Alexander W A, Hartman A B, Oaks E V, Venkatesan M M
Department of Enteric Infections, Walter Reed Army Institute of Research, Washington, DC 20307-5100, USA.
Vaccine. 1996 Aug;14(11):1053-61. doi: 10.1016/0264-410x(96)00002-3.
Human challenge studies with EcSf2a-2, an aroD deletion-attenuated Escherichia coli K12-Shigella flexneri hybrid vaccine expressing S. flexneri 2a somatic antigen and the invasