Obata F, Ito K, Kaneko T, Yang Y G, Onda K, Ito I, Yabe N, Watanabe K, Kashiwagi N
Department of Transplantation Immunology, Kitasato University School of Medicine, Sagamihara, Japan.
Tissue Antigens. 1991 Sep;38(3):124-32. doi: 10.1111/j.1399-0039.1991.tb02025.x.
We determined HLA-DRB types of 375 randomly chosen healthy Japanese donors using a set of 29 different sequence-specific oligonucleotide (SSO) probes directed against various DRB alleles. Except for a few cases, these SSOs enabled us to identify 33 different DRB types including those detectable only by SSO genotyping. Gene frequencies were calculated for each of the DRB types identified. The "blank" frequency calculated by our SSO typing was essentially zero, in contrast to the considerably high "blank" frequencies reported at serological HLA-DR or cellular HLA-D workshops. This indicates that almost all of the DRB types in the Japanese population are positively detectable by our SSO typing. By comparing the gene frequencies for each of the DR types obtained by our SSO typing with those obtained by immunological typing at workshops, significant differences were observed for several of the DR types.
我们使用一组针对各种DRB等位基因的29种不同的序列特异性寡核苷酸(SSO)探针,对375名随机选择的健康日本供者进行了HLA - DRB分型。除少数情况外,这些SSO使我们能够鉴定出33种不同的DRB类型,包括那些仅通过SSO基因分型才能检测到的类型。计算了所鉴定的每种DRB类型的基因频率。通过我们的SSO分型计算出的“空白”频率基本为零,这与血清学HLA - DR或细胞HLA - D分型研讨会上报道的相当高的“空白”频率形成对比。这表明日本人群中几乎所有的DRB类型都能通过我们的SSO分型被阳性检测到。通过将我们的SSO分型获得的每种DR类型的基因频率与研讨会上免疫分型获得的基因频率进行比较,发现几种DR类型存在显著差异。