Chan L S, Wang T, Wang X S, Hammerberg C, Cooper K D
Department of Dermatology, University of Michigan School of Medicine, Ann Arbor.
Dermatology. 1994;189 Suppl 1:99-101. doi: 10.1159/000246943.
Two factors, is classification and its immunogenetics, may have contributed to an incomplete understanding of the pathogenic mechanism in the disease group commonly termed 'cicatricial pemphigoid'. We have previously demonstrated that pure ocular cicatricial pemphigoid (OCP) is a unique clinical and immunopathological entity. In an effort to better define the immunogenetic characteristics for patients with pure OCP, we performed HLA typing for the class II MHC gene HLA-DQB10301 allele, by amplifying genomic DNA extracted from patients with polymerase chain reaction, followed by hybridization with a sequence-specific oligonucleotide probe on dot-blotted and Southern-blotted amplified DNA samples. Ninety percent (9/10) of patients with pure OCP had the DQB10301 allele, in contrast to 52% (17/33) of normal individuals who had the DQB10301 allele. The high frequency of the HLA-DQB10301 allele in patients with pure OCP may point to a distinct immunogenetic pattern and possibly a distinct pathomechanism for the disease.
