Lobos E, Zahn R, Weiss N, Nutman T B
Department of Medical Parasitology, Swiss Tropical Institute, Basel, Switzerland.
Mol Med. 1996 Nov;2(6):712-24.
Bm2325, a major IgE-inducing antigen of the filarial parasite Brugia malayi has been implicated in the pathology of tropical pulmonary eosinophilia (TPE), a pulmonary syndrome thought to result from hypersensitivity to microfilariae.
Affinity-purified IgE to Bm2325 from patients with TPE was used to identify a complementary DNA (cDNA) from a B. malayi expression library. Sequence analysis of the cDNA revealed a hitherto unknown parasite protein. Immunoblotting of the recombinant filarial protein using sera of patients with TPE determined its IgE-binding capacity. Reactivity to human lung epithelial cell proteins was analyzed using murine anti-Bm2325 antibodies and serum from patients with TPE.
The predicted protein is a homolog of the entire precursor of the gamma-glutamyl transpeptidase (gamma-GT), a key enzyme in the synthesis and degradation of glutathione. The filarial precursor encodes both the heavy (H) and the light (L) chain subunits and shares structural similarities with the mammalian enzymes. The Bm2325 allergen was identified as the homolog of the enzyme light chain subunit. Murine antibodies against the recombinant parasite gamma-GT cross-reacted with the human enzyme present in human airway epithelial cells, and human gamma-GT is a target of antibodies present in the serum of patients with TPE.
Molecular mimicry between the parasite gamma-GT homolog and the host membrane-bound gamma-GT present in lung epithelial cells likely contributes to the pathogenesis observed in tropical pulmonary eosinophilia.
Bm2325是马来布鲁线虫的一种主要诱导IgE的抗原,与热带肺嗜酸性粒细胞增多症(TPE)的病理过程有关,TPE是一种肺部综合征,被认为是由对微丝蚴的超敏反应引起的。
使用从TPE患者中亲和纯化的针对Bm2325的IgE,从马来布鲁线虫表达文库中鉴定互补DNA(cDNA)。对该cDNA的序列分析揭示了一种迄今未知的寄生虫蛋白。使用TPE患者的血清对重组丝虫蛋白进行免疫印迹,以确定其IgE结合能力。使用鼠抗Bm2325抗体和TPE患者的血清分析对人肺上皮细胞蛋白的反应性。
预测的蛋白是γ-谷氨酰转肽酶(γ-GT)整个前体的同源物,γ-GT是谷胱甘肽合成和降解中的关键酶。丝虫前体编码重链(H)和轻链(L)亚基,并且与哺乳动物酶具有结构相似性。Bm2325变应原被鉴定为该酶轻链亚基的同源物。针对重组寄生虫γ-GT的鼠抗体与存在于人气道上皮细胞中的人酶发生交叉反应,并且人γ-GT是TPE患者血清中存在的抗体的靶标。
寄生虫γ-GT同源物与肺上皮细胞中存在的宿主膜结合γ-GT之间的分子模拟可能促成了热带肺嗜酸性粒细胞增多症中观察到的发病机制。