Role of HLA alleles polymorphism in systemic lupus erythematosus: A prospective study from North India.

Indian J Pathol Microbiol

Department of Pathology, Institute of Medical Sciences (IMS), Banaras Hindu University (BHU), Varanasi, Uttar Pradesh, India.

Published: November 2023

AI Article Synopsis

  • Systemic lupus erythematosus (SLE) is a chronic autoimmune disease influenced by genetic factors and environmental triggers, particularly the role of HLA class II alleles.
  • In a study involving 100 SLE patients and 100 healthy controls, specific HLA alleles were analyzed through PCR to assess their association with SLE susceptibility and protection.
  • The study found that alleles like DRβ1*0301, DRβ1*0701, and DQβ1*0202 were linked to increased risk for SLE, while others like DRβ1*0401 and DQβ1*0501 appeared to offer protective effects against the disease.

Article Abstract

Background: Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder and has complex etiopathogenesis. The most appropriate hypothesis states that genetic susceptibility in the presence of environmental risk factors predisposes to SLE. HLA class II alleles are critical to immune response and are highly polymorphic. Various alleles in HLA-DR and -DQ regions were analyzed in SLE patients and healthy controls to see their role in susceptibility or protection to SLE.

Materials And Methods: This was a prospective observational study, in which a total of 100 SLE patients and 100 controls were analyzed. HLA typing was done by polymerase chain reaction (PCR)-sequence-specific oligonucleotide (SSO) method (SSO probe).

Results: DRβ1*0301 was significantly increased in SLE patients when compared to controls and had the highest odds ratio. Other risk factor alleles found to be increased were DRβ1*0701, DQβ1*0202, and DQβ1*0301, which had a significant positive association with SLE, suggesting their role in susceptibility to SLE. In contrast, DRβ1*0401, DRβ1*1401, DRβ1*1404, DRβ1*1501, DQβ1*0501, and DQα1*0201 showed statistically significant reduction in SLE patients, while these were much more common in controls, suggesting their protective role.

Conclusion: This study is only the second study in patients from North India and it determines the role of DRβ1*0301, DRβ1*0701, DQβ1*0202, and DQβ1*0301 alleles as risk factors in SLE patients.

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Source
http://dx.doi.org/10.4103/ijpm.ijpm_764_21DOI Listing

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