Iványi D, Snoek M, Démant P
Tissue Antigens. 1979 Sep;14(3):233-50. doi: 10.1111/j.1399-0039.1979.tb00845.x.
The H-2L molecules were detected for the first time in the Dd region products using antisera against the public specificity H-2.28. This specificity was analyzed because its presence in K as well as in D region products and its apparent allelism with another public specificity, H-2.1, indicated that these two specificities may have a special position may have a special position in the H-2 system. This was corroborated by subsequent identification of H-2L molecules in Dq and Dk products using anti-H-2.28 AND ANTI-H-2.1 sera, respectively, while none of the other previously known public or private specificities was detected on H-2L molecules. We tested the products of four D region alleles which had not been analyzed previously. In each of them we identified two distinct types of molecules: H-2D, which reacts with sera agains the D region private specificity, and H-2L, which does not react with these sera, but which is detectable either by anti-H-2.28 sera (H-2Lb, H-2Lf, H-2LS) or by anti-H-2.1 sera (H-2Ldx). This increases the number of identified H-2L alleles to seven (five H-2.8+, two H-2.1+). No association between H-2D and H-2D and H-2L molecules on the cell surface was detected in capping experiments.
利用针对公共特异性H-2.28的抗血清,首次在Dd区域产物中检测到H-2L分子。对这种特异性进行分析是因为它在K区域产物以及D区域产物中都存在,并且与另一种公共特异性H-2.1明显存在等位基因关系,这表明这两种特异性在H-2系统中可能具有特殊地位。随后分别使用抗H-2.28血清和抗H-2.1血清在Dq和Dk产物中鉴定出H-2L分子,进一步证实了这一点,而在H-2L分子上未检测到其他任何先前已知的公共或私有特异性。我们检测了四个先前未分析过的D区域等位基因的产物。在每个产物中,我们鉴定出两种不同类型的分子:与针对D区域私有特异性的血清发生反应的H-2D,以及不与这些血清发生反应,但可通过抗H-2.28血清(H-2Lb、H-2Lf、H-2LS)或抗H-2.1血清(H-2Ldx)检测到的H-2L。这使得已鉴定的H-2L等位基因数量增加到七个(五个H-2.8 +,两个H-2.1 +)。在封帽实验中未检测到细胞表面H-2D和H-2L分子之间的关联。