BACKGROUND Multiple studies have implicated a role for CD8+T cell-mediated immune response to
autoantigens in
vitiligo. However, the
antigen-specific T lymphocyte reactivity against the
peptide epitopes is diverse among different world populations. This study aimed to identify the risk
HLA-A allele in
vitiligo and study CD8+ T cell reactivity to 5 autoantigenic
peptides in Han Chinese populations, and to analyze the association of CD8+ T cell reactivity with disease characteristics. MATERIAL AND METHODS The risk
HLA-A allele was analyzed by case-control study.
Enzyme linked immunospot (ELISPOT) assay was used to compare T cell reactivity to the 5 autoantigenic
peptides between
vitiligo patients and healthy controls, then we analyzed the association of CD8+ T cell reactivity to 2 positive
peptides with disease activity and area of skin lesions. RESULTS The results indicated that the most frequent allele in the Han Chinese
vitiligo patients was the
HLA-A*02: 01 allele with a significantly higher frequency compared to controls (20.20% versus 13.79%, P=6.64×10-5). The most frequently encountered
epitopes were 2 gp100 modified
peptides, IMDQVPFSV and YLEPGPVTV, whereas a weak T cell reactivity against
tyrosinase and
Melan-A/MART-1 were evaluated. Moreover, we demonstrated that T cell reactivity against the 2 positive
peptides was significantly associated with disease characteristics including disease activity and area of skin lesions. CONCLUSIONS Our findings showed that the
HLA-A*02: 01 allele was the major risk
HLA-A allele, and 2 gp100 modified
peptides were identified as
autoantigens and were found to be closely related to disease characteristics which might play a critical role in Han Chinese
vitiligo patients.