Although the aetioiogy of chronic fatigue syndrome is controversial, eviden
ce that infective agents including viruses may have a role in the developme
nt of the condition has led to studies seeking an association with the immu
nomodulatory HLA genes. In the present study, we sought to extend previous
work using a well-characterized patient group and modem HLA genotyping tech
niques. Fifty-eight patients were phenotyped for HLA A and B by microcytoto
xicity and genotyped for HLA DRB, DQB and DPB by PCR oligoprobing, and the
frequencies of antigens so assigned were compared with those from a control
group of 134. No significant differences in HLA frequencies were found bet
ween patient and control groups. Thus, this study does not confirm previous
findings of an HLA association with chronic fatigue syndrome, suggesting t
hat neither presentation of viral antigen by HLA class I nor antigen proces
sing genes in the HLA region is a major contributory factor in the developm
ent of the disease.