The University of Queensland Diamantina Institute, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
J Invest Dermatol. 2010 Jul;130(7):1841-8. doi: 10.1038/jid.2010.49. Epub 2010 Mar 18.
The immune system surveys the skin for keratinocytes (KCs) infected by viruses or with acquired genetic damage. The mechanism by which T cells mediate KC elimination is however undefined. In this study we show that antigen-specific CD8 T cells can eliminate antigen-bearing KCs in vivo and inhibit their clonogenic potential in vitro, independently of the effector molecules perforin and Fas-ligand (Fas-L). In contrast, IFN-gamma receptor expression on KCs and T cells producing IFN-gamma are each necessary and sufficient for in vitro inhibition of KC clonogenic potential. Thus, antigen-specific cytotoxic T lymphocytes (CTLs) may mediate destruction of epithelium expressing non-self antigen by eliminating KCs with potential for self-renewal through an IFN-gamma-dependent mechanism.
免疫系统会对感染病毒或获得遗传损伤的角质形成细胞 (KCs) 进行检测。然而,T 细胞介导 KC 消除的机制尚未明确。在这项研究中,我们发现抗原特异性 CD8 T 细胞可以在体内消除携带抗原的 KCs,并在体外抑制其克隆形成能力,而不依赖于效应分子穿孔素和 Fas 配体 (Fas-L)。相比之下,KCs 和产生 IFN-γ的 T 细胞上 IFN-γ受体的表达对于体外抑制 KC 克隆形成能力是必要且充分的。因此,抗原特异性细胞毒性 T 淋巴细胞 (CTL) 可能通过一种依赖 IFN-γ的机制消除具有自我更新潜力的 KCs,从而介导表达非自身抗原的上皮细胞的破坏。