Antigen-dependent proliferation of cloned continuous lines of H-2-restricted influenza virus-specific cytotoxic T lymphocytes.
Identifieur interne : 002708 ( Main/Exploration ); précédent : 002707; suivant : 002709Antigen-dependent proliferation of cloned continuous lines of H-2-restricted influenza virus-specific cytotoxic T lymphocytes.
Auteurs : M E Andrew ; T J BracialeSource :
- Journal of immunology (Baltimore, Md. : 1950) [ 0022-1767 ] ; 1981.
Descripteurs français
- KwdFr :
- Activation des lymphocytes, Animaux, Antigènes, Antigènes H-2, Clones cellulaires (immunologie), Complexe majeur d'histocompatibilité, Cytotoxicité immunologique, Lymphocytes T (immunologie), Lymphokines (pharmacologie), Souris, Souris de lignée BALB C, Souris de lignée C57BL, Virus de la grippe A (immunologie), Épitopes.
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , pharmacology : Lymphokines.
- chemical : Antigens, Epitopes, H-2 Antigens.
- immunology : Clone Cells, Influenza A virus, T-Lymphocytes.
- Animals, Cytotoxicity, Immunologic, Lymphocyte Activation, Major Histocompatibility Complex, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL.
Abstract
The antigenic requirements for in vitro proliferation of several cloned continuous lines of H-2-restricted influenza virus-specific cytotoxic T lymphocytes (CTL) has been examined. The cloned CTL lines were established from individual splenic CTL precursors obtained from A/JAPAN/305/57 (H2N2)-immune F1 (C57BL/6 X BALB/c) donors. The lines were isolated (by limiting dilution in liquid culture) and expanded in the presence of A/JAPAN/305/57-infected irradiated syngeneic (F1) spleen cells and T cell growth factor (TCGF) of rat spleen origin. Optimal proliferation (and long-term in vitro cultivation) of these H-2-restricted CTL lines required both specific antigenic stimulation in the form of virus-infected syngeneic spleen cells and an exogenous source of TCGF. In addition, the antigenic requirements for proliferation of these lines directly reflected the pattern of H-2-restricted influenza virus-specific recognition at the level of target cell recognition and lysis.
PubMed: 6167621
Affiliations:
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Le document en format XML
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<term>Epitopes</term>
<term>H-2 Antigens</term>
<term>Influenza A virus (immunology)</term>
<term>Lymphocyte Activation</term>
<term>Lymphokines (pharmacology)</term>
<term>Major Histocompatibility Complex</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Inbred C57BL</term>
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<term>Complexe majeur d'histocompatibilité</term>
<term>Cytotoxicité immunologique</term>
<term>Lymphocytes T (immunologie)</term>
<term>Lymphokines (pharmacologie)</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Souris de lignée C57BL</term>
<term>Virus de la grippe A (immunologie)</term>
<term>Épitopes</term>
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<term>H-2 Antigens</term>
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<term>Lymphocytes T</term>
<term>Virus de la grippe A</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Clone Cells</term>
<term>Influenza A virus</term>
<term>T-Lymphocytes</term>
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<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Lymphokines</term>
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<term>Cytotoxicity, Immunologic</term>
<term>Lymphocyte Activation</term>
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<term>Mice, Inbred C57BL</term>
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<term>Cytotoxicité immunologique</term>
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<front><div type="abstract" xml:lang="en">The antigenic requirements for in vitro proliferation of several cloned continuous lines of H-2-restricted influenza virus-specific cytotoxic T lymphocytes (CTL) has been examined. The cloned CTL lines were established from individual splenic CTL precursors obtained from A/JAPAN/305/57 (H2N2)-immune F1 (C57BL/6 X BALB/c) donors. The lines were isolated (by limiting dilution in liquid culture) and expanded in the presence of A/JAPAN/305/57-infected irradiated syngeneic (F1) spleen cells and T cell growth factor (TCGF) of rat spleen origin. Optimal proliferation (and long-term in vitro cultivation) of these H-2-restricted CTL lines required both specific antigenic stimulation in the form of virus-infected syngeneic spleen cells and an exogenous source of TCGF. In addition, the antigenic requirements for proliferation of these lines directly reflected the pattern of H-2-restricted influenza virus-specific recognition at the level of target cell recognition and lysis.</div>
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<name sortKey="Braciale, T J" sort="Braciale, T J" uniqKey="Braciale T" first="T J" last="Braciale">T J Braciale</name>
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