Carter L L, Swain S L
Trudeau Institute, Saranac Lake, NY 12983, USA.
Immunol Res. 1998 Aug;18(1):1-13. doi: 10.1007/BF02786509.
Specific immune responses proceed through and are regulated at several stages: activation of naive cells and their differentiation into effector cells, completion of effector functions, development of memory cells, and subsequent reactivation of memory cells. To understand the development and regulation of CD4+ T cells in immune responses, naive CD4+ T cells were enriched from T cell receptor (TCR) transgenic mice, and used to generate effector and memory populations in vivo and in vitro. The expression of a common TCR on all of these developmental subsets has allowed us to compare directly their phenotype, cytokine profiles, activation requirements, and susceptibility to apoptosis. Our experiments have revealed interesting distinctions among naive, effector, and memory subsets of CD4+ T cells and have important implications for our understanding of immune responses.
初始细胞的激活及其分化为效应细胞、效应功能的完成、记忆细胞的发育以及随后记忆细胞的再次激活。为了了解免疫反应中CD4+ T细胞的发育和调节,从T细胞受体(TCR)转基因小鼠中富集初始CD4+ T细胞,并用于在体内和体外生成效应细胞群和记忆细胞群。所有这些发育亚群上共同TCR的表达使我们能够直接比较它们的表型、细胞因子谱、激活需求以及对凋亡的敏感性。我们的实验揭示了CD4+ T细胞的初始、效应和记忆亚群之间有趣的差异,并对我们理解免疫反应具有重要意义。