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Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin

Purified type A influenza viral hemagglutinin stimulates an in vitro cell-mediated cytotoxic cell response that exhibits a high degree of specificity for the immunizing hemagglutinin. The response magnitude is proportional to the hemagglutinin dose used for stimulation. The lytic activity of the eff...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1979
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184857/
https://www.ncbi.nlm.nih.gov/pubmed/311817
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description Purified type A influenza viral hemagglutinin stimulates an in vitro cell-mediated cytotoxic cell response that exhibits a high degree of specificity for the immunizing hemagglutinin. The response magnitude is proportional to the hemagglutinin dose used for stimulation. The lytic activity of the effector cells is H-2 restricted. Analysis of the specificity of the response indicated that these cytotoxic T cells readily distinguish target cells expressing serologically unrelated hemagglutinin from target cells bearing hemagglutinins serologically related to the stimulating hemagglutinin. Further analysis of the fine specificity of cytotoxic T-cell recognition with serologically cross- reactive type A influenza hemagglutinins revealed a hierarchy of cross- reactivity among these hemagglutinins that was the converse of the serologic hierarchy. These results are discussed in terms of possible differences and similarities in the specificity repertoire of cytotoxic T cells and antibodies. Possible implications of these findings from the standpoint of cytotoxic T-cell induction are also discussed.
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spelling pubmed-21848572008-04-17 Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin J Exp Med Articles Purified type A influenza viral hemagglutinin stimulates an in vitro cell-mediated cytotoxic cell response that exhibits a high degree of specificity for the immunizing hemagglutinin. The response magnitude is proportional to the hemagglutinin dose used for stimulation. The lytic activity of the effector cells is H-2 restricted. Analysis of the specificity of the response indicated that these cytotoxic T cells readily distinguish target cells expressing serologically unrelated hemagglutinin from target cells bearing hemagglutinins serologically related to the stimulating hemagglutinin. Further analysis of the fine specificity of cytotoxic T-cell recognition with serologically cross- reactive type A influenza hemagglutinins revealed a hierarchy of cross- reactivity among these hemagglutinins that was the converse of the serologic hierarchy. These results are discussed in terms of possible differences and similarities in the specificity repertoire of cytotoxic T cells and antibodies. Possible implications of these findings from the standpoint of cytotoxic T-cell induction are also discussed. The Rockefeller University Press 1979-04-01 /pmc/articles/PMC2184857/ /pubmed/311817 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title_full Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title_fullStr Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title_full_unstemmed Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title_short Specificity of cytotoxicity T cells directed to influenza virus hemagglutinin
title_sort specificity of cytotoxicity t cells directed to influenza virus hemagglutinin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184857/
https://www.ncbi.nlm.nih.gov/pubmed/311817