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Differential Requirements for Survival and Proliferation of CD8 Naïve or Memory T Cells
The requisite molecular interactions for CD8 T cell memory were determined by comparison of monoclonal naive and memory CD8$^+$ T cells bearing the T cell receptor (TCR) for the HY antigen. Naive T cells required only the right major histocompatibility complex (MHC) class I-restricting molecule to s...
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Published in: | Science (American Association for the Advancement of Science) 1997-06, Vol.276 (5321), p.2057-2062 |
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container_end_page | 2062 |
container_issue | 5321 |
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container_title | Science (American Association for the Advancement of Science) |
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creator | Tanchot, Corinne Lemonnier, François A. Pérarnau, Beatrice Freitas, Antonio A. Rocha, Benedita |
description | The requisite molecular interactions for CD8 T cell memory were determined by comparison of monoclonal naive and memory CD8$^+$ T cells bearing the T cell receptor (TCR) for the HY antigen. Naive T cells required only the right major histocompatibility complex (MHC) class I-restricting molecule to survive; to expand, they also needed antigen. In contrast, for survival, memory cells did not require the restricting MHC allele, but needed only a nonspecific class I; for expansion the correct class I, but not antigen, was required. Thus, maintenance of CD8 T cell memory still required TCR-MHC class I interactions, but memory T cells may have a lower functional activation threshold that facilitates secondary responses. |
doi_str_mv | 10.1126/science.276.5321.2057 |
format | article |
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Naive T cells required only the right major histocompatibility complex (MHC) class I-restricting molecule to survive; to expand, they also needed antigen. In contrast, for survival, memory cells did not require the restricting MHC allele, but needed only a nonspecific class I; for expansion the correct class I, but not antigen, was required. Thus, maintenance of CD8 T cell memory still required TCR-MHC class I interactions, but memory T cells may have a lower functional activation threshold that facilitates secondary responses.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.276.5321.2057</identifier><identifier>PMID: 9197272</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: American Society for the Advancement of Science</publisher><subject>Adoptive Transfer ; AIDS/HIV ; Animals ; Antigen receptors, T cell ; Antigens ; Biological and medical sciences ; CD8-Positive T-Lymphocytes ; CD8-Positive T-Lymphocytes - cytology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - transplantation ; Cell differentiation ; Cell Division ; Cell lines ; Cell Survival ; Cellular biology ; Chimeras ; Differentiation ; Female ; Females ; Fundamental and applied biological sciences. 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Naive T cells required only the right major histocompatibility complex (MHC) class I-restricting molecule to survive; to expand, they also needed antigen. In contrast, for survival, memory cells did not require the restricting MHC allele, but needed only a nonspecific class I; for expansion the correct class I, but not antigen, was required. Thus, maintenance of CD8 T cell memory still required TCR-MHC class I interactions, but memory T cells may have a lower functional activation threshold that facilitates secondary responses.</description><subject>Adoptive Transfer</subject><subject>AIDS/HIV</subject><subject>Animals</subject><subject>Antigen receptors, T cell</subject><subject>Antigens</subject><subject>Biological and medical sciences</subject><subject>CD8-Positive T-Lymphocytes</subject><subject>CD8-Positive T-Lymphocytes - cytology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - transplantation</subject><subject>Cell differentiation</subject><subject>Cell Division</subject><subject>Cell lines</subject><subject>Cell Survival</subject><subject>Cellular biology</subject><subject>Chimeras</subject><subject>Differentiation</subject><subject>Female</subject><subject>Females</subject><subject>Fundamental and applied biological sciences. 