Department of Bioscience and Bioinformatics, Khallikote University, Berhampur, India.
Department of Biochemistry, SVP Post-Graduate Institute of Pediatrics, Cuttack, Odisha, India.
Lupus. 2021 Feb;30(2):219-227. doi: 10.1177/0961203320972799. Epub 2020 Nov 11.
Cluster of differentiation 14 (CD14) plays a crucial role in the innate immune response of the host in protection against various pathogens. The importance of soluble CD14 in autoimmune disorders has been described in different populations. However, the role of sCD14 in systemic lupus erythematosus (SLE) is poorly understood. Further, the association of functional variants at the promoter region of the CD14 gene (-159 C > T) with susceptibility to SLE or disease severity needs to be defined.
Two hundred female SLE patients diagnosed on systemic lupus international collaborating clinics (SLICC) classification criteria and age, sex, matched healthy controls were enrolled in the present study. Polymerase chain reaction- restriction fragment length polymorphism (PCR-RFLP) method was used to genotype CD14 (C-159 T) polymorphism. Plasma levels of IFN-α, TNF-α, and sCD14 were quantified by enzyme-linked immunosorbent assay (ELISA).
Prevalence of mutant genotypes (CT and TT) and minor allele (T) of CD14 (C-159T) polymorphism was significantly higher in SLE cases compared to healthy controls (CT: P < 0.0001; OR = 3.26, TT:P < 0.0001; OR = 3.39; T:P = 0.0009, OR = 1.62). Further, lupus nephritis patients had a higher prevalence of homozygous mutants (TT) and mutant allele (T)(TT: P = 0.0002, OR = 8.07; T: P = 0.001, OR = 1.32). SLE patients displayed significantly increased plasma sCD14, TNF-α, and IFN-α levels in comparison to healthy controls. These cytokines were significantly elevated in patients of lupus nephritis compared to those without kidney involvement. Interestingly, sCD14 levels correlated positively with SLE disease activity index-2K (SLEDAI-2K) scores and 24 hours proteinuria.
CD14 (C-159T) polymorphism is associated with an increased predisposition to the development of SLE and lupus nephritis: sCD14 is a promising novel biomarker for assessing disease activity and lupus nephritis.
分化群 14(CD14)在宿主对各种病原体的固有免疫反应中起着至关重要的作用。可溶性 CD14 在自身免疫性疾病中的重要性在不同人群中已有描述。然而,CD14 在系统性红斑狼疮(SLE)中的作用仍知之甚少。此外,需要确定 CD14 基因启动子区域的功能变体(-159C>T)与 SLE 的易感性或疾病严重程度之间的关联。
本研究纳入了 200 名女性 SLE 患者和年龄、性别匹配的健康对照者,这些患者均根据系统性红斑狼疮国际合作诊所(SLICC)分类标准进行诊断。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测 CD14(C-159T)多态性的基因型。通过酶联免疫吸附试验(ELISA)定量测定 IFN-α、TNF-α 和 sCD14 的血浆水平。
与健康对照组相比,SLE 患者中突变基因型(CT 和 TT)和 CD14(C-159T)多态性的次要等位基因(T)的发生率显著更高(CT:P<0.0001;OR=3.26;TT:P<0.0001;OR=3.39;T:P=0.0009;OR=1.62)。此外,狼疮肾炎患者的纯合突变体(TT)和突变等位基因(T)的发生率更高(TT:P=0.0002;OR=8.07;T:P=0.001;OR=1.32)。与健康对照组相比,SLE 患者的血浆 sCD14、TNF-α 和 IFN-α 水平显著升高。与无肾脏受累的患者相比,狼疮肾炎患者的这些细胞因子水平显著升高。有趣的是,sCD14 水平与 SLE 疾病活动指数-2K(SLEDAI-2K)评分和 24 小时蛋白尿呈正相关。
CD14(C-159T)多态性与 SLE 和狼疮肾炎的易感性增加有关:sCD14 是评估疾病活动和狼疮肾炎的有前途的新型生物标志物。