Williams N A
University of Bristol, Department of Pathology and Microbiology, School of Medical Sciences, UK.
Int J Med Microbiol. 2000 Oct;290(4-5):447-53. doi: 10.1016/S1438-4221(00)80062-4.
Cholera toxin (Ctx) and its close relative, Escherichia coli heat-labile enterotoxin (Etx) have long been established as potent mucosal and systemic adjuvants. Problems arising from their inherent toxicity have, however, precluded human use. Here we describe findings which demonstrate that contrary to the established dogma the non-toxic B-subunit of Etx (EtxB) is a highly potent mucosal adjuvant capable of potentiating protective immunity to viral infection. The mechanisms which underlie this activity arise from an ability to trigger specific signaling processes in lymphocyte populations which modulate differentially their activation, differentiation and survival. The elucidation of these properties has led to the further use of EtxB as an agent capable of preventing the establishment of autoimmune diseases. The basis for these activities and their potential applicability to human therapies are discussed.
霍乱毒素(Ctx)及其近亲大肠杆菌不耐热肠毒素(Etx)长期以来一直被确立为强效的黏膜和全身佐剂。然而,因其固有的毒性所引发的问题,使其无法用于人类。在此,我们描述的研究结果表明,与既定的教条相反,Etx的无毒B亚基(EtxB)是一种高效的黏膜佐剂,能够增强对病毒感染的保护性免疫。这种活性背后的机制源于其触发淋巴细胞群体中特定信号传导过程的能力,这些过程会差异性地调节淋巴细胞的激活、分化和存活。对这些特性的阐明促使EtxB进一步被用作预防自身免疫性疾病发生的药物。本文讨论了这些活性的基础及其在人类治疗中的潜在适用性。