Mingari M C, Ponte M, Vitale C, Bellomo R, Moretta L
Istituto Nazionale per la Ricerca sul Cancro, Dipartimento di Oncologia, Biologia e Genetica, University of Genova, Italy.
Hum Immunol. 2000 Jan;61(1):44-50. doi: 10.1016/s0198-8859(99)00158-5.
Different families of major histocompatibility complex (MHC)-specific inhibitory receptors (NKRs) play a major role in natural killer (NK) cell function, allowing discrimination between normal cells and cells that do not express adequate amounts of MHC class I antigens. This occurs in most instances as a consequence of viral infection or tumor transformation. In T lymphocytes, expression of NKR is mostly confined to activated CD8+ cytolytic T lymphocytes (CTLs). While NKR expression by CTLs may be viewed as a mechanism preventing damages to normal cells by those CTLs that have acquired NK-like activity, it may also down regulate TCR-mediated T cell activation, thus, impairing CTL functions. The finding that certain cytokines can modulate killer inhibitory receptor expression in CTLs is of major interest and might be instrumental in novel therapeutic approaches aimed at the down regulation ofT-cell function in transplantation or autoimmunity.
不同家族的主要组织相容性复合体(MHC)特异性抑制性受体(NKRs)在自然杀伤(NK)细胞功能中起主要作用,使NK细胞能够区分正常细胞和不表达足够量MHC I类抗原的细胞。在大多数情况下,这是病毒感染或肿瘤转化的结果。在T淋巴细胞中,NKR的表达大多局限于活化的CD8 + 细胞毒性T淋巴细胞(CTLs)。虽然CTLs表达NKR可被视为一种机制,防止具有NK样活性的CTLs对正常细胞造成损害,但它也可能下调TCR介导的T细胞活化,从而损害CTL功能。某些细胞因子可调节CTLs中杀伤抑制受体表达这一发现具有重要意义,可能有助于开发旨在下调移植或自身免疫中T细胞功能的新型治疗方法。