Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Cold Spring Harb Perspect Med. 2013 Dec 1;3(12):a015537. doi: 10.1101/cshperspect.a015537.
Before it became possible to derive T-cell lines and clones, initial experimentation on the activation requirements of T lymphocytes was performed on transformed cell lines, such as Jurkat. These studies, although technically correct, proved misleading as most transformed T cells can be activated by stimulation of the clonotypic T-cell receptor (TCR) alone. In contrast, once it became possible to study nontransformed T cells, it quickly became clear that TCR stimulation by itself is insufficient for optimal activation of naïve T cells, but in fact, induces a state of anergy. It then became clear that functional activation of T cells requires not only recognition of major histocompatibility complex (MHC) and peptide by the TCR, but also requires ligation of costimulatory receptors expressed on the cell surface.
在能够获得 T 细胞系和克隆之前,人们最初在转化细胞系(如 Jurkat)上进行了 T 淋巴细胞激活要求的实验。这些研究虽然在技术上是正确的,但证明是有误导性的,因为大多数转化的 T 细胞可以通过单独刺激克隆型 T 细胞受体(TCR)来激活。相比之下,一旦有可能研究未转化的 T 细胞,就很快清楚地表明,TCR 刺激本身不足以使幼稚 T 细胞最佳激活,实际上会诱导无反应状态。然后很明显,T 细胞的功能激活不仅需要 TCR 识别主要组织相容性复合物(MHC)和肽,还需要细胞表面表达的共刺激受体的连接。