Regulation of immunoglobulin synthesis by human T cell subsets as defined by anti-D44 monoclonal antibody within the CD4+ and CD8+ subpopulations

In our previous paper, we demonstrated that anti-D44 MAb can, in the presence of complement, eliminate all the allocytotoxicity generated during a mixed lymphocyte reaction without affecting the alloproliferative response. As approximately 70% of CD4+ cells and 30% of CD8+ will be stained with anti-...

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Veröffentlicht in:The Journal of immunology (1950) 1986-02, Vol.136 (4), p.1144-1149
Hauptverfasser: Calvo, CF, Bernard, A, Huet, S, Leroy, E, Boumsell, L, Senik, A
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container_issue 4
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container_title The Journal of immunology (1950)
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creator Calvo, CF
Bernard, A
Huet, S
Leroy, E
Boumsell, L
Senik, A
description In our previous paper, we demonstrated that anti-D44 MAb can, in the presence of complement, eliminate all the allocytotoxicity generated during a mixed lymphocyte reaction without affecting the alloproliferative response. As approximately 70% of CD4+ cells and 30% of CD8+ will be stained with anti-D44 MAb, we researched the functional role of the D44+ and D44- cells in each of these T cell subsets in the PWM-induced antibody response. We found that most of the helper activity for immunoglobulin (Ig) synthesis was mediated by CD4+ D44+ lymphocytes and that virtually all the suppressive activity was mediated by CD8+ D44- lymphocytes. Surprisingly enough, we noticed that the low level of Ig synthesis induced in B cells by CD4+ D44- lymphocytes could be strongly amplified by the addition of radiosensitive CD8+ lymphocytes, suggesting coexisting opposite immunoregulatory functions within the CD8+ T cell subset. These results, together with previous data, indicate that anti-D44 MAb subdivides T cells into subpopulations with distinct functional repertoires: a CD4+ D44+ helper subpopulation, a CD8+ D44+ cytotoxic subpopulation, and a CD8+ D44- suppressor subpopulation.
doi_str_mv 10.4049/jimmunol.136.4.1144
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These results, together with previous data, indicate that anti-D44 MAb subdivides T cells into subpopulations with distinct functional repertoires: a CD4+ D44+ helper subpopulation, a CD8+ D44+ cytotoxic subpopulation, and a CD8+ D44- suppressor subpopulation.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigen-Antibody Reactions</subject><subject>Antigens, Differentiation, T-Lymphocyte</subject><subject>Antigens, Surface - immunology</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immunobiology</topic><topic>Immunoglobulins - biosynthesis</topic><topic>Lymphocyte Activation</topic><topic>Lymphocyte Cooperation</topic><topic>Organs and cells involved in the immune response</topic><topic>Phenotype</topic><topic>Pokeweed Mitogens - pharmacology</topic><topic>T-Lymphocytes - classification</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes, Helper-Inducer - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Calvo, CF</creatorcontrib><creatorcontrib>Bernard, A</creatorcontrib><creatorcontrib>Huet, S</creatorcontrib><creatorcontrib>Leroy, E</creatorcontrib><creatorcontrib>Boumsell, L</creatorcontrib><creatorcontrib>Senik, A</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>Calvo, CF</au><au>Bernard, A</au><au>Huet, S</au><au>Leroy, E</au><au>Boumsell, L</au><au>Senik, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of immunoglobulin synthesis by human T cell subsets as defined by anti-D44 monoclonal antibody within the CD4+ and CD8+ subpopulations</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1986-02-15</date><risdate>1986</risdate><volume>136</volume><issue>4</issue><spage>1144</spage><epage>1149</epage><pages>1144-1149</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>In our previous paper, we demonstrated that anti-D44 MAb can, in the presence of complement, eliminate all the allocytotoxicity generated during a mixed lymphocyte reaction without affecting the alloproliferative response. 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These results, together with previous data, indicate that anti-D44 MAb subdivides T cells into subpopulations with distinct functional repertoires: a CD4+ D44+ helper subpopulation, a CD8+ D44+ cytotoxic subpopulation, and a CD8+ D44- suppressor subpopulation.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>2935572</pmid><doi>10.4049/jimmunol.136.4.1144</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Analysis of the immune response. Humoral and cellular immunity
Antibodies, Monoclonal - immunology
Antigen-Antibody Reactions
Antigens, Differentiation, T-Lymphocyte
Antigens, Surface - immunology
B-Lymphocytes - immunology
B-Lymphocytes - metabolism
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunobiology
Immunoglobulins - biosynthesis
Lymphocyte Activation
Lymphocyte Cooperation
Organs and cells involved in the immune response
Phenotype
Pokeweed Mitogens - pharmacology
T-Lymphocytes - classification
T-Lymphocytes - immunology
T-Lymphocytes, Helper-Inducer - immunology
title Regulation of immunoglobulin synthesis by human T cell subsets as defined by anti-D44 monoclonal antibody within the CD4+ and CD8+ subpopulations
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