Reinherz E L, Schlossman S F
Division of Tumor Immunology, Sidney Farber Cancer Institute and the Department of Medicine, Harvard Medical School, Boston, MA 02115, U.S.A.
Immunol Today. 1981 Apr;2(4):69-75. doi: 10.1016/0167-5699(81)90019-0.
Functional T lymphocyte subpopulations can be identified in humans by antibodies which detect stable glycoprotein antigens on their surface. Thus, inducer T lymphocytes bear an antigen termed T4 while suppressor T lymphocytes bear an antigen termed T5. Immune homeostasis results from a delicate balance between inducer and suppressor subsets within the T-cell circuit and perturbation in subset dynamics may initiate a wide variety of immunopathological disorders. Here Ellis Reinherz and Stuart Schlossman discuss the present understanding of this circuit, its role in the pathogenesis of a number of diseases and how the human immune response can be manipulated in an orderly way through modulation of selected T-cell subsets.
功能性T淋巴细胞亚群可通过检测其表面稳定糖蛋白抗原的抗体在人类中得以识别。因此,诱导性T淋巴细胞带有一种名为T4的抗原,而抑制性T淋巴细胞带有一种名为T5的抗原。免疫稳态源于T细胞回路中诱导性和抑制性亚群之间的微妙平衡,亚群动态的扰动可能引发多种免疫病理疾病。在此,埃利斯·赖因赫兹和斯图尔特·施洛斯曼讨论了目前对该回路的理解、其在多种疾病发病机制中的作用,以及如何通过调节选定的T细胞亚群以有序的方式操控人类免疫反应。