Tubo Noah J, Fife Brian T, Pagan Antonio J, Kotov Dmitri I, Goldberg Michael F, Jenkins Marc K
Immune Mediated Disease Therapy Group, Genzyme, a Sanofi Company, Framingham, MA 01701, USA.
Department of Medicine, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Science. 2016 Jan 29;351(6272):511-4. doi: 10.1126/science.aad0483.
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.
感染会引发参与保护性免疫的CD4(+)记忆T淋巴细胞。虽然记忆细胞是初始T细胞的后代,但尚不清楚来自多克隆库的所有初始细胞是否都具有产生记忆细胞的潜力。通过单细胞过继转移和脾脏活检方法,我们发现,在小鼠中,基本上所有微生物特异性初始细胞在感染期间都会产生记忆细胞。不同的克隆记忆细胞群体具有不同的B细胞或巨噬细胞辅助细胞组成,这些组成与在应答中更早产生的效应细胞群体相匹配。因此,每个微生物特异性初始CD4(+) T细胞在免疫应答早期都会产生独特比例的效应细胞类型,并且随着克隆群体中的一些细胞成为记忆细胞,这种比例会得以维持。