A functional toll-like receptor 8 variant is associated with HIV disease restriction

被引:95
作者
Oh, D. -Y. [1 ]
Taube, S. [1 ,4 ]
Hamouda, O. [4 ]
Kuecherer, C. [4 ]
Poggensee, G. [4 ]
Jessen, H. [5 ]
Eckert, J. K. [1 ]
Neumann, K. [2 ]
Storek, A. [1 ]
Pouliot, M. [6 ,7 ]
Borgeat, P. [6 ]
Oh, N. [1 ,5 ]
Schreier, E.
Pruss, A. [3 ]
Hattermann, K. [7 ]
Schumann, R. R. [1 ]
机构
[1] Charite Univ Med Berlin, Inst Microbiol & Hyg, D-10117 Berlin, Germany
[2] Charite Univ Med Berlin, Dept Med Biometry & Clin Epidemiol, D-10117 Berlin, Germany
[3] Charite Univ Med Berlin, Inst Transfus Med, D-10117 Berlin, Germany
[4] Robert Koch Inst, D-1000 Berlin, Germany
[5] Berlin Trial HIV & TLR SNPs, Berlin, Germany
[6] Ctr Hosp Univ, Quebec Res Ctr, Ctr Rech Rheumatol & Immunol, Quebec City, PQ, Canada
[7] Univ Laval, Fac Med, Quebec City, PQ G1K 7P4, Canada
关键词
D O I
10.1086/590431
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Toll-like receptors (TLRs) play an important role in the innate immune response to pathogens. TLR8 has been found to recognize RNA derived from various viruses, including human immunodeficiency virus (HIV). Presently, very little is known about the influence of TLR8 genetic variation on susceptibility to and progression of HIV disease. Methods and results. We genotyped a population of 782 HIV-positive adults and 550 healthy control subjects for 3 nonsynonymous TLR8 single-nucleotide polymorphisms. We found that the presence of the most frequent TLR8 polymorphism, TLR8 A1G (rs3764880), confers a significantly protective effect regarding progression of the disease. In overexpression assays, we demonstrated that this receptor variant displays impaired NF-kappa B activation in vitro. Furthermore, we analyzed different cell types obtained from individuals differing in their TLR8 genotype and assessed their response to TLR8 ligands in vitro. The presence of the mutated receptor variant was associated with modulation of cytokine secretion profiles and lipid mediator synthesis patterns in monocytes and neutrophils. Conclusions. This first report of a functional TLR8 variant associated with a different clinical course of an RNA viral disease may have implications for the individual risk assessment of patients infected with HIV and other RNA viruses as well as for future HIV vaccine development.
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页码:701 / 709
页数:9
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