Fachin Luciana Raquel Vincenzi, Soares Cleverson Teixeira, Belone Andrea de Faria Fernandes, Trombone Ana Paula Favaro, Rosa Patrícia Sammarco, Guidella Cássio Cesar, Franco Marcello Fabiano
Laboratory of Anatomic Pathology, Instituto Lauro de Souza Lima, Bauru, São Paulo, Brazil.
Department of Health Science, Universidade do Sagrado Coração, Bauru, São Paulo, Brazil.
Histol Histopathol. 2017 Apr;32(4):385-396. doi: 10.14670/HH-11-804. Epub 2016 Jul 22.
In situ immunophenotyping of leprosy lesions can improve our understanding of the biology of inflammatory cells during the immune response to Mycobacterium leprae antigens. In the present study, biopsies from 10 healthy controls and 70 leprosy patients were selected, 10 for each of the following conditions: clinical tuberculoid (TT), borderline tuberculoid (BT), borderline borderline (BB), borderline lepromatous (BL), lepromatous (LL), reversal reaction (R1), and erythema nodosum leprosum (R2). Qualitative and quantitative immunohistochemical analyses were performed to detect CD3, CD4, CD8, FoxP3, CD20, CD138, CD1a, CD57, CD15, CD117, CD68, and CD163. In addition, histochemistry was employed to identify eosinophils. The amount of CD3+ and CD4+ T cells was higher in TT than in LL patients. CD8+ T cells were predominant in T lymphocyte infiltrations in the basal layer of the epidermis. The number of FoxP3+ cells was similar among different forms of the disease, but was higher in BL and LL than in R2 individuals. CD20+ lymphocytes were most abundant in TT samples, while CD138+ plasma cells displayed no detectable differences. Epithelioid macrophages from the center of TT and R1 granulomas exhibited the M1 phenotype (CD68+CD163-), whereas those in LL granulomas showed the M2 phenotype (CD68+CD163+). There was a gradual decrease in the amount of CD1a+ cells from the TT towards the LL form of the disease. A significant increase in the number of neutrophils was observed only in R2 samples. All the cells investigated, except eosinophils, participated in the immunopathogenesis of leprosy.
麻风病损的原位免疫表型分析可增进我们对麻风分枝杆菌抗原免疫应答过程中炎症细胞生物学特性的理解。在本研究中,选取了10名健康对照者和70名麻风病患者的活检样本,每种情况各10例:临床结核样型(TT)、界线结核样型(BT)、中间界线型(BB)、界线类偏瘤型(BL)、瘤型(LL)、反应期(R1)和麻风结节性红斑(R2)。进行了定性和定量免疫组织化学分析以检测CD3、CD4、CD8、FoxP3、CD20、CD138、CD1a、CD57、CD15、CD117、CD68和CD163。此外,采用组织化学方法鉴定嗜酸性粒细胞。TT患者中CD3⁺和CD4⁺ T细胞的数量高于LL患者。CD8⁺ T细胞在表皮基底层的T淋巴细胞浸润中占主导。不同疾病类型中FoxP3⁺细胞的数量相似,但在BL和LL患者中高于R2个体。TT样本中CD20⁺淋巴细胞最为丰富,而CD138⁺浆细胞无明显差异。TT和R1肉芽肿中心的上皮样巨噬细胞表现为M1表型(CD68⁺CD163⁻),而LL肉芽肿中的巨噬细胞表现为M2表型(CD68⁺CD163⁺)。从TT到LL型疾病,CD1a⁺细胞数量逐渐减少。仅在R2样本中观察到中性粒细胞数量显著增加。除嗜酸性粒细胞外,所有研究的细胞均参与了麻风病的免疫发病机制。