FcγRIIa genotype predicts progression of HIV infection

被引:115
作者
Forthal, Donald N.
Landucci, Gary
Bream, Jay
Jacobson, Lisa P.
Phan, Tran B.
Montoya, Benjamin
机构
[1] Univ Calif Irvine, Sch Med, Dept Med, Div Infect Dis, Irvine, CA 92697 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Int Hlth, Dis Prevent & Control Program, Baltimore, MD 21218 USA
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
关键词
D O I
10.4049/jimmunol.179.11.7916
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Polymorphisms in Fc gamma R genes are associated with susceptibility to or severity of a number of autoimmune and infectious diseases. We found that HIV-infected men in the Multicenter AIDS Cohort Study with the Fc gamma RIIa RR genotype progressed to a CD4(+) cell count of <200/mm(3) at a faster rate than individuals with the RH or HH genotypes (relative hazard = 1.6; p = 0.0001). However, progression to AIDS (using the broad definition of either a CD4(+) cell count <200/mm(3) or development of an AIDS-defining illness) was less impacted by Fc gamma RIIa genotype, largely because HH homozygotes had an increased risk of Pneumocystis jiroveci pneumonia as an AIDS-defining illness. We also showed that chronically infected subjects develop a substantial anti-gp120-specific IgG2 response. Moreover, HIV-1 immune complexes are more efficiently internalized by monocytes from HH subjects compared with RR subjects, likely because of the presence of IgG2 in the complexes. Finally, the Fc gamma RIIIa F/V gene polymorphism was not associated with progression of HIV infection, but, as demonstrated previously, did predict the risk of Kaposi's sarcoma. These results demonstrate the importance of Fc gamma Rs in AIDS pathogenesis and point toward a critical role for interactions between Fc gamma Rs and immune complexes in disease progression.
引用
收藏
页码:7916 / 7923
页数:8
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