DNA typing for HLA-DPB1-alleles in German patients with systemic lupus erythematosus using the polymerase chain reaction and DIG-ddUTP-labelled oligonucleotide probes. Members of SLE Study Group

Autor: Z, Yao, K, Hartung, H G, Deicher, G, Brünnler, M P, Bettinotti, E, Keller, C, Paul, C, Gawron, S, Mikschl, E, Albert
Rok vydání: 1993
Předmět:
Zdroj: European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics. 20(4)
ISSN: 0960-7420
Popis: Genomic DNA of 178 German Caucasian patients with systemic lupus erythematosus are studied for HLA-DP locus by using PCR and DIG-ddUTP-labelled oligonucleotide probes. A significant increase of DPB1*0101 is observed in SLE patients compared with healthy controls (chi 2 = 15.27, p.c.0.004). DPB1*0501 and *0901 are also slightly increased (chi 2 = 5.85, P0.05, p.c. = NS; chi 2 = 5.64, P0.05, p.c. = NS). There is no significant difference in frequency of DP alleles between male and female patients. Since a linkage disequilibrium between HLA-B, DR and DP loci is found in our SLE patients, an analysis is performed assessing the relative importance of these HLA-markers to SLE. The results show that the increase of DPB1*0101 in SLE patients is associated with the HLA-B8, DR3 haplotype and it suggests a more important role for HLA-B8, DR3 or genes within this haplotype than for DPB1*0101 in the genetic predisposition for SLE.
Databáze: OpenAIRE