van Dijk A, Melchers R, Hilkes Y, Rozemuller E, Tilanus M
Department of Pathology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Tissue Antigens. 2007 Apr;69 Suppl 1:61-3. doi: 10.1111/j.1399-0039.2006.760_4.x.
Several human leukocyte antigen (HLA)-DRB protocols for sequencing-based typing have been described. In general, the DRB1 amplification is performed using group-specific amplification primers (GSAPs) located in HVR I or intron 1. Only some protocols include amplification of DRB3, DRB4, and DRB5. However, prior knowledge obtained by alternative methods such as PCR-SSP is preferred for some protocols and a large amount of DNA is often required for adequate typing of HLA-DRB1. We describe a new protocol that uses GSAPs located in the introns, includes also sequencing of exon 3 to enable high resolution. This protocol allows DRB typing without prior knowledge of the HLA type.
已经描述了几种基于测序分型的人类白细胞抗原(HLA)-DRB方案。一般来说,DRB1扩增是使用位于高变区I或内含子1中的组特异性扩增引物(GSAP)进行的。只有一些方案包括DRB3、DRB4和DRB5的扩增。然而,对于一些方案,通过诸如PCR-SSP等替代方法获得的先验知识是优选的,并且对于HLA-DRB1的充分分型通常需要大量的DNA。我们描述了一种新方案,该方案使用位于内含子中的GSAP,还包括外显子3的测序以实现高分辨率。该方案允许在无需事先了解HLA类型的情况下进行DRB分型。