Respiratory Medicine
Volume 101, Issue 10 , Pages 2213-2216, October 2007

DQA1*03011 allele: Protective or an adverse effect on the development of sarcoidosis; preliminary study

  • Anna Dubaniewicz

      Affiliations

    • Department of Pathophysiology, Medical University of Gdansk, 80-952 Gdansk, Debinki 7 Street, Poland
    • Corresponding Author InformationCorresponding author. Tel./fax: +48583491510
  • ,
  • Andrzej Dubaniewicz

      Affiliations

    • Ceynowy's Hospital, 84-200 Wejherowo, Jagalskiego 10 Street, Poland
  • ,
  • Ada Dubaniewicz

      Affiliations

    • Department of Clinical Anatomy, Medical University of Gdansk, 80-210 Gdansk, Debinki 1 Street, Poland
  • ,
  • Grażyna Moszkowska

      Affiliations

    • Department of Immunopathology, Medical University of Gdansk, 80-952 Gdansk, Debinki 7 Street, Poland

Received 9 January 2007; accepted 3 June 2007. published online 28 July 2007.

Summary 

Background

Sarcoidosis (SA) is a multisystem granulomatous disorder of unknown etiology. It seems likely that in genetically different predisposed hosts, the same antigen(s) may cause the development of sarcoid Th1 response. The interaction of the T-cell receptor with the human leukocyte antigen-DQA1*03011 peptide-complex can affect T lymphocytes activation in a dose-response manner.

Objectives/Methods

To test occurrence of DQA1*03011 allele in SA, we compared the distribution of DQA1 alleles in 32 SA patients, 37 TB patients and in 58 healthy volunteers, using a PCR-SSP “high-resolution” method.

Results

Our results revealed that after Bonferroni correction DQA1*03011 were less common in SA patients than in the controls (OR 0.16, 95%CI 0.03–0.75). In TB, DQA1*0303 were significantly more frequent and DQA1*0505 less present as compared to the controls (OR 11.03, 95% CI 1.20–95.80, OR 0.29, 95% CI 0.01–0.88). Comparing DQA1 alleles in both patient groups, DQA1*0501, DQA1*0505 alleles were more common and DQA1*03011, DQA1*0302, DQA1*0303 were less common after Bonferroni correction in SA than in TB.

Conclusion

We revealed that DQA1*03011 allele was less common in SA than in the controls and TB. It seems possible that a low frequency of DQA1*03011 occurrence may be also involved in the etiopathogenesis of SA.

Keywords: DQA1*03011, Sarcoidosis, Tuberculosis

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PII: S0954-6111(07)00256-9

doi:10.1016/j.rmed.2007.06.004

Respiratory Medicine
Volume 101, Issue 10 , Pages 2213-2216, October 2007