Ashton-Rickardta P G, Opferman J T
Committee on Immunology, Gwen Knapp Center for Lupus and Immunology Research, The University of Chicago, Illinois 60637-5420, USA.
Cell Mol Life Sci. 1999 Oct 1;56(1-2):69-77. doi: 10.1007/s000180050007.
Immunological memory protects organisms from recurrent challenge by pathogens. The persistence of a heightened reactive state initiated by antigenic challenge is mediated by long-lived memory lymphocytes. The survival of memory T cells is thought to require stimulation through the T cell receptor (TCR), sometimes by persistent antigen. However, memory T cells can survive in the absence of antigen, in which case TCR stimulation provided by cell surface self-peptide/ major histocompatibility complex (MHC) molecules and cytokines are required to sustain memory T cells. Recent work using mouse models has provided insights into the origin of memory T cells. Understanding the mechanisms that underlie the differentiation and persistence of memory T cells may improve the effectiveness of vaccines through the induction of T cell memory.
免疫记忆可保护生物体免受病原体的反复攻击。由抗原刺激引发的高反应性状态的持续存在是由长寿记忆淋巴细胞介导的。记忆T细胞的存活被认为需要通过T细胞受体(TCR)进行刺激,有时是由持续性抗原刺激。然而,记忆T细胞在没有抗原的情况下也能存活,在这种情况下,细胞表面自身肽/主要组织相容性复合体(MHC)分子和细胞因子提供的TCR刺激是维持记忆T细胞所必需的。最近使用小鼠模型开展的研究为记忆T细胞的起源提供了深入见解。了解记忆T细胞分化和持续存在的机制可能会通过诱导T细胞记忆来提高疫苗的有效性。