Halliday G M, Odling K A, Muller H K
Department of Dermatology, University of Sydney, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Cell Immunol. 1993 Oct 15;151(2):291-9. doi: 10.1006/cimm.1993.1239.
Treatment of skin with the chemical carcinogen 7,12-dimethylbenz[a]anthracene (DMBA), which reduces the density of epidermal class II MHC-expressing Langerhans cells (LC), enhances its survival when transplanted onto histoincompatible hosts. We have examined the ability of T lymphocytes which reject DMBA-treated skin to lyse P388D1 cells expressing either only class I or class I and II antigens. Lymphocytes isolated from solvent-treated grafts showed greater cytotoxicity for the targets expressing both antigens, indicating that some of these lymphocytes were specific for class II MHC antigens. In contrast, lymphocytes isolated from carcinogen-treated grafts lysed both targets similarly and hence did not contain any cells specific for class II MHC antigens. Anti-class I MHC antibody blocked cytotoxicity by both leukocyte populations to similar extents, but anti-class II MHC antibodies preferentially blocked T cells isolated from the solvent-treated grafts. There was no difference in the phenotype of the cytotoxic cells isolated from solvent- and carcinogen-treated grafts. Thus, whereas solvent-treated skin grafts are rejected by T cells specific for class I and II MHC antigens, DMBA-treated skin grafts are only rejected by class I MHC-specific T cells which may account for the enhanced survival of the carcinogen-treated grafts.
用化学致癌物7,12 - 二甲基苯并[a]蒽(DMBA)处理皮肤,会降低表达表皮II类主要组织相容性复合体(MHC)的朗格汉斯细胞(LC)的密度,而当将其移植到组织不相容的宿主上时,却能提高其存活率。我们检测了排斥经DMBA处理皮肤的T淋巴细胞裂解仅表达I类或同时表达I类和II类抗原的P388D1细胞的能力。从经溶剂处理的移植物中分离出的淋巴细胞对表达两种抗原的靶细胞表现出更强的细胞毒性,这表明这些淋巴细胞中的一些对II类MHC抗原具有特异性。相比之下,从经致癌物处理的移植物中分离出的淋巴细胞对两种靶细胞的裂解作用相似,因此不含有任何对II类MHC抗原具有特异性的细胞。抗I类MHC抗体对两种白细胞群体的细胞毒性的阻断程度相似,但抗II类MHC抗体优先阻断从经溶剂处理的移植物中分离出的T细胞。从经溶剂处理和经致癌物处理的移植物中分离出的细胞毒性细胞的表型没有差异。因此,虽然经溶剂处理的皮肤移植物被对I类和II类MHC抗原具有特异性的T细胞排斥,但经DMBA处理的皮肤移植物仅被对I类MHC具有特异性的T细胞排斥,这可能解释了经致癌物处理的移植物存活率提高的原因。