Biddison W E, Hansen T H, Levy R B, Doherty P C
J Exp Med. 1978 Dec 1;148(6):1678-86. doi: 10.1084/jem.148.6.1678.
The H-2L locus is closely linked to H-2D and codes for antigenic specificities present on a 45,000 mol wt glycoprotein that is distinct from the molecule which bears the D region private specificity. It was found that BALB/c-H-2db mice, which lack detectable cell-surface H-2L gene products, were able to generate influenza- and vaccinia-immune cytotoxic T cells which lyse D region-compatible target cells, although they have been reported to be incapable of making a similar response to ectromelia virus (7). Thus, the lack of H-2L antigenic specificities does not produce a general loss of responsiveness for other viruses even when a highly cross-reactive pox virus (vaccinia) was studied. Antisera-blocking experiments utilizing sera specific for either L or D molecules indicated that BALB/c mice generate influenza virus-immune cytotoxic T-cell subsets which independently recognize H-2L and H-2D gene products in association with viral antigens. These results are the first indication that products of the H-2L locus can operate analogously to H-2K/D gene products in virus-immune T-cell recognition.
H-2L基因座与H-2D紧密连锁,编码一种45,000分子量糖蛋白上存在的抗原特异性,该糖蛋白与携带D区私有特异性的分子不同。已发现缺乏可检测到的细胞表面H-2L基因产物的BALB/c-H-2db小鼠能够产生流感和痘苗免疫细胞毒性T细胞,这些细胞可裂解D区相容的靶细胞,尽管据报道它们对埃可病毒无类似反应(7)。因此,即使研究的是高度交叉反应的痘病毒(痘苗),缺乏H-2L抗原特异性也不会导致对其他病毒的反应性普遍丧失。利用针对L或D分子的特异性血清进行的抗血清阻断实验表明,BALB/c小鼠产生流感病毒免疫细胞毒性T细胞亚群,它们独立识别与病毒抗原相关的H-2L和H-2D基因产物。这些结果首次表明,H-2L基因座的产物在病毒免疫T细胞识别中可与H-2K/D基因产物类似地发挥作用。