Abstract
Although primary CD8 responses to acute infections are independent of CD4 help, it is unknown whether a similar situation applies to secondary responses. We show that depletion of CD4 cells during the recall response has minimal effect, whereas depletion during the priming phase leads to reduced responses by memory CD8 cells to reinfection. Memory CD8 cells generated in CD4+/+ mice responded normally when transferred into CD4-/- hosts, whereas memory CD8 cells generated in CD4-/- mice mounted defective recall responses in CD4+/+ adoptive hosts. These results demonstrate a previously undescribed role for CD4 help in the development of functional CD8 memory.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adoptive Transfer
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Animals
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Arenaviridae Infections / immunology
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CD8-Positive T-Lymphocytes / immunology*
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CD8-Positive T-Lymphocytes / physiology
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CD8-Positive T-Lymphocytes / transplantation
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Cell Division
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Immunization
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Immunization, Secondary
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Immunologic Memory*
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Listeria monocytogenes / genetics
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Listeria monocytogenes / immunology
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Listeriosis / immunology
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Lymphocyte Activation
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Lymphocyte Count
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Lymphocytic choriomeningitis virus / genetics
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Lymphocytic choriomeningitis virus / immunology
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Mice
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Mice, Inbred C57BL
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Mice, Inbred Strains
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Recombinant Proteins
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Spleen / cytology
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Spleen / immunology
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T-Lymphocyte Subsets / immunology
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T-Lymphocyte Subsets / physiology
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T-Lymphocytes, Helper-Inducer / immunology*