Kassiotis George, Garcia Sylvie, Simpson Elizabeth, Stockinger Brigitta
Division of Molecular Immunology, The National Institute for Medical Research, Mill Hill, London NW7 1AA, UK.
Nat Immunol. 2002 Mar;3(3):244-50. doi: 10.1038/ni766. Epub 2002 Feb 11.
The mechanisms by which immunological memory is maintained after infection or vaccination are still a matter of debate. Long-term survival of memory T cells does not require major histocompatibility complex (MHC) contact. We show here that compared with memory CD4+ T cells that maintain contact with MHC class II, memory CD4+ T cells deprived of MHC class II contact show distinct functional defects upon antigen re-encounter. Thus, in contrast to their survival, maintenance of the typical quality of memory T cells crucially depends on MHC-derived signals.
感染或接种疫苗后免疫记忆得以维持的机制仍是一个有争议的问题。记忆T细胞的长期存活并不需要与主要组织相容性复合体(MHC)接触。我们在此表明,与维持与II类MHC接触的记忆CD4+ T细胞相比,被剥夺II类MHC接触的记忆CD4+ T细胞在再次遇到抗原时表现出明显的功能缺陷。因此,与它们的存活情况相反,记忆T细胞典型特性的维持关键取决于MHC衍生的信号。