Letvin N L, Kauffman R S, Finberg R
J Immunol. 1981 Dec;127(6):2334-9.
The cellular requirements for the development of an immune response to reovirus type 1 and the role of such a response in the clearance of a primary infection with that virus were explored. An Ia-bearing antigen-presenting cell requirement is demonstrated for the in vitro generation of secondary anti-reovirus cytolytic T lymphocytes (CTL). It is then shown that mice whose spleens are depleted of Ia-bearing adherent cells by exposure in vivo to ultraviolet (UV) radiation exhibit depressed priming for reovirus-specific T lymphocyte function-CTL generation, delayed-type hypersensitivity reactivity, and T cell proliferative responsiveness. These UV-irradiated mice clear primary systemic reovirus infections as readily as normal mice. Further, athymic 'nude' mice show no defect in their ability to clear a reovirus infection. The implications of these findings for our understanding of the role of virus-specific T cell function in the clearance of systemic viral infections are discussed.
探讨了对1型呼肠孤病毒产生免疫反应的细胞需求以及这种反应在清除该病毒原发性感染中的作用。已证明,体外产生继发性抗呼肠孤病毒细胞毒性T淋巴细胞(CTL)需要Ia阳性抗原呈递细胞。随后表明,通过体内暴露于紫外线(UV)辐射而使脾脏中Ia阳性黏附细胞耗竭的小鼠,对呼肠孤病毒特异性T淋巴细胞功能(CTL产生)的启动受到抑制,迟发型超敏反应性降低,T细胞增殖反应性降低。这些经紫外线照射的小鼠清除原发性全身性呼肠孤病毒感染的速度与正常小鼠一样快。此外,无胸腺“裸”鼠在清除呼肠孤病毒感染的能力上没有缺陷。讨论了这些发现对于我们理解病毒特异性T细胞功能在全身性病毒感染清除中的作用的意义。