Rapid effector function in CD8+ memory T cells.

The nature of the CD8+ T cells that underlie antiviral protective immunological memory in vivo is unclear. We have characterized peptide-specific CD8+ T lymphocytes directly ex vivo from peripheral blood in humans with past exposure to influenza virus, using single cell interferon gamma (IFN-gamma)...

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Huvudupphovsmän: Lalvani, A, Brookes, R, Hambleton, S, Britton, W, Hill, A, McMichael, A
Materialtyp: Journal article
Språk:English
Publicerad: 1997
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author Lalvani, A
Brookes, R
Hambleton, S
Britton, W
Hill, A
McMichael, A
author_facet Lalvani, A
Brookes, R
Hambleton, S
Britton, W
Hill, A
McMichael, A
author_sort Lalvani, A
collection OXFORD
description The nature of the CD8+ T cells that underlie antiviral protective immunological memory in vivo is unclear. We have characterized peptide-specific CD8+ T lymphocytes directly ex vivo from peripheral blood in humans with past exposure to influenza virus, using single cell interferon gamma (IFN-gamma) release as a measure of effector function. In individuals in the memory state with respect to influenza virus infection, unrestimulated antigen-specific CD8+ T cells displayed IFN-gamma release within 6 h of antigen contact, identifying a population of memory CD8+ T cells that exhibit effector function without needing to divide and differentiate over several days. We have quantified circulating CD8+ effector T cells specific for six different MHC class I-restricted influenza virus epitopes. Enumeration of these CD8+ T cells gives frequencies of peptide-specific T cells that correlate with, but are in general severalfold higher than, CTL precursor frequencies derived from limiting dilution analysis, indicating that this novel population of memory CD8+ T cells has hitherto been undetected by standard means. The phenotype of these cells, which persist at a low frequency long after recovery from an acute viral infection, suggests that they play a role in protective immunological memory.
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spelling oxford-uuid:44005c81-7182-4f11-ac0c-b11c1a28b25a2022-03-26T14:59:01ZRapid effector function in CD8+ memory T cells.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:44005c81-7182-4f11-ac0c-b11c1a28b25aEnglishSymplectic Elements at Oxford1997Lalvani, ABrookes, RHambleton, SBritton, WHill, AMcMichael, AThe nature of the CD8+ T cells that underlie antiviral protective immunological memory in vivo is unclear. We have characterized peptide-specific CD8+ T lymphocytes directly ex vivo from peripheral blood in humans with past exposure to influenza virus, using single cell interferon gamma (IFN-gamma) release as a measure of effector function. In individuals in the memory state with respect to influenza virus infection, unrestimulated antigen-specific CD8+ T cells displayed IFN-gamma release within 6 h of antigen contact, identifying a population of memory CD8+ T cells that exhibit effector function without needing to divide and differentiate over several days. We have quantified circulating CD8+ effector T cells specific for six different MHC class I-restricted influenza virus epitopes. Enumeration of these CD8+ T cells gives frequencies of peptide-specific T cells that correlate with, but are in general severalfold higher than, CTL precursor frequencies derived from limiting dilution analysis, indicating that this novel population of memory CD8+ T cells has hitherto been undetected by standard means. The phenotype of these cells, which persist at a low frequency long after recovery from an acute viral infection, suggests that they play a role in protective immunological memory.
spellingShingle Lalvani, A
Brookes, R
Hambleton, S
Britton, W
Hill, A
McMichael, A
Rapid effector function in CD8+ memory T cells.
title Rapid effector function in CD8+ memory T cells.
title_full Rapid effector function in CD8+ memory T cells.
title_fullStr Rapid effector function in CD8+ memory T cells.
title_full_unstemmed Rapid effector function in CD8+ memory T cells.
title_short Rapid effector function in CD8+ memory T cells.
title_sort rapid effector function in cd8 memory t cells
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