Katz David E, DeLorimier Arthur J, Wolf Marcia K, Hall Eric R, Cassels Frederick J, van Hamont John E, Newcomer Rhonda L, Davachi Mitra A, Taylor David N, McQueen Charles E
Department of Enteric Infections, Walter Reed Army Institute of Research (WRAIR), Silver Spring, MD 20910-7500, USA.
Vaccine. 2003 Jan 17;21(5-6):341-6. doi: 10.1016/s0264-410x(02)00613-8.
As a step in the development of an oral vaccine against ETEC, we evaluated the safety and immunogenicity of CS6, a polymeric protein commonly found on the surface of ETEC. Formulations included 1 and 5mg doses of CS6, either encapsulated in biodegradable polymer poly(D, L)-lactide-co-glycolide (PLG), or as free protein, administered orally in a solution of either normal saline or a rice-based buffer. Three doses of CS6 were given at 2-week intervals. Blood was collected immediately before and 7 days after each dose. All formulations were well tolerated. Four of five volunteers who received 1mg CS6 in PLG microspheres with buffer had significant IgA ASC responses (median=30 ASC per 10(6) PBMC) and significant serum IgG responses (median=3.5-fold increase). Oral administration of these prototype ETEC vaccine formulations are safe and can elicit immune responses. The ASC, serum IgA, and serum IgG responses to CS6 are similar in magnitude to the responses after challenge with wild-type ETEC [Coster et al., unpublished data]. Further studies are underway to determine whether these immune responses are sufficient for protection.
作为开发针对肠毒素型大肠杆菌(ETEC)口服疫苗的一个步骤,我们评估了CS6的安全性和免疫原性,CS6是一种常见于ETEC表面的聚合蛋白。制剂包括1毫克和5毫克剂量的CS6,要么封装在可生物降解聚合物聚(D,L)-丙交酯-乙交酯(PLG)中,要么作为游离蛋白,以生理盐水溶液或米基缓冲液口服给药。每隔2周给予三剂CS6。在每次给药前和给药后7天立即采集血液。所有制剂耐受性良好。五名接受含缓冲液的PLG微球中1毫克CS6的志愿者中有四名有显著的IgA ASC反应(中位数=每10⁶个外周血单核细胞中有30个ASC)和显著的血清IgG反应(中位数=增加3.5倍)。口服这些原型ETEC疫苗制剂是安全的,并且可以引发免疫反应。对CS6的ASC、血清IgA和血清IgG反应在程度上与野生型ETEC攻击后的反应相似[科斯特等人,未发表数据]。正在进行进一步研究以确定这些免疫反应是否足以提供保护。