Graduate Program in Health Sciences, Universidade Estadual De Maringá, Maringá, Paraná, Brazil.
Department of Clinical Analysis and Biomedicine- Laboratory of Leishmaniasis, Universidade Estadual De Maringá, Maringá, Paraná, Brazil.
Expert Rev Clin Immunol. 2021 May;17(5):513-537. doi: 10.1080/1744666X.2021.1906650. Epub 2021 Apr 20.
The outcomes of tegumentary leishmaniasis (TL) rely on a complex interaction between the host immune system and the parasite. This study assessed the influence of polymorphisms in immune-related genes on TL.
Web of Science, Scopus, PubMed, and Embase databases were searched systemically. The meta-analysis used a retrospective model in examining alleles, heterozygotes, and homozygotes. A quality assessment and an analysis of cumulative evidence were performed.
A total of 29 genes (encoding for cytokines, chemokines, and other immune receptors) and 84 polymorphisms were analyzed. The IL-1β_rs16944 (OR = 1.341, = 0.003), TNF-α_rs1800629 (OR = 3.804, = 0.004), MIF_rs755622 (OR = 3.357, = 0.001), and INF- γ_rs243056 (OR = 1.670, = 0.028) polymorphisms were speculated as risk factor for TL. They decrease the expression of the corresponding genes crucial for TL control. The quality assessment score was approximately 50%, suggesting the need for a clear method and polymorphism characterization for further comparison. The relevant risk of bias and other considerations resulted in low and moderate cumulative evidence confidence.
IL-1β_rs16944, TNF-α_rs1800629, MIF_rs755622, and INF-γ_rs2430561 polymorphisms were speculated as risk factor for TL, corroborating that IL-1β, TNF-α, INF-γ, and MIF are involved in the TL pathogenesis.
皮肤利什曼病(TL)的结局取决于宿主免疫系统和寄生虫之间的复杂相互作用。本研究评估了免疫相关基因多态性对 TL 的影响。
系统检索了 Web of Science、Scopus、PubMed 和 Embase 数据库。荟萃分析采用回顾性模型来检查等位基因、杂合子和纯合子。进行了质量评估和累积证据分析。
共分析了 29 个基因(编码细胞因子、趋化因子和其他免疫受体)和 84 个多态性。IL-1β_rs16944(OR=1.341, =0.003)、TNF-α_rs1800629(OR=3.804, =0.004)、MIF_rs755622(OR=3.357, =0.001)和 INF-γ_rs243056(OR=1.670, =0.028)多态性被推测为 TL 的危险因素。它们降低了对 TL 控制至关重要的相应基因的表达。质量评估评分约为 50%,表明需要更明确的方法和多态性特征来进一步比较。相关的风险偏倚和其他考虑因素导致了低到中等累积证据可信度。
IL-1β_rs16944、TNF-α_rs1800629、MIF_rs755622 和 INF-γ_rs2430561 多态性被推测为 TL 的危险因素,这表明 IL-1β、TNF-α、INF-γ 和 MIF 参与了 TL 的发病机制。