Hasanoor Reja Abu Hena, De Abhishek, Chakraborty Disha, Ahmed Sk S, Sarda Aarti
From the Department of Biochemistry, IPGMER, Kolkata, West Bengal, India.
Department of Dermatology, Calcutta National Medical College, Kolkata, West Bengal, India.
Indian J Dermatol. 2023 Nov-Dec;68(6):724. doi: 10.4103/ijd.ijd_386_23. Epub 2024 Jan 9.
Leprae bacilli are identified as foreign by pattern recognition receptors (PRRs) present in the microbes but absent in the host. The Nucleotide oligomerization domain (NOD)-like receptor (NLR) family comprises the nucleotide-binding oligomerisation domain (NOD1 and NOD2) proteins, which are two well-known PRRs. The objectives of this study were to study the expression of cytoplasmic NOD1 and NOD2 in the pathogenesis of leprosy and the serum level of expressed cytokines and to measure the messenger Ribonucleic Acid (mRNA) expression.
Clinically suspected Hansen's patients were analysed for 4 years. Newly diagnosed leprosy patients were considered leprosy disease control (LDC). The cases with active or new lesions and an increase in Bacteriological index (BI) by at least 2 + after 12 months of completion of Multidrug therapy (MDT) were considered leprosy disease relapse (LDR) cases. Age- and sex-matched healthy individuals served as our control group (healthy control (HC)). enzyme-linked immunosorbent assay (ELISA) was performed to measure the concentration of five human cytokines in serum, including three pro-inflammatory cytokines (Tumor necrosis factor (TNF)-α, Interferon gamma (IFN-γ) and IL-6), one anti-inflammatory cytokine (IL-10) and one chemokine (IL-8). Quantitative expression of receptor genes (NOD1 and NOD2) and cytokine genes (TNF-α, IFN-γ, IL-6, IL-10 and IL-8) was evaluated by quantitative real-time polymerase chain reaction (PCR) (qRT-PCR). We studied NOD1 and NOD2 expression in the tissues through fluorescence immunohistochemistry. Differential NLR intracellular expression on peripheral blood monocytes (PBMs) and their response to stimulation with specific ligands (lipopolysaccharide (LPS) and muramyl dipeptide (MDP)) were studied.
A significant difference in the expression of the NOD1 gene was observed in unstimulated monocytes of the LDC and LDR cases when compared to HC. The NOD2 transcript level was significantly higher in stimulated monocytes from LDC and LDR patients than in similarly stimulated cells from HC. The LDC patients had a significantly higher level of pro-inflammatory cytokines as compared to the HC.
In conclusion, this study has demonstrated the expression of both cytokines and chemokines in response to NLR activation in the skin of leprosy patients.
麻风杆菌被微生物中存在但宿主中不存在的模式识别受体(PRR)识别为外来物。核苷酸寡聚化结构域(NOD)样受体(NLR)家族包括核苷酸结合寡聚化结构域(NOD1和NOD2)蛋白,它们是两种著名的PRR。本研究的目的是研究细胞质NOD1和NOD2在麻风病发病机制中的表达以及表达的细胞因子的血清水平,并测量信使核糖核酸(mRNA)的表达。
对临床疑似汉森病患者进行了4年的分析。新诊断的麻风病患者被视为麻风病疾病对照(LDC)。在完成多药治疗(MDT)12个月后,有活动性或新病变且细菌学指数(BI)至少增加2+的病例被视为麻风病疾病复发(LDR)病例。年龄和性别匹配的健康个体作为我们的对照组(健康对照(HC))。进行酶联免疫吸附测定(ELISA)以测量血清中五种人类细胞因子的浓度,包括三种促炎细胞因子(肿瘤坏死因子(TNF)-α、干扰素γ(IFN-γ)和白细胞介素-6)、一种抗炎细胞因子(白细胞介素-10)和一种趋化因子(白细胞介素-8)。通过定量实时聚合酶链反应(PCR)(qRT-PCR)评估受体基因(NOD1和NOD2)和细胞因子基因(TNF-α、IFN-γ、白细胞介素-6、白细胞介素-10和白细胞介素-8)的定量表达。我们通过荧光免疫组织化学研究了组织中NOD1和NOD2的表达。研究了外周血单核细胞(PBM)上NLR细胞内表达的差异及其对特定配体(脂多糖(LPS)和胞壁酰二肽(MDP))刺激的反应。
与HC相比,在LDC和LDR病例未刺激的单核细胞中观察到NOD1基因表达存在显著差异。LDC和LDR患者刺激后的单核细胞中NOD2转录水平明显高于HC中类似刺激的细胞。与HC相比,LDC患者的促炎细胞因子水平明显更高。
总之,本研究证明了麻风病患者皮肤中细胞因子和趋化因子在NLR激活后的表达。