Achour A, Begue B, Gomard E, Paul P, Sayagh B, Van Pel A, Levy J P
Eur J Immunol. 1986 Jun;16(6):597-604. doi: 10.1002/eji.1830160603.
The lysis by human and murine anti-HLA cytolytic T lymphocytes (CTL) of murine cells expressing class I HLA molecule after gene transfection has been studied using two different murine cells: LMTK- and P815-HTR-TK-. Weak but significant HLA-A11-specific lysis was found occasionally with human CTL on the HLA-A11+ L cells. On the contrary, P815-A11 or P815-A2 cells were lysed strongly and specifically by HLA-A11 or HLA-A2-specific human CTL. The T8+T4- phenotype of the effector cells was confirmed and the reaction was inhibited by anti-HLA class I monoclonal antibodies. Despite their higher sensitivity to human CTL, the P815-HLA+ cells did not express higher levels of HLA antigens than L cells, and the presence or the absence of human beta 2 microglobulin was irrelevant. Anti-human LFA-1 antibodies abrogated the lysis of P815-A11+ cells showing that the LFA-1 receptor which is apparently lacking on the L cell surface was on the contrary expressed on P815 cells. On the other hand, murine anti-HLA CTL have been prepared by immunizing mice against syngeneic HLA-A11+ L cells. They lysed very efficiently and specifically these cells, but appeared completely devoid of activity against human HLA-A11 target cells. This barrier was apparently due to the H-2 restriction of these H-2k anti-HLA murine CTL, as shown by their inability to lyse allogeneic H-2d cells expressing HLA-A11, and by the blocking of their activity by anti H-2k antibodies. By contrast, xenogeneic anti-HLA CTL obtained by immunizing murine lymphocytes against human cells lysed both human and murine HLA+ cells but they reacted with a monomorphic epitope of the HLA molecule in a nonrestricted way. These results show that human cells lyse very efficiently P815 murine cells expressing HLA class I antigens; the higher sensitivity of P815 cells compared to L cells is probably due to the presence of a LFA-1 receptor on these cells; a class I molecule of human origin can be seen as an H-2-restricted minor histocompatibility antigen in another species.
利用两种不同的鼠细胞(LMTK -和P815 - HTR - TK -),研究了基因转染后表达I类HLA分子的鼠细胞被人和鼠抗HLA细胞毒性T淋巴细胞(CTL)裂解的情况。偶尔发现人CTL对HLA - A11 + L细胞有微弱但显著的HLA - A11特异性裂解。相反,HLA - A11或HLA - A2特异性人CTL能强烈且特异性地裂解P815 - A11或P815 - A2细胞。证实了效应细胞的T8 + T4 -表型,且该反应被抗I类HLA单克隆抗体抑制。尽管P815 - HLA +细胞对人CTL的敏感性更高,但它们表达的HLA抗原水平并不比L细胞高,人β2微球蛋白的存在与否无关紧要。抗人LFA - 1抗体消除了对P815 - A11 +细胞的裂解,表明L细胞表面明显缺乏的LFA - 1受体在P815细胞上表达。另一方面,通过用同基因HLA - A11 + L细胞免疫小鼠制备了鼠抗HLA CTL。它们能非常有效地且特异性地裂解这些细胞,但对人HLA - A11靶细胞似乎完全没有活性。这种障碍显然是由于这些H - 2k抗HLA鼠CTL的H - 2限制,这可通过它们不能裂解表达HLA - A11的同种异体H - 2d细胞以及抗H - 2k抗体对其活性的阻断来证明。相比之下,通过用鼠淋巴细胞免疫人细胞获得的异种抗HLA CTL能裂解人和鼠的HLA +细胞,但它们以非限制性方式与HLA分子的一个单态表位反应。这些结果表明,人细胞能非常有效地裂解表达I类HLA抗原的P815鼠细胞;P815细胞比L细胞更高的敏感性可能是由于这些细胞上存在LFA - 1受体;源自人的I类分子在另一个物种中可被视为一种受H - 2限制的次要组织相容性抗原。