4.7 Article

CD4+ T cells are required for the maintenance, not programming, of memory CD8+ T cells after acute infection

Journal

NATURE IMMUNOLOGY
Volume 5, Issue 9, Pages 927-933

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ni1105

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Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NCI NIH HHS [CA09537, T32 CA009537] Funding Source: Medline
  3. NIAID NIH HHS [AI056809, R01 AI019335-19, AI19335, F32 AI056809-01, R01 AI019335, F32 AI056809] Funding Source: Medline

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Immunization in the absence of CD4(+) T cell help results in defective CD8(+) T cell memory, deficient recall responses and diminished protective immunity. Here we investigated at what stage during the immune response to pathogen CD4(+) T cells are essential in the promotion of functional CD8(+) T cell memory. Memory CD8(+) T cell numbers decreased gradually in the absence of CD4(+) T cells despite the presence of similar numbers of memory cell precursors at the peak of the effector phase. Adoptive transfer of effector or memory CD8(+) T cells into wild-type or CD4(+) T cell-deficient mice demonstrated that the presence of CD4(+) T cells was important only after, not during, the early CD8(+) T cell programming phase. In the absence of CD4(+) T cells, memory CD8(+) T cells became functionally impaired and decreased in quantity over time. We conclude that in the context of an acute infection, CD4(+) T cells are required only during the maintenance phase of long-lived memory CD8(+) T cells.

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