Wölpl A, Halder T, Kalbacher H, Neumeyer H, Siemoneit K, Goldmann S F, Eiermann T H
Department of Transfusion Medicine, University of Ulm, Red Cross Blood Bank Ulm, Germany.
Tissue Antigens. 1998 Mar;51(3):258-69. doi: 10.1111/j.1399-0039.1998.tb03100.x.
Alloreactive T cells recognize peptides presented in the binding groove of major histocompatibility complex molecules (MHCs), whereas B cells mainly recognize the MHCs independent of bound peptides. Here, we demonstrate that the human B-cell repertoire comprises B cells which can be stimulated during pregnancy to produce antibodies reacting with MHCs in a way similar to T cells. The human monoclonal antibody UL-5A1 recognizes DR1(DRA/DRB1*0101) molecules on lymphoblastoid cell lines only if they co-express HLA-A2 or if they have been loaded with HLA-A2-derived peptides. The effect of the HLA-A2 peptide 105-117 on UL-5A1 reactivity was specific, time and dose-dependent. Reactivity increased when naturally processed peptides were removed from DR1 molecules before the HLA-A2 peptide 105-117 was loaded. UL-5A1 reacted specifically with cells that had been activated. The results imply a role of activation of cells in peptide processing and/or loading.
同种异体反应性T细胞识别主要组织相容性复合体分子(MHC)结合槽中呈递的肽段,而B细胞主要识别独立于结合肽段的MHC。在此,我们证明人类B细胞库包含在妊娠期间可被刺激产生以类似于T细胞的方式与MHC反应的抗体的B细胞。人单克隆抗体UL-5A1仅在淋巴母细胞系共表达HLA-A2或已加载HLA-A2衍生肽段时才识别其上的DR1(DRA/DRB1*0101)分子。HLA-A2肽段105-117对UL-5A1反应性的影响具有特异性、时间依赖性和剂量依赖性。在加载HLA-A2肽段105-117之前从DR1分子中去除天然加工的肽段时,反应性增加。UL-5A1与已被激活的细胞特异性反应。结果表明细胞激活在肽段加工和/或加载中起作用。