CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes

A long-standing paradox in cellular immunology concerns the conditional requirement for CD4 + T-helper (T H ) cells in the priming of cytotoxic CD8 + T lymphocyte (CTL) responses in vivo . Whereas CTL responses against certain viruses can be primed in the absence of CD4 + T cells, others, such as th...

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Veröffentlicht in:Nature (London) 2003-02, Vol.421 (6925), p.852-856
Hauptverfasser: Janssen, Edith M., Lemmens, Edward E., Wolfe, Tom, Christen, Urs, von Herrath, Matthias G., Schoenberger, Stephen P.
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container_title Nature (London)
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creator Janssen, Edith M.
Lemmens, Edward E.
Wolfe, Tom
Christen, Urs
von Herrath, Matthias G.
Schoenberger, Stephen P.
description A long-standing paradox in cellular immunology concerns the conditional requirement for CD4 + T-helper (T H ) cells in the priming of cytotoxic CD8 + T lymphocyte (CTL) responses in vivo . Whereas CTL responses against certain viruses can be primed in the absence of CD4 + T cells, others, such as those mediated through ‘cross-priming’ by host antigen-presenting cells, are dependent on T H cells 1 , 2 , 3 , 4 . A clearer understanding of the contribution of T H cells to CTL development has been hampered by the fact that most T H -independent responses have been demonstrated ex vivo as primary cytotoxic effectors, whereas T H -dependent responses generally require secondary in vitro re-stimulation for their detection. Here, we have monitored the primary and secondary responses of T H -dependent and T H -independent CTLs and find in both cases that CD4 + T cells are dispensable for primary expansion of CD8 + T cells and their differentiation into cytotoxic effectors. However, secondary CTL expansion (that is, a secondary response upon re-encounter with antigen) is wholly dependent on the presence of T H cells during, but not after, priming. Our results demonstrate that T-cell help is ‘programmed’ into CD8 + T cells during priming, conferring on these cells a hallmark of immune response memory: the capacity for functional expansion on re-encounter with antigen.
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source MEDLINE; Nature; SpringerLink Journals - AutoHoldings
subjects Animals
Antigens - immunology
Biological and medical sciences
Cell Line
Cellular biology
Cytotoxicity, Immunologic
Flow Cytometry
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humanities and Social Sciences
Immune response
Immunobiology
Immunologic Memory
Immunology
letter
Lymphocyte Activation
Lymphocytes
Lymphocytic choriomeningitis virus - immunology
Lymphoid cells: ontogeny, maturation, markers, receptors, circulation and recirculation
Mice
multidisciplinary
Science
Science (multidisciplinary)
T-Lymphocytes, Cytotoxic - cytology
T-Lymphocytes, Cytotoxic - immunology
T-Lymphocytes, Helper-Inducer - immunology
title CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes
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