Assone Tatiane, de Souza Fernando Vieira, Gaester Karen Oliveira, Fonseca Luiz Augusto Marcondes, Luiz Olinda do Carmo, Malta Fernanda, Pinho João Renato Rebello, Gonçalves Fernanda de Toledo, Duarte Alberto Jose da Silva, de Oliveira Augusto Cesar Penalva, Casseb Jorge
Laboratório de Dermatologia e Imunodeficiências, Departamento de Dermatologia, Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil; Instituto de Medicina Tropical de São Paulo, São Paulo, São Paulo, Brazil.
Instituto de Doenças Infecciosas "Emilio Ribas" (IIER) de São Paulo, São Paulo, São Paulo, Brazil.
PLoS Negl Trop Dis. 2014 Sep 18;8(9):e3199. doi: 10.1371/journal.pntd.0003199. eCollection 2014 Sep.
The polymorphisms of IL28B have been described as important in the pathogenesis of infections caused by some viruses. The aim of this research was to evaluate whether IL28B gene polymorphisms (SNP rs8099917 and SNP rs12979860) are associated with HAM/TSP.
The study included 229 subjects, classified according to their neurological status in two groups: Group I (136 asymptomatic HTLV-1 carriers) and Group II (93 HAM/TSP patients). The proviral loads were quantified, and the rs8099917 and rs12979860 SNPs in the region of IL28B-gene were analyzed by StepOnePlus Real-time PCR System.
A multivariate model analysis, including gender, age, and HTLV-1 DNA proviral load, showed that IL28B polymorphisms were independently associated with HAM/TSP outcome in rs12979860 genotype CT (OR = 2.03; IC95% = 0.96-4.27) and in rs8099917 genotype GG (OR = 7.61; IC95% = 1.82-31.72).
Subjects with SNP rs8099917 genotype GG and rs12979618 genotype CT may present a distinct immune response against HTLV-1 infection. So, it seems reasonable to suggest that a search for IL28B polymorphisms should be performed for all HTLV-1-infected subjects in order to monitor their risk for disease development; however, since this is the first description of such finding in the literature, we should first replicate this study with more HTLV-1-infected persons to strengthen the evidence already provided by our results.
白细胞介素28B(IL28B)的多态性已被描述为在某些病毒引起的感染发病机制中具有重要作用。本研究的目的是评估IL28B基因多态性(单核苷酸多态性rs8099917和单核苷酸多态性rs12979860)是否与热带痉挛性截瘫(HAM/TSP)相关。
该研究纳入了229名受试者,根据其神经状态分为两组:第一组(136名无症状人类嗜T淋巴细胞病毒1型(HTLV-1)携带者)和第二组(93名HAM/TSP患者)。对前病毒载量进行定量,并通过StepOnePlus实时荧光定量PCR系统分析IL28B基因区域中的rs8099917和rs12979860单核苷酸多态性。
一项多变量模型分析,包括性别、年龄和HTLV-1 DNA前病毒载量,显示在rs12979860基因型CT(比值比(OR)=2.03;95%置信区间(IC95%)=0.96 - 4.27)和rs8099917基因型GG(OR = 7.61;IC95% = 1.82 - 31.72)中,IL28B多态性与HAM/TSP结局独立相关。
rs8099917基因型GG和rs12979618基因型CT的受试者可能对HTLV-1感染呈现出不同的免疫反应。因此,建议对所有HTLV-1感染的受试者进行IL28B多态性检测,以监测其疾病发展风险;然而,由于这是文献中对此类发现的首次描述,我们应首先对更多HTLV-1感染的个体重复本研究,以加强我们的结果所提供的证据。