1 Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
2 KingMed School of Laboratory Medicine of Guangzhou Medical University, Guangzhou, China.
Viral Immunol. 2019 Apr;32(3):121-130. doi: 10.1089/vim.2018.0151. Epub 2019 Mar 5.
Dengue virus infection (DEN) is one of the most prevalent arbovirus diseases in the tropical and subtropical areas. Some human leukocyte antigen (HLA) alleles have been reported to be a protective or risk factor to DEN. Due to the limited sample sizes and regional limitations, the results of individual studies were various. This meta-analysis aimed at investigating the relationship between HLA alleles and dengue disease. Relevant studies of the relationship between HLA and dengue disease were searched through PubMed, Embase, Web of science, and Cochrane databases. Subgroups according to ethnicity or sub-alleles and sensitivity analysis were used to explore the potential source of heterogeneity, which was performed to confirm the findings. The relationships between HLA and dengue disease were defined by odds ratios (ORs) with a 95% confidence interval (CI). Fourteen studies were finally confirmed. Results indicated that A0203 (OR = 2.19, 95% CI = 1.30-3.69) and A24 in the Asian group (OR = 1.44, 95% CI = 1.21-1.71) were positively associated with an increased risk of DEN when compared with normal controls. A33 (OR = 0.49, 95% CI = 0.34-0.69) in Southeast Asia was negatively associated with DEN when compared with normal controls, suggesting a protective role against DEN. In addition, DRB111 (OR = 4.10, 95% CI = 1.23-13.69) was positively associated with severe dengue (SD) when compared with dengue fever, whereas DRB103 (OR = 0.48, 95% CI = 0.28-0.82) and DRB109 (OR = 0.73, 95% CI = 0.55-0.96) were negatively associated with SD when compared with normal controls. The meta-analysis confirmed that HLA-A0203, A24, A33, DRB103, DRB109, and DRB111 have significantly affected dengue disease, and the associations are related to race and regions.
登革病毒感染(DEN)是热带和亚热带地区最常见的虫媒病毒病之一。一些人类白细胞抗原(HLA)等位基因已被报道为 DEN 的保护或风险因素。由于样本量有限和区域限制,个别研究的结果各不相同。这项荟萃分析旨在研究 HLA 等位基因与登革热疾病之间的关系。通过 PubMed、Embase、Web of Science 和 Cochrane 数据库检索 HLA 与登革热疾病关系的相关研究。根据种族或亚等位基因进行亚组分析,并进行敏感性分析,以探讨异质性的潜在来源,以确认研究结果。使用比值比(OR)及其 95%置信区间(CI)来定义 HLA 与登革热疾病之间的关系。最终确认了 14 项研究。结果表明,与正常对照组相比,亚洲人群中的 A0203(OR=2.19,95%CI=1.30-3.69)和 A24 与 DEN 风险增加相关。与正常对照组相比,东南亚的 A33(OR=0.49,95%CI=0.34-0.69)与 DEN 呈负相关,提示其对 DEN 具有保护作用。此外,与登革热相比,DRB111(OR=4.10,95%CI=1.23-13.69)与重症登革热(SD)呈正相关,而 DRB103(OR=0.48,95%CI=0.28-0.82)和 DRB109(OR=0.73,95%CI=0.55-0.96)与正常对照组相比与 SD 呈负相关。荟萃分析证实,HLA-A0203、A24、A33、DRB103、DRB109 和 DRB111 对登革热疾病有显著影响,且这些关联与种族和地区有关。