
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:creator id="https://orcid.org/0000-0002-4652-7719">Dobrijević, Zorana</dc:creator>
  <dc:creator id="https://orcid.org/0000-0003-2042-0056">Nedić, Olgica</dc:creator>
  <dc:creator id="https://orcid.org/0000-0003-2570-1295">Tomić, Sergej</dc:creator>
  <dc:creator id="https://orcid.org/0000-0001-6417-8711">Miljuš, Goran</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-2539-4507">Penezić, Ana</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-0940-9481">Šunderić, Miloš</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-8691-2486">Gligorijević, Nikola</dc:creator>
  <dc:language>eng</dc:language>
  <dc:description xml:lang="eng">ABSTRACT
Due to their pivotal role in orchestrating the immune response, HLA loci were recognized as candidates for genetic association studies related to the severity of COVID-19. Since the findings on the effects of HLA alleles on the outcome of SARS-CoV-2 infection remain inconclusive, we aimed to elucidate the potential involvement of genetic variability within HLA loci in the molecular genetics of COVID-19 by classifying the articles according to different disease severity/outcomes and by conducting a systematic review with meta-analysis. Potentially eligible studies were identified by searching PubMed, Scopus and Web of Science literature databases. A total of 28 studies with 13,073 participants were included in qualitative synthesis, while the results of 19 studies with 10,551 SARS-CoV-2 positive participants were pooled in the meta-analysis. According to the results of quantitative data synthesis, association with COVID-19 severity or with the lethal outcome was determined for the following alleles and allele families: HLA-A*01, HLA-A*03, HLA-A*11, HLA-A*23, HLA-A*31, HLA-A*68, HLA-A*68:02, HLA-B*07:02, HLA-B*14, HLA-B*15, HLA-B*40:02, HLA-B*51:01, HLA-B*53, HLA-B*54, HLA- B*54:01, HLA-C*04, HLA-C*04:01, HLA-C*06, HLA-C*07:02, HLA-DRB1*11, HLA-DRB1*15, HLA-DQB1*03 and HLA-DQB1*06 (assuming either allelic or dominant genetic model). We conclude that alleles of HLA-A, -B, -C, -DRB1 and -DQB1 loci may represent potential biomarkers of COVID-19 severity and/or mortality, which needs to be confirmed in a larger set of studies.</dc:description>
  <dc:description xml:lang="srp">Sažetak</dc:description>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:26193</dc:identifier>
  <dc:identifier>doi:10.1002/rmv.2378</dc:identifier>
  <dc:format>application/pdf</dc:format>
  <dc:format>10956 bytes</dc:format>
  <dc:publisher>John Wiley &amp; Sons Ltd</dc:publisher>
  <dc:title xml:lang="eng">The association of human leucocyte antigen (HLA) alleles with COVID-19 severity: A systematic review and meta-analysis</dc:title>
  <dc:rights>All rights reserved</dc:rights>
  <dc:subject xml:lang="eng">COVID-19, HLA-A, HLA-B, HLA-C, HLA-DQB1, HLA-DRB1</dc:subject>
  <dc:source>Reviews in Medical Virology</dc:source>
  <dc:date>2022</dc:date>
</oai_dc:dc>
