HLA genes as modifiers of response to IFN-β-1a therapy in relapsing-remitting multiple sclerosis

Pharmacogenomics. 2016 Apr;17(5):489-98. doi: 10.2217/pgs.16.2. Epub 2016 Mar 29.

Abstract

Aims: This study investigated the influence of HLA class-I and -II genes in the response to IFN-β in relapsing-remitting multiple sclerosis (MS) patients.

Patients & methods: In this cohort, 231 relapsing-remitting MS patients who are classified into IFN-β responders (n = 146) and nonresponders (n = 85) and 180 ethnic-matched healthy controls were analyzed. Clinical outcome of IFN-β therapy particularly Expanded Disability Status Scale scores were evaluated in relation to HLA-A, -B and -DRB1 alleles and haplotypes.

Results: Increased frequencies of HLA-DRB1*04 allele and HLA-A*03-B*44-DRB1*04 haplotype, and decreased frequency of HLA-B*15 were associated with better response to IFN-β treatment.

Conclusion: The possibility of genetic screening particularly HLA typing prior to starting IFN-β therapy for MS may permit the identification of likely responders or nonresponders.

Keywords: HLA; IFN-β; multiple sclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Female
  • HLA-A Antigens / genetics*
  • HLA-B Antigens / genetics*
  • HLA-DRB1 Chains / genetics*
  • Haplotypes
  • Humans
  • Interferon beta-1a / therapeutic use*
  • Male
  • Multiple Sclerosis, Relapsing-Remitting / drug therapy*
  • Multiple Sclerosis, Relapsing-Remitting / genetics
  • Prospective Studies

Substances

  • HLA-A Antigens
  • HLA-B Antigens
  • HLA-DRB1 Chains
  • Interferon beta-1a