Pera C, Delfino L, Morabito A, Longo A, Johnston-Dow L, White C B, Colonna M, Ferrara G B
National Institute for Cancer Research, IST, Advanced Biotechnology Center, Genova, Italy.
Tissue Antigens. 1997 Oct;50(4):372-9. doi: 10.1111/j.1399-0039.1997.tb02890.x.
In this study we typed HLA-A polymorphisms by a new sequence-based typing (SBT) method, which involved one PCR reaction and four sequencing reactions covering exon 2 and exon 3. This method allowed complete identification of all known HLA-A alleles and revealed the presence of a new allele, named HLA-A*2608. We also introduced sequencing of exon 4 for some samples in order to discriminate the allelic pairs that are identical in exon 2 and 3, thus improving SBT resolution. Finally, we compared the results obtained by SBT with data obtained by serological typing and the amplification refractory mutation system (ARMS-PCR). Together, our results suggest that the SBT here described provides an optimal HLA-A typing technique that may be useful in selecting donor-recipient pairs in bone marrow transplantation between unrelated individuals.
在本研究中,我们采用一种新的基于序列的分型(SBT)方法对HLA - A多态性进行分型,该方法涉及一次聚合酶链反应(PCR)和覆盖外显子2和外显子3的四次测序反应。此方法能够完全鉴定所有已知的HLA - A等位基因,并揭示了一个名为HLA - A*2608的新等位基因的存在。我们还对一些样本进行外显子4测序,以区分在外显子2和3中相同的等位基因对,从而提高SBT分辨率。最后,我们将SBT获得的结果与血清学分型和扩增阻滞突变系统(ARMS - PCR)获得的数据进行比较。总之,我们的结果表明,本文所述的SBT提供了一种最佳的HLA - A分型技术,可能有助于在无关个体间的骨髓移植中选择供受者配对。