Bacteriology Section of the Evandro Chagas Institute, Ministry of Health, Ananindeua, Brasil.
Postgraduate Program in Epidemiology and Health Surveillance of the Evandro Chagas Institute, Ananindeua, Brasil.
J Interferon Cytokine Res. 2021 Mar;41(3):125-131. doi: 10.1089/jir.2018.0162. Epub 2021 Mar 3.
This study aimed at verifying the relationship between the polymorphisms of the cytokines tumor necrosis factor-alpha (TNF-α) -308 G → A (rs1800629); interferon gamma (IFN-γ) +874 T → A (rs2430561); transforming growth factor-beta (TGF-β) códon 10 (rs1982073) and códon 25 (rs1800471); interleukin (IL)-6 - 174 G → C (rs180079) and IL-10 - 1082 A→T (rs1800896); -819 C → T (rs1800871); -592 A→C (rs1800872); and leprosy. Blood samples were analyzed from 106 individuals, of whom 24 were paucibacillary (PB), 28 were multibacillary (MB), and 54 were patient contacts. Analysis of cytokine polymorphisms was typified by the polymerase chain reaction technique. For TGF-β +869 T → C and +915 G→C, a tendency to associate the presence of the C allele at codon 10 with leprosy was demonstrated, with the T allele being most frequently found in the CCOSI ( = 0.056). For the polymorphisms IL-10 - 1082 A→T, -819 C→T, and -592 A→C, we found an association of the GCC/GCC genotype with the susceptibility to the disease and the A allele at position 1082 with the leprosy protection. Greater predominance was found of ACC/ATA (31.3%) and GCC/ATA (37.5%) ( = 0.03) and the A allele at position -1082 (76.85%) ( = 0.043) in the CCOSI groups, whereas the GCC/GCC was found in the MB group (22.2%) ( = 0.05). For the other cytokines's single-nucleotide polymorphisms, there were no associations with susceptibility to leprosy. These results are limited by sample size, may not be conclusive, and will need further confirmation in a larger cohort.
本研究旨在验证细胞因子肿瘤坏死因子-α(TNF-α)-308 G→A(rs1800629);干扰素-γ(IFN-γ)+874 T→A(rs2430561);转化生长因子-β(TGF-β)密码子 10(rs1982073)和密码子 25(rs1800471);白细胞介素(IL)-6-174 G→C(rs180079)和 IL-10-1082 A→T(rs1800896);-819 C→T(rs1800871);-592 A→C(rs1800872);和麻风病之间的关系。从 106 名个体中分析了血液样本,其中 24 名是少菌型(PB),28 名是多菌型(MB),54 名是患者接触者。细胞因子多态性分析采用聚合酶链反应技术。对于 TGF-β+869 T→C 和+915 G→C,我们发现第 10 位密码子 C 等位基因与麻风病存在关联的趋势,T 等位基因最常出现在 CCOSI( = 0.056)中。对于 IL-10-1082 A→T、-819 C→T 和-592 A→C 多态性,我们发现 GCC/GCC 基因型与疾病易感性相关,而 1082 位的 A 等位基因与麻风病保护相关。在 CCOSI 组中,我们发现更多的 ACC/ATA(31.3%)和 GCC/ATA(37.5%)( = 0.03)和位置-1082 的 A 等位基因(76.85%)( = 0.043),而在 MB 组中发现了 GCC/GCC(22.2%)( = 0.05)。对于其他细胞因子的单核苷酸多态性,与麻风病易感性没有关联。这些结果受到样本量的限制,可能不具有结论性,需要在更大的队列中进一步证实。