Gumperz J E, Litwin V, Phillips J H, Lanier L L, Parham P
Department of Microbiology & Immunology, Stanford University, California 94305.
J Exp Med. 1995 Mar 1;181(3):1133-44. doi: 10.1084/jem.181.3.1133.
Although inhibition of natural killer (NK) cell-mediated lysis by the class I HLA molecules of target cells is an established phenomenon, knowledge of the features of class I molecules which induce this effect remains rudimentary. Using class I alleles HLA-B1502 and B1513 which differ only at residues 77-83 which define the Bw4 and Bw6 serological epitopes, we tested the hypothesis that the presence of the Bw4 epitope on class I molecules determines recognition by NKB1+ NK cells. HLA-B1513 possesses the Bw4 epitope, whereas B1502 has the Bw6 epitope. Lysis by NKB1+ NK cell clones of transfected target cells expressing B1513 as the only HLA-A, -B, or -C molecule was inhibited, whereas killing of transfectants expressing B1502 was not. Addition of an an anti-NKB1 monoclonal antibody reconstituted lysis of the targets expressing B1513, but did not affect killing of targets bearing B1502. The inhibitory effect of B1513 could be similarly prevented by the addition of an anti-class I monoclonal antibody. These results show that the presence of the Bw4 epitope influences recognition of HLA-B molecules by NK cells that express NKB1, and suggest that the NKB1 molecule may act as a receptor for Bw4+ HLA-B alleles. Sequences outside of the Bw4 region must also affect recognition by NKB1+ NK cells, because lysis of transfectants expressing HLA-A2403 or A2501, which possess the Bw4 epitope but are in other ways substantially different from HLA-B molecules, was not increased by addition of the anti-NKB1 antibody. Asparagine 86, the single site of N-linked glycosylation on class I molecules, is in close proximity to the Bw4/Bw6 region. The glycosylation site of the Bw4-positive molecule B5801 was mutated, and the mutant molecules tested for inhibition of NKB1+ NK cells. Inhibition that could be reversed by addition of the anti-NKB1 monoclonal antibody was observed, showing the presence of the carbohydrate moiety is not essential for class I recognition by NKB1+ NK cell clones.
尽管靶细胞的I类HLA分子对自然杀伤(NK)细胞介导的细胞溶解作用的抑制是一个既定现象,但对于诱导这种效应的I类分子特征的了解仍然很基础。利用仅在定义Bw4和Bw6血清学表位的第77 - 83位残基上不同的I类等位基因HLA - B1502和B1513,我们检验了I类分子上Bw4表位的存在决定NKB1⁺ NK细胞识别的假说。HLA - B1513具有Bw4表位,而B1502具有Bw6表位。表达B1513作为唯一HLA - A、- B或- C分子的转染靶细胞被NKB1⁺ NK细胞克隆溶解的作用受到抑制,而表达B1502的转染细胞的杀伤作用则未受影响。添加抗NKB1单克隆抗体可恢复对表达B1513的靶细胞的溶解作用,但不影响对携带B1502的靶细胞的杀伤。添加抗I类单克隆抗体同样可以阻止B1513的抑制作用。这些结果表明Bw4表位的存在影响表达NKB1的NK细胞对HLA - B分子的识别,并提示NKB1分子可能作为Bw4⁺ HLA - B等位基因的受体。Bw4区域之外的序列也必定影响NKB1⁺ NK细胞的识别,因为表达HLA - A2403或A2501(它们具有Bw4表位但在其他方面与HLA - B分子有很大不同)的转染细胞,添加抗NKB1抗体后其溶解作用并未增强。I类分子上N - 连接糖基化的唯一位点天冬酰胺86紧邻Bw4/Bw6区域。对Bw4阳性分子B5801的糖基化位点进行突变,并检测突变分子对NKB1⁺ NK细胞的抑制作用。观察到添加抗NKB1单克隆抗体可逆转的抑制作用,表明碳水化合物部分对于NKB1⁺ NK细胞克隆识别I类分子并非必不可少。