Journal
JOURNAL OF IMMUNOLOGY
Volume 176, Issue 5, Pages 3028-3036Publisher
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.176.5.3028
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- NIAID NIH HHS [AI-52351] Funding Source: Medline
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The early events regulating antiviral CD4 responses were tracked using an adoptive transfer model. CD4(+) T cell expansion was nonlinear, with a lengthy lag phase followed by 2 days of explosive proliferation. A small number of naive Ag-specific CD4(+) T cells were found in nonlymphoid tissues and, in the 8 days following infection, the number of activated cells increased in all tissues analyzed, and their effector functions matured. Finally, we show that a naive mouse contains similar to 100 naive CD4(+) precursor cells specific for a single epitope, a precursor frequency of similar to 10(-5), similar to that of naive CD8(+) T cells, indicating that the similar to 50-fold difference in size of the two responses to virus infection is determined by something other than the number of precursor cells.
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