African ancestry and innate immunity contribute to the incidence of multicentric Castleman's disease in HIV-1/Kaposi's sarcoma herpesvirus-coinfected individuals

被引:3
|
作者
Westrop, Samantha J. [1 ]
Lagos, Dimitrios [2 ,3 ,4 ]
Boshoff, Chris [2 ]
Bower, Mark [5 ]
Imami, Nesrina [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Med, London, England
[2] UCL, UCL Canc Inst, London, England
[3] Univ York, Dept Biol, York YO10 5DD, N Yorkshire, England
[4] Univ York, Hull York Med Sch, York YO10 5DD, N Yorkshire, England
[5] Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Surg & Canc, London, England
关键词
Kaposi's sarcoma herpesvirus; multicentric Castleman's disease; single nucleotide polymorphism; Toll-like receptor 4; KAPOSIS-SARCOMA; INFECTION; POLYMORPHISMS; RISK; HHV8;
D O I
10.2217/FVL.12.54
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aims: Kaposi's sarcoma herpesvirus (KSHV) is the etiological agent of Kaposi's sarcoma and multicentric Castleman's disease (MCD), a lymphoproliferative disorder associated with high KSHV load. Here, we analyze the frequency of A299G, a TLR4 single nucleotide polymorphism associated with increased MCD incidence, in a cohort of HIV-1(+) individuals, exploring the link between genotype, KSHV disease and ethnicity. Materials & methods: One hundred and seven HIV-1(+) patients presenting with KSHV-related (n = 41) and KSHV-unrelated (n = 66) malignancies were analyzed according to ethnicity, and genotyped for A299G. DNA was extracted from peripheral blood, and the presence of A299G determined by pyrosequencing. Results: Of 41 patients presenting with KSHV-related malignancies, 12 were of African ancestry and 29 of European ancestry. MCD was diagnosed in 18 individuals, 50% of whom had African ancestry. HIV-1(+) individuals with KSHV-related malignancies of African ancestry had a 2.4-fold increased occurrence of MCD compared with European counterparts (relative risk: 2.42; 95% Cl: 1.28-4.55; p = 0.025). A299G was found to be present in 33% of black African and 10% of white European patients with KSHV-related malignancies. In the cohort of patients diagnosed with MCD (n = 18), A299G was present at a frequency of 0.33, regardless of ethnicity. Conclusion: The 2.4-fold higher incidence of MCD in patients of African ancestry presenting with KSHV-related malignancies may be due to the more than three-times higher frequency of A299G compared with that observed in European counterparts. This data highlights a clinically relevant consideration for those caring for KSHV+HIV-1(+) patients of African ancestry, linking genetic variation to disease.
引用
收藏
页码:729 / 734
页数:6
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