Volume 53, Issue 12 pp. 1460-1463
Report

Allelic variation in HLA-DRB1* loci in Syrian pemphigus vulgaris patients

Elham Harfouch MD, PhD

Corresponding Author

Elham Harfouch MD, PhD

Laboratory for Research and Genetic Consultation, Faculty of Medicine, University of Damascus, Damascus, Syria

Correspondence

Elham Harfouch, md, phd

Laboratory for Research and Genetic Consultation

Faculty of Medicine, University of Damascus

Mazzeh Autostrad, Damascus, Syria

E-mail: [email protected]

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Saleh Daoud MD

Saleh Daoud MD

Department of Dermatology, University of Damascus Hospital, Damascus, Syria

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First published: 02 April 2014
Citations: 8
Funding: University of Damascus.
Conflicts of interest: None.

Abstract

Background

Pemphigus vulgaris (PV) is known to be strongly associated with particular alleles of the human leukocyte antigen (HLA)-DRB1* loci. However, to date, the association of HLA with pemphigus has not been studied in a Syrian population.

Objectives

We aimed to study HLA-DRB1* loci variation in Syrian PV patients.

Methods

We used a sequence-specific primer polymerase chain reaction method to define the allele type of the DRB1* loci in 91 patients with PV and 270 healthy control subjects.

Results

We noticed an increased frequency of HLA-DRB1*04 and DRB1*14 alleles in patients with PV compared with healthy control subjects (67.0% vs. 26.3%; odds ratio [OR] = 5.7, corrected < 0.0001 for DRB1*04; 54.9% vs. 11.0%; OR = 9.5, corrected < 0.0001 for DRB1*14). Among DRB1*04-positive PV patients, the DRB1*402 subtype was markedly increased compared with DRB1*04-positive healthy controls (84.3% vs. 26.7%; corrected = 0.002), whereas the DRB1*0403 variant was represented more commonly in DRB1*04-positive healthy individuals than in DRB1*04-positive PV patients (45.0% vs. 1.6%; corrected < 0.0001). In addition, the frequency of DRB1*11 was significantly decreased in PV patients compared with healthy controls (19.7% vs. 50.4%; OR = 0.25, corrected < 0.0001).

Conclusions

The occurrence of PV is positively associated with HLA-DRB1*14 and HLA-DRB1*0402 but negatively associated with HLA-DRB1*11 in the Syrian population.

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