, JR</creator><creator>Rose, JW</creator><creator>Reuben-Burnside, C</creator><creator>Kearns, MC</creator><creator>Jacobson, S</creator><creator>Mingioli, ES</creator><creator>Hartzman, RJ</creator><creator>McFarland, HF</creator><creator>McFarlin, DE</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>19861001</creationdate><title>Polypeptide specificities of measles virus-reactive T cell lines and clones derived from a patient with multiple sclerosis</title><author>Richert, JR ; Rose, JW ; Reuben-Burnside, C ; Kearns, MC ; Jacobson, S ; Mingioli, ES ; Hartzman, RJ ; McFarland, HF ; McFarlin, DE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-c6fd320f94c459028a2a41cccb61a8528c25b7e4a84896ebde8baf3c14bd5bc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Antigens, Viral - immunology</topic><topic>Biological and medical sciences</topic><topic>Capsid - immunology</topic><topic>Clone Cells - immunology</topic><topic>Epitopes</topic><topic>Hemagglutinins, Viral - immunology</topic><topic>Humans</topic><topic>Lymphocyte Activation</topic><topic>Measles virus - immunology</topic><topic>Medical sciences</topic><topic>Multiple Sclerosis - immunology</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><topic>Phosphoproteins - immunology</topic><topic>T-Lymphocytes - immunology</topic><topic>Viral Core Proteins - immunology</topic><topic>Viral Fusion Proteins - immunology</topic><topic>Viral Proteins - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Richert, JR</creatorcontrib><creatorcontrib>Rose, JW</creatorcontrib><creatorcontrib>Reuben-Burnside, C</creatorcontrib><creatorcontrib>Kearns, MC</creatorcontrib><creatorcontrib>Jacobson, S</creatorcontrib><creatorcontrib>Mingioli, ES</creatorcontrib><creatorcontrib>Hartzman, RJ</creatorcontrib><creatorcontrib>McFarland, HF</creatorcontrib><creatorcontrib>McFarlin, DE</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Richert, JR</au><au>Rose, JW</au><au>Reuben-Burnside, C</au><au>Kearns, MC</au><au>Jacobson, S</au><au>Mingioli, ES</au><au>Hartzman, RJ</au><au>McFarland, HF</au><au>McFarlin, DE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polypeptide specificities of measles virus-reactive T cell lines and clones derived from a patient with multiple sclerosis</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1986-10-01</date><risdate>1986</risdate><volume>137</volume><issue>7</issue><spage>2190</spage><epage>2194</epage><pages>2190-2194</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>Eleven cloned and uncloned measles virus-specific T cell lines were generated from peripheral blood lymphocytes obtained from a patient with multiple sclerosis and were assayed for measles polypeptide specificity. Three clones reacted specifically with the fusion (F) protein and one recognized the hemagglutinin (HA). Two reacted with whole virus but not with any of the purified proteins. Five cell lines proliferated in response to multiple measles polypeptides. The addition of anti-HA or anti-F monoclonal antibodies to two of the multispecific cell lines each resulted in partial suppression of the proliferative response to whole virus by the cell lines. Two of the three F-reactive clones recognized antigen in association with a subgroup of HLA-DR4; the third responded to F only in the presence of autologous antigen-presenting cells. Of the two clones that reacted only with whole virus, one was restricted to DP3 and one to autologous cells. The HA-specific clone was DP3 restricted. Several cell lines recognized multiple measles polypeptides in association with a single HLA antigen. Recognition of individual measles polypeptides does not segregate with specific genetic restriction elements.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>2428863</pmid><doi>10.4049/jimmunol.137.7.2190</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, Viral - immunology Biological and medical sciences Capsid - immunology Clone Cells - immunology Epitopes Hemagglutinins, Viral - immunology Humans Lymphocyte Activation Measles virus - immunology Medical sciences Multiple Sclerosis - immunology Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Neurology Phosphoproteins - immunology T-Lymphocytes - immunology Viral Core Proteins - immunology Viral Fusion Proteins - immunology Viral Proteins - immunology |
title | Polypeptide specificities of measles virus-reactive T cell lines and clones derived from a patient with multiple sclerosis |
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