Janssen Edith M, Lemmens Edward E, Wolfe Tom, Christen Urs, von Herrath Matthias G, Schoenberger Stephen P
Division of Cellular Immunology and Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, California 92121, USA.
Nature. 2003 Feb 20;421(6925):852-6. doi: 10.1038/nature01441. Epub 2003 Feb 9.
A long-standing paradox in cellular immunology concerns the conditional requirement for CD4+ T-helper (T(H)) cells in the priming of cytotoxic CD8+ T lymphocyte (CTL) responses in vivo. Whereas CTL responses against certain viruses can be primed in the absence of CD4+ T cells, others, such as those mediated through 'cross-priming' by host antigen-presenting cells, are dependent on T(H) cells. A clearer understanding of the contribution of T(H) cells to CTL development has been hampered by the fact that most T(H)-independent responses have been demonstrated ex vivo as primary cytotoxic effectors, whereas T(H)-dependent responses generally require secondary in vitro re-stimulation for their detection. Here, we have monitored the primary and secondary responses of T(H)-dependent and T(H)-independent CTLs and find in both cases that CD4+ T cells are dispensable for primary expansion of CD8+ T cells and their differentiation into cytotoxic effectors. However, secondary CTL expansion (that is, a secondary response upon re-encounter with antigen) is wholly dependent on the presence of T(H) cells during, but not after, priming. Our results demonstrate that T-cell help is 'programmed' into CD8+ T cells during priming, conferring on these cells a hallmark of immune response memory: the capacity for functional expansion on re-encounter with antigen.
细胞免疫学中一个长期存在的悖论涉及到在体内启动细胞毒性CD8 + T淋巴细胞(CTL)反应时对CD4 +辅助性T细胞(T(H))的条件性需求。虽然针对某些病毒的CTL反应可以在没有CD4 + T细胞的情况下启动,但其他反应,如通过宿主抗原呈递细胞的“交叉启动”介导的反应,则依赖于T(H)细胞。由于大多数不依赖T(H)的反应已在体外作为主要细胞毒性效应器得到证实,而依赖T(H)的反应通常需要在体外进行二次再刺激才能检测到,因此对T(H)细胞在CTL发育中的作用的更清晰理解受到了阻碍。在这里,我们监测了依赖T(H)和不依赖T(H)的CTL的初次和二次反应,发现在这两种情况下,CD4 + T细胞对于CD8 + T细胞的初次扩增及其分化为细胞毒性效应器都是可有可无的。然而,CTL的二次扩增(即再次遇到抗原时的二次反应)完全依赖于在启动过程中(而非启动后)T(H)细胞的存在。我们的结果表明,在启动过程中,T细胞辅助被“编程”到CD8 + T细胞中,赋予这些细胞免疫反应记忆的一个标志:再次遇到抗原时进行功能性扩增的能力。