Most microbe-specific naïve CD4 + T cells produce memory cells during infection
Author(s) -
Noah J. Tubo,
Brian T. Fife,
Antonio J. Pagán,
Dmitri I. Kotov,
Michael F. Goldberg,
Marc K. Jenkins
Publication year - 2016
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aad0483
Subject(s) - adoptive cell transfer , biology , immune system , effector , population , memory t cell , immunology , cell , spleen , t cell , b 1 cell , memory cell , microbiology and biotechnology , antigen presenting cell , genetics , medicine , physics , transistor , quantum mechanics , voltage , environmental health
Infection elicits CD4(+) memory T lymphocytes that participate in protective immunity. Although memory cells are the progeny of naïve T cells, it is unclear that all naïve cells from a polyclonal repertoire have memory cell potential. Using a single-cell adoptive transfer and spleen biopsy method, we found that in mice, essentially all microbe-specific naïve cells produced memory cells during infection. Different clonal memory cell populations had different B cell or macrophage helper compositions that matched effector cell populations generated much earlier in the response. Thus, each microbe-specific naïve CD4(+) T cell produces a distinctive ratio of effector cell types early in the immune response that is maintained as some cells in the clonal population become memory cells.
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