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cytology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - transplantation</topic><topic>Cell differentiation</topic><topic>Cell Division</topic><topic>Cell lines</topic><topic>Cell Survival</topic><topic>Cellular biology</topic><topic>Chimeras</topic><topic>Differentiation</topic><topic>Female</topic><topic>Females</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>H-2 Antigens</topic><topic>H-2 Antigens - immunology</topic><topic>H-Y Antigen</topic><topic>H-Y Antigen - immunology</topic><topic>Histocompatibility Antigen H-2D</topic><topic>Immunobiology</topic><topic>Immunologic Memory</topic><topic>Immunology</topic><topic>Life Sciences</topic><topic>Lymph nodes</topic><topic>Lymphocyte Activation</topic><topic>Lymphoid cells: ontogeny, maturation, markers, receptors, circulation and recirculation</topic><topic>Male</topic><topic>Males</topic><topic>Memory</topic><topic>Messenger RNA</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Organ donation</topic><topic>Persistence</topic><topic>Receptors</topic><topic>Receptors, Antigen, T-Cell, alpha-beta</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - immunology</topic><topic>Spleen cells</topic><topic>Studies</topic><topic>T cell antigen receptors</topic><topic>T cells</topic><topic>T lymphocytes</topic><topic>T-Lymphocyte Subsets</topic><topic>T-Lymphocyte Subsets - 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Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanchot, Corinne</au><au>Lemonnier, François A.</au><au>Pérarnau, Beatrice</au><au>Freitas, Antonio A.</au><au>Rocha, Benedita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Requirements for Survival and Proliferation of CD8 Naïve or Memory T Cells</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1997-06-27</date><risdate>1997</risdate><volume>276</volume><issue>5321</issue><spage>2057</spage><epage>2062</epage><pages>2057-2062</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>The requisite molecular interactions for CD8 T cell memory were determined by comparison of monoclonal naive and memory CD8$^+$ T cells bearing the T cell receptor (TCR) for the HY antigen. Naive T cells required only the right major histocompatibility complex (MHC) class I-restricting molecule to survive; to expand, they also needed antigen. In contrast, for survival, memory cells did not require the restricting MHC allele, but needed only a nonspecific class I; for expansion the correct class I, but not antigen, was required. Thus, maintenance of CD8 T cell memory still required TCR-MHC class I interactions, but memory T cells may have a lower functional activation threshold that facilitates secondary responses.</abstract><cop>Washington, DC</cop><pub>American Society for the Advancement of Science</pub><pmid>9197272</pmid><doi>10.1126/science.276.5321.2057</doi><tpages>6</tpages></addata></record> |
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recordid | cdi_hal_primary_oai_HAL_pasteur_00327781v1 |
source | American Association for the Advancement of Science; Education Collection (Proquest) (PQ_SDU_P3); Social Science Premium Collection (Proquest) (PQ_SDU_P3); Alma/SFX Local Collection; JSTOR |
subjects | Adoptive Transfer AIDS/HIV Animals Antigen receptors, T cell Antigens Biological and medical sciences CD8-Positive T-Lymphocytes CD8-Positive T-Lymphocytes - cytology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - transplantation Cell differentiation Cell Division Cell lines Cell Survival Cellular biology Chimeras Differentiation Female Females Fundamental and applied biological sciences. Psychology Fundamental immunology H-2 Antigens H-2 Antigens - immunology H-Y Antigen H-Y Antigen - immunology Histocompatibility Antigen H-2D Immunobiology Immunologic Memory Immunology Life Sciences Lymph nodes Lymphocyte Activation Lymphoid cells: ontogeny, maturation, markers, receptors, circulation and recirculation Male Males Memory Messenger RNA Mice Mice, Inbred C57BL Mice, Transgenic Organ donation Persistence Receptors Receptors, Antigen, T-Cell, alpha-beta Receptors, Antigen, T-Cell, alpha-beta - immunology Spleen cells Studies T cell antigen receptors T cells T lymphocytes T-Lymphocyte Subsets T-Lymphocyte Subsets - cytology T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - transplantation |
title | Differential Requirements for Survival and Proliferation of CD8 Naïve or Memory T Cells |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T17%3A01%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20Requirements%20for%20Survival%20and%20Proliferation%20of%20CD8%20Na%C3%AFve%20or%20Memory%20T%20Cells&rft.jtitle=Science%20(American%20Association%20for%20the%20Advancement%20of%20Science)&rft.au=Tanchot,%20Corinne&rft.date=1997-06-27&rft.volume=276&rft.issue=5321&rft.spage=2057&rft.epage=2062&rft.pages=2057-2062&rft.issn=0036-8075&rft.eissn=1095-9203&rft.coden=SCIEAS&rft_id=info:doi/10.1126/science.276.5321.2057&rft_dat=%3Cgale_hal_p%3EA19605423%3C/gale_hal_p%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c778t-1cb4b88439cfc6e01f9f5ed38c6a26d775316a6e8daab91169910a3f12f933443%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=213574282&rft_id=info:pmid/9197272&rft_galeid=A19605423&rft_jstor_id=2892986&rfr_iscdi=true |