Polymorphism of HLA‐DRw52‐associated DRB1 genes as defined by sequence‐specific oligonucleotide probe hybridization and sequencing

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Abstract
We have used group‐specific DNA amplification and sequence‐specific oligonucleotide probe (SSOP) hybridization to study DRB1 sequence polymorphisms associated with DR3, DRw11(5), DRwl2(5), DRwl3(w6), DRwl4(w6) and DRw8 alleles. Group‐specific amplification of DRw52‐associated DRB1 alleles was achieved using a 5′ amplification primer designed to hybridize with a first hypervariable region (HVR) sequence common to all known alleles in this group, together with a 3′ intron primer. Prospective SSOP typing of DR3, DRw11, DRwl2, DRwl3, DRwl4 and DRw8 alleles was performed in 318 individuals, including 124 patients, 46 family members and 148 unrelated marrow donors. Among the 395 DRw52‐associated DRB1 alleles tested in our study, a subtype corresponding to the previously defined alleles DRB1*0301–2 (DR3), DRB1*1101–4 (DR5), DRB1*1201–2 (DR5), DRB1*1301–5(DRw6),DRB1*1401–2 and 1404 (DRw6), and DRB1*0801–4 (DRw8) could be assigned in all but 6 individuals (1.9%) tested. In addition to the 22 known alleles, we identified two new DRw6‐associated alleles, DRB1*13.MW(1) and DRB1*14.GB(1). DRB1*13.MW typed serologically as DRwl3 and was identical to DRB1*1301 except at codon 71 where AGG encodes arginine instead of GAG encoding glutamic acid. DRB1*14.GB represents a DRB1*1402 variant whose sequence at codon 86 encodes valine (GTG) instead of glycine (GGT). These results demonstrate that SSOP methods represent an efficient and precise approach for typing DRB1 alleles and for identifying potential novel variants previously unrecognized by conventional typing methods.