Crouzet J, Marbach M C, Camus J P, Godeau P, Herreman G, Richier D, Hors J, Dausset J
Nouv Presse Med. 1975 Oct 18;4(35):2489-92.
49 unrelated subjects suffering from systemic scleroderma were typed for 28 HL-A antigens, without any particular significant association of an antigen with the disease or one of its manifestations being noted. In addition, 13 patients from the same family were genotyped for HL-A. Transmission of the disease through 4 generations does not seem to be linked to a particular haplotype and no pair of sibling HL-A identical patients were seen in the same generation. By contrast, two pairs of sibling patients were HL-A different. Nevertheless, other cases, and in particular familial, will be necessary before an association between the genes of susceptibility to S.S. and a gene in the chromosomal HL-A region may be definitely eliminated.
对49名患有系统性硬皮病的非亲属受试者进行了28种HL - A抗原分型,未发现任何一种抗原与该疾病或其任何一种表现有特别显著的关联。此外,对来自同一家庭的13名患者进行了HL - A基因分型。该疾病在4代人中的传递似乎与特定单倍型无关,且在同一代中未发现一对HL - A相同的同胞患者。相比之下,有两对同胞患者的HL - A不同。然而,在明确排除系统性硬皮病易感性基因与染色体HL - A区域基因之间的关联之前,还需要研究其他病例,尤其是家族性病例。