HIV/AIDS & Global Health Research Programme, University of Venda, Thohoyandou 0950, South Africa.
Department of Medical Laboratory Sciences, Kenyatta University, Nairobi 34556-00100, Kenya.
Viruses. 2018 Aug 27;10(9):458. doi: 10.3390/v10090458.
Human herpes virus type 8 (HHV-8) is the causative agent of Kaposi's sarcoma (KS). We systematically reviewed literature published between 1998 and 2017, according to the PRISMA guidelines, to understand the distribution of HHV-8 infection in Africa. More than two-thirds (64%) of studies reported on seroprevalence and 29.3% on genotypes; 9.5% were on both seroprevalence and genotypes. About 45% of African countries had data on HHV-8 seroprevalence exclusively, and more than half (53%) had data on either seroprevalence or genotypes. Almost half (47%) of the countries had no data on HHV-8 infection. There was high heterogeneity in the types of tests and interpretation algorithms used in determining HHV-8 seropositivity across the different studies. Generally, seroprevalence ranged from 2.0% in a group of young children in Eritrea to 100% in a small group of individuals with KS in Central African Republic, and in a larger group of individuals with KS in Morocco. Approximately 16% of studies reported on children. Difference in seroprevalence across the African regions was not significant (95% CI, χ² = 0.86; = 0.35), although specifically a relatively significant level of infection was observed in HIV-infected children. About 38% of the countries had data on K1 genotypes. K1 genotypes A, A5, B, C, F and Z occurred at frequencies of 5.3%, 26.3%, 42.1%, 18.4%, 5.3% and 2.6%, respectively. Twenty-three percent of the countries had data for K15 genotypes, and genotypes P, M and N occurred at frequencies of 52.2%, 39.1%, and 8.7%, respectively. Data on HHV-8 inter-genotype recombinants in Africa are scanty. HHV-8 may be endemic in the entire Africa continent but there is need for a harmonized testing protocol for a better understanding of HHV-8 seropositivity. K1 genotypes A5 and B, and K15 genotypes P and M, from Africa, should be considered in vaccine design efforts.
人疱疹病毒 8 型(HHV-8)是卡波济肉瘤(KS)的致病因子。我们根据 PRISMA 指南系统地回顾了 1998 年至 2017 年间发表的文献,以了解非洲 HHV-8 感染的分布情况。超过三分之二(64%)的研究报告了血清流行率,29.3%报告了基因型;9.5%的研究同时报告了血清流行率和基因型。约 45%的非洲国家仅拥有关于 HHV-8 血清流行率的数据,超过一半(53%)的国家拥有血清流行率或基因型的数据。近一半(47%)的国家没有 HHV-8 感染的数据。在不同的研究中,用于确定 HHV-8 血清阳性的检测类型和解释算法存在高度异质性。总的来说,血清流行率范围从厄立特里亚一组幼儿中的 2.0%到中非共和国一小群卡波济肉瘤患者中的 100%,以及摩洛哥一大群卡波济肉瘤患者中的 100%。大约 16%的研究报告了儿童的数据。非洲各地区血清流行率之间没有显著差异(95%CI,χ²=0.86;P=0.35),尽管在感染 HIV 的儿童中观察到了相对较高的感染水平。约 38%的国家有 K1 基因型的数据。K1 基因型 A、A5、B、C、F 和 Z 的频率分别为 5.3%、26.3%、42.1%、18.4%、5.3%和 2.6%。23%的国家有 K15 基因型的数据,基因型 P、M 和 N 的频率分别为 52.2%、39.1%和 8.7%。非洲关于 HHV-8 基因型间重组的数据很少。HHV-8 可能在整个非洲大陆流行,但需要制定协调一致的检测方案,以更好地了解 HHV-8 血清阳性率。来自非洲的 K1 基因型 A5 和 B,以及 K15 基因型 P 和 M,应在疫苗设计工作中加以考虑。