Ocular cicatricial pemphigoid (OCP) is an autoimmune blistering disease that affects the conjunctiva and multiple mucous membranes. Class I and H and complement genetic markers of the major histocompatibility complex were studied in 20 Caucasian OCP patients and members of their families. Frequencies of individual alleles and common fixed or extended haplotypes in the patients were compared with those in normal family control haplotypes and with overall normal Caucasian haplotypes. The most striking increase compared with overall controls was noted in HLA-DQw3 (P = 0.006), unassociated with any extended haplotype. All but 1 of the 20 patients carried DQw3 in linkage with HLA-DR4 (increased significantly with P = 0.042 compared with overall normal genotype controls) or DR5. The DQw3, on analysis by restriction fragment length polymorphism in genomic DNA, was, in every instance, DQw7 (3.1, DQB1*0301). The frequency of DQB1*0301 in patient haplotypes compared with overall normal DR4 and DR5 DQw3-bearing haplotypes was statistically significantly increased (P < 0.003, relative risk = 9.6). The distribution of homozygotes and heterozygotes for DQB1*0301 among the patients was consistent with dominant but not recessive inheritance of DQB1*0301 or a gene, probably a class H allele, in linkage disequilibrium with it as the major histocompatibility complex susceptibility gene for OCP.Ocular cicatricial pemphigoid (OCP) is an autoimmune blistering disease that affects multiple mucous membranes (1-3). If not treated or treated inappropriately when it affects the eyes, it can cause blindness. The pathologic processes of chronic cicatrizing conjunctivitis and progressive conjunctival subepithelial fibrosis that characterize this disease result in severe xerosis of the eye and ocular keratinization.The deposition of immunoglobulins and complement components at the basement membrane zone (BMZ) (4-6) of the involved mucosa appears to be pathogenetic. Inflammatory mediators in the preocular tear film contribute to the final pathologic changes (3). Circulating antibodies to BMZ have been demonstrated in the serum of OCP patients, using skin and buccal mucosa as substrate (7,8).There have only been a few studies of HLA antigen frequencies in patients with OCP. The initial reports (6, 9) of an increased frequency of HLA-B12 (HLA-B44 or B45) were not confirmed in later studies (3, 10). Recently (11), we reported an increase in the frequency of the HLA-DR4 allele in OCP patients. In patients with pemphigus vulgaris, the increased frequency of DR4 is ascribable to the increased frequency oftwo haplotypes, SC21, DR4, DQw8] and SC31, DR4, DQw8], particularly in Ashkenazi Jewish patients (12). The first of these is a known extended haplotype (13) (a haplotype with fixed DNA over at least the HLA-B/DR interval) in this ethnic group. In a number of major histocompatibility complex (MHC) alleleassociated diseases, the increase in specific alleles is secondary to the increase in one or more extended haplotypes that carry suscepti...
We reviewed the charts of 10 patients who were admitted to the Massachusetts Eye and Ear Infirmary over a 10-year period with the diagnosis of Bacillus species endophthalmitis.
HLA typing for A, B, and C locus antigens was performed on 70 patients with ocular cicatricial pemphigoid (OCP) and on 1849 controls. Additionally, typing for DR and DQ antigens and for the complement proteins (C2, factor B, C4A, and C4B) was performed on 63 patients and on the same control population. A significantly higher incidence of the following antigens was found in the OCP patients when compared to the control population: DR4 (43% in patients compared to 18% in controls, p = 0.0001); DR5 (41% compared to 16%, p = 0.0001); DQw3 (57% compared to 31%, p = 0.0010); A2 (60% compared to 28%, p = 0.0001); B8 (24% compared to 13%, p = 0.0086); B35 (19% compared to 9%, p = 0.0097); and B49 (7% compared to 2%, p = 0.0052). The complement types SC01, SC30, SC32, SC41, and SC42 were also significantly increased in patients compared to controls. No significant differences were found based on ethnic background, involvement of multiple mucous membranes, history of glaucoma, or deposition of specific immunoreactants in conjunctival biopsy samples. These findings may provide further insights into the pathogenesis of OCP and may help to localize a susceptibility gene for this autoimmune disease.
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