Botzenhardt U, Müller-Quernheim J
I. Medizinische Klinik, Johannes Gutenberg Universität, Mainz, FRG.
Clin Exp Immunol. 1987 Sep;69(3):647-51.
NZB-mice have a T cell hyperreactivity based on a primary response to minor histocompatibility antigens (MIH) on target cells identical to NZB on the H-2 complex (MHC). We tested the idea that a single MIH difference on MHC identical target cells is sufficient to elicit such a primary response in vitro. Cytotoxic T lymphocyte (CTL) response and activated T-helper cell (THC) frequencies were evaluated. NZB x CBA/J (Mls a/d) and NZB x CBA/Ca (Mls a/b) hybrids, which differ only at the M-locus, were raised. A primary cytotoxic response in the direction Mls b anti Mls d, but not vice versa was observed in vitro. In the assay used no unusual THC frequencies against Mls d could be demonstrated. The results favour cellular hyperreactivity in NZB which can be elicited by a single MIH antigen alone.
NZB小鼠对与H-2复合体(主要组织相容性复合体,MHC)上的NZB相同的靶细胞上的次要组织相容性抗原(MIH)存在基于初次反应的T细胞反应过度。我们测试了这样一种观点,即在MHC相同的靶细胞上单个MIH差异足以在体外引发这种初次反应。评估了细胞毒性T淋巴细胞(CTL)反应和活化的T辅助细胞(THC)频率。培育了仅在M位点不同的NZB×CBA/J(Mls a/d)和NZB×CBA/Ca(Mls a/b)杂种。在体外观察到了Mls b抗Mls d方向的初次细胞毒性反应,但反之则未观察到。在所使用的检测方法中,未证明对Mls d存在异常的THC频率。结果支持NZB中细胞反应过度,这可由单一的MIH抗原单独引发。