Okazaki K, Morita M, Nishimori I, Sano S, Toyonaga M, Nakazawa Y, Yamamoto Y, Yamamoto Y
First Department of Internal Medicine, Kochi Medical School, Japan.
Gastroenterology. 1993 Feb;104(2):384-91. doi: 10.1016/0016-5085(93)90405-2.
The role of cytotoxicity mediated by peripheral blood mononuclear cells for colonic epithelial cells in inflammatory bowel disease (IBD) is still controversial. To clarify it, we studied major histocompatibility antigen (MHC)-restricted T cell-mediated cytotoxicity (CTL).
Cytotoxicity was measured by 51Cr release from colonic cells after the 6-hour incubation with peripheral blood mononuclear cells in 11 IBD patients (6 with Crohn's disease and 5 with ulcerative colitis).
CTL activity (E/T ratio = 200:1 or 100:1) for autologous target cells was significantly increased (22%-40%) in 5 of 6 CD and 4 of 5 UC patients (22%-64%) compared with that for allogeneic target cells. The increase in CTL activity was mainly inhibited by anti-MHC class I and CD8 monoclonal antibodies (50 micrograms/mL), while it was partially inhibited by anti-MHC class II or CD4 antibodies in some patients. Complement-mediated depletion of CD2+ cells also significantly decreased CTL activity.
The results indicate that MHC-restricted T cell cytotoxicity may play a role in mucosal damage in some patients of IBD.
外周血单核细胞介导的细胞毒性作用在炎症性肠病(IBD)中对结肠上皮细胞的作用仍存在争议。为阐明这一点,我们研究了主要组织相容性抗原(MHC)限制的T细胞介导的细胞毒性(CTL)。
在11例IBD患者(6例克罗恩病患者和5例溃疡性结肠炎患者)中,将外周血单核细胞与结肠细胞孵育6小时后,通过51Cr释放来测定细胞毒性。
与异体靶细胞相比,6例CD患者中的5例以及5例UC患者中的4例(22%-64%)对自体靶细胞的CTL活性(效靶比=200:1或100:1)显著增加(22%-40%)。CTL活性的增加主要受到抗MHC I类和CD8单克隆抗体(50微克/毫升)的抑制,而在一些患者中,抗MHC II类或CD4抗体可部分抑制该活性。补体介导的CD2+细胞耗竭也显著降低了CTL活性。
结果表明,MHC限制的T细胞细胞毒性可能在部分IBD患者的黏膜损伤中起作用。