Lardy N M, Bakas R M, van der Horst A R, van Twuyver E, Bontrop R E, de Waal L P
Department of Transplantation Immunology, Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam.
J Immunol. 1992 Apr 15;148(8):2572-7.
Pedigree analysis of a Dutch family revealed the presence of an HLA-A "blanc" allele segregating with the HLA-B8, -Cw7, -DR3, -DR52, -DQ2 haplotype. Precipitation studies, using selected mAb and sera directed against conserved epitopes of HLA class I products, failed to detect the expression of a corresponding HLA-A locus product. cDNA nucleotide sequence analysis of the HLA-A "blanc" specificity showed that the obtained sequence was identical to the authentic HLA-A1 gene revealing no mutations, deletions or recombinations that could influence translation or transport of a putative translation product to the cell surface. Mitogen stimulation, EBV transformation, or treatment with rIFN-gamma and rTNF-alpha did not induce HLA-A1 expression. Furthermore, cell-mediated lympholysis analysis revealed that individuals carrying the nonexpressed HLA-A1 gene could mount a strong anti-HLA-A1 T cell response, indicating that HLA-A1 was not expressed during T cell ontogeny. Therefore, this study describes for the first time the allele-specific down-regulation of the expression of a classical HLA class I gene segregating in healthy individuals.
对一个荷兰家族的系谱分析显示,存在一个与HLA - B8、- Cw7、- DR3、- DR52、- DQ2单倍型共分离的HLA - A“空白”等位基因。使用针对HLA I类产物保守表位的选定单克隆抗体和血清进行的沉淀研究未能检测到相应HLA - A基因座产物的表达。对HLA - A“空白”特异性的cDNA核苷酸序列分析表明,获得的序列与真实的HLA - A1基因相同,未发现可能影响假定翻译产物向细胞表面翻译或转运的突变、缺失或重组。丝裂原刺激、EB病毒转化或用重组干扰素 - γ和重组肿瘤坏死因子 - α处理均未诱导HLA - A1表达。此外,细胞介导的淋巴细胞溶解分析表明,携带未表达的HLA - A1基因的个体能够产生强烈的抗HLA - A1 T细胞反应,这表明HLA - A1在T细胞个体发育过程中未表达。因此,本研究首次描述了在健康个体中分离的经典HLA I类基因表达的等位基因特异性下调。