Lehner T
Department of Immunology, United Medical School of Guy's Hospital, London, UK.
Int Rev Immunol. 1997;14(1):21-32. doi: 10.3109/08830189709116842.
Investigation of the aetiology of Behçet's disease (BD) has focused predominantly on herpes simplex virus immunopathology, autoimmunity to oral mucosa or cross-reactive microbial antigens, and streptococcal infection. These aetiological factors might have a common denominator in microbial heat shock protein (HSP) which shows significant homology with the human mitochondrial HSP. Indeed, the uncommon serotypes of Streptococcus sanguis found in BD cross-react with the 65 kD HSP which also shares antigenicity with an oral mucosal antigen. T cell epitope mapping has identified 4 peptides derived from the sequence of the 65 kD HSP which stimulate specifically TCR gamma delta + lymphocytes from patients with BD. These peptides (111-125, 154-172, 219-233 and 311-325) show significant homology with the corresponding peptides derived from the human 60 kD HSP. The specific proliferative response of TCR gamma delta + lymphocytes elicited by the 4 peptides can be used as a laboratory test for the diagnosis of BD. The pathogenic significance of these peptides has been established by inducing uveitis in rats.
白塞病(BD)病因学的研究主要集中在单纯疱疹病毒免疫病理学、针对口腔黏膜的自身免疫或交叉反应性微生物抗原以及链球菌感染。这些病因可能在微生物热休克蛋白(HSP)方面有一个共同的特征,该蛋白与人类线粒体HSP具有显著的同源性。事实上,在BD中发现的罕见血链球菌血清型与65 kD HSP发生交叉反应,而该蛋白也与一种口腔黏膜抗原有共同的抗原性。T细胞表位图谱分析已鉴定出4种源自65 kD HSP序列的肽段,它们可特异性刺激BD患者的TCRγδ +淋巴细胞。这些肽段(111 - 125、154 - 172、219 - 233和311 - 325)与源自人类60 kD HSP的相应肽段具有显著的同源性。这4种肽段引发的TCRγδ +淋巴细胞的特异性增殖反应可作为BD诊断的实验室检测方法。这些肽段的致病意义已通过在大鼠中诱发葡萄膜炎得以证实。