Santana Nadja de Lima, Rêgo Jamile Leão, Oliveira Joyce Moura, Almeida Lucas Frederico de, Braz Marcos, Machado Lídia Maria Medeiros, Machado Paulo Roberto Lima, Castellucci Léa Cristina
Universidade Federal da Bahia, Hospital Universitário Professor Edgard Santos, Serviço de Imunologia, Salvador, BA, Brasil.
Universidade Federal da Bahia, Programa de Pós-Graduação em Ciências da Saúde, Salvador, BA, Brasil.
Mem Inst Oswaldo Cruz. 2017 Apr;112(4):260-268. doi: 10.1590/0074-02760160366. Epub 2017 Mar 2.
Leprosy or hansen's disease is a spectral disease whose clinical forms mostly depends on host's immune and genetic factors. Different Toll-like receptors (TLR) variants have been described associated with leprosy, but with some lack of replication across different populations.
To evaluate the role of polymorphisms in genes TLR1, TLR2 and TLR4 and susceptibility to leprosy in a genetic case control study; to verify the association between genotypes of these markers and the immunological profile in the serum of patients with leprosy.
Pre-designed TaqMan® assays were used to genotype markers at TLR1 (rs4833095, rs5743551), TLR2 (rs7656411, rs3804099) and TLR4 (rs1927914, rs1927911). A panel of cytokines and chemokines was accessed by enzime-linked immunosorbent assay (ELISA) test in the serum of a subgroup of patients with and without leprosy reactions.
Our results show an association between the T allele of rs3804099 at the TLR2 gene and increased risk for leprosy per se [Odds ratio (OR) = 1.296, p = 0,022]. In addition, evaluating the association between different genotypes of the TLR1, 2 and 4 markers and cytokine/chemokine serological levels, IL-17 appears as an immunological marker regulated by the polymorphism of the three TLR genes evaluated, whereas different TLR1 genotypes were associated with differential production of IL-12p40 and MCP-1(CCL2). Furthermore, other relevant serum markers such as CXCL-10 and IL-6 seemed to be regulated by TLR2 variants and IL-1β was related to TLR4 genotypes.
All together our data points that the tested TLR markers may have a regulatory role in the immunity against Mycobacterium leprae, by driving the host's production of key cytokines and chemokines involved in the pathogenesis of this disease.
麻风病或汉森病是一种光谱疾病,其临床形式主要取决于宿主的免疫和遗传因素。已描述了不同的Toll样受体(TLR)变体与麻风病相关,但在不同人群中有些缺乏重复性。
在一项遗传病例对照研究中评估TLR1、TLR2和TLR4基因多态性在麻风病易感性中的作用;验证这些标志物的基因型与麻风病患者血清免疫谱之间的关联。
使用预先设计的TaqMan®分析对TLR1(rs4833095、rs5743551)、TLR2(rs7656411、rs3804099)和TLR4(rs1927914、rs1927911)的标志物进行基因分型。通过酶联免疫吸附测定(ELISA)试验检测一组有或无麻风反应患者亚组血清中的细胞因子和趋化因子。
我们的结果显示,TLR2基因rs3804099的T等位基因与麻风病本身的风险增加相关[比值比(OR)=1.296,p=0.022]。此外,评估TLR1、2和4标志物的不同基因型与细胞因子/趋化因子血清水平之间的关联时,IL-17似乎是受所评估的三个TLR基因多态性调节的免疫标志物,而不同的TLR1基因型与IL-12p40和MCP-1(CCL2)的差异产生相关。此外,其他相关血清标志物如CXCL-10和IL-6似乎受TLR2变体调节,而IL-1β与TLR4基因型相关。
我们的数据总体表明,所测试的TLR标志物可能通过驱动宿主产生参与该疾病发病机制的关键细胞因子和趋化因子,在抗麻风分枝杆菌免疫中发挥调节作用。