van den Akker T W, Naafs B, Kolk A H, De Glopper-van der Veer E, Chin R A, Lien A, Van Joost T
Department of Dermato-Venereology, Academic Hospital Dijkzigt, Rotterdam, The Netherlands.
Br J Dermatol. 1992 Oct;127(4):352-8. doi: 10.1111/j.1365-2133.1992.tb00453.x.
Eight out of 17 mouse anti-Mycobacterium leprae monoclonal antibodies (MAb) were previously observed to react with human nerve and skin antigenic determinants in cryostat sections, using an indirect immunoperoxidase technique. These observations suggested that antigenic mimicry may be involved in the development of the clinical manifestations of leprosy. In the present study we have extended our earlier findings by investigating sera from leprosy patients and MAb using Western blot technique. It was observed that 30 sera and their corresponding F(ab')2 fragments from isolated IgG fractions of both tuberculoid and lepromatous patients reacted with 40-50 epidermal proteins of molecular weights (MW) ranging from 10 to 130 kDa. Sera from 14 controls, however, showed similar reactivity patterns. Absorption of nine patient and control sera with M. tuberculosis, M. marinum and M. kansasii resulted in the removal of several components of different MW in nine, four and three cases, respectively. No consistent differences between sera from leprosy patients and controls were observed. Four out of eight MAb against M. leprae which reacted with determinants in human epidermis and/or dermis in skin cryostat sections reacted with epidermal proteins of MW higher than 39 kDa in Western blot. Four MAb which showed reactivity in cryostat sections did not react in Western blot. Another four MAb did react with human epidermal proteins in Western blot but did not react in cryostat sections, indicating that the MAb were reacting with different epitopes in the two systems. Five MAb did not react with human epidermal proteins either in cryostat sections or in Western blot.(ABSTRACT TRUNCATED AT 250 WORDS)
此前利用间接免疫过氧化物酶技术观察到,17种抗麻风分枝杆菌单克隆抗体(MAb)中有8种可与恒冷箱切片中的人神经和皮肤抗原决定簇发生反应。这些观察结果提示,抗原模拟可能参与了麻风病临床表现的发生发展。在本研究中,我们通过蛋白质免疫印迹技术研究麻风病患者血清和单克隆抗体,扩展了我们早期的研究结果。结果发现,来自结核样型和瘤型患者分离IgG组分的30份血清及其相应的F(ab')2片段,可与分子量(MW)在10至130 kDa范围内的40 - 50种表皮蛋白发生反应。然而,14份对照血清显示出相似的反应模式。用结核分枝杆菌、海分枝杆菌和堪萨斯分枝杆菌分别吸收9份患者和对照血清后,在9例、4例和3例中分别去除了几种不同分子量的成分。未观察到麻风病患者血清与对照血清之间存在一致差异。在皮肤恒冷箱切片中与人类表皮和/或真皮中的决定簇发生反应的8种抗麻风分枝杆菌单克隆抗体中,有4种在蛋白质免疫印迹中与分子量高于39 kDa的表皮蛋白发生反应。4种在恒冷箱切片中显示反应性的单克隆抗体在蛋白质免疫印迹中无反应。另外4种单克隆抗体在蛋白质免疫印迹中与人类表皮蛋白发生反应,但在恒冷箱切片中无反应,这表明单克隆抗体在这两种系统中与不同的表位发生反应。5种单克隆抗体在恒冷箱切片或蛋白质免疫印迹中均不与人类表皮蛋白发生反应。(摘要截取自250词)