Chugh I B, Khuller G K
Dept of Biochemistry, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Eur Respir J. 1993 Jun;6(6):811-5.
We wanted to determine the immunoprotective behaviour of cell wall protein peptidoglycan complex (CW-PPC) of Mycobacterium tuberculosis H37Ra, using liposomes as adjuvant, in an experimental animal model. Immunization of mice with CW-PPC entrapped in liposomes induced both humoral response, as measured by enzyme-linked immunosorbent assay (ELISA), and cell-mediated immune responses, as seen by delayed type hypersensitivity (DTH) and leucocyte migration inhibition (LMI) techniques. Ten days after complete immunization, the animals were challenged with median lethal dose (LD50) of M. tuberculosis H37Rv. The animals exhibited significant protection, as evident by 72% survival after 30 days of infection, compared to 38% survival in control animals. Protective effect of immunization with liposome entrapped CW-PPC was further substantiated by significant decrease in the number of viable bacilli in lungs, liver and spleen of immunized animals, as compared to control animals. These results indicate that immunization with liposome-entrapped mycobacterial cell wall protein peptidoglycan complex induces protection against experimental tuberculosis.
我们希望在实验动物模型中,以脂质体作为佐剂,确定结核分枝杆菌H37Ra的细胞壁蛋白肽聚糖复合物(CW-PPC)的免疫保护行为。用包封于脂质体中的CW-PPC免疫小鼠,通过酶联免疫吸附测定(ELISA)检测到体液免疫反应,通过迟发型超敏反应(DTH)和白细胞迁移抑制(LMI)技术观察到细胞介导的免疫反应。完全免疫后10天,用结核分枝杆菌H37Rv的半数致死剂量(LD50)攻击动物。与对照动物38%的存活率相比,感染30天后72%的存活率表明动物表现出显著的保护作用。与对照动物相比,免疫动物肺、肝和脾中活菌数量显著减少,进一步证实了用包封于脂质体中的CW-PPC免疫的保护作用。这些结果表明,用包封于脂质体中的分枝杆菌细胞壁蛋白肽聚糖复合物免疫可诱导对实验性结核病的保护作用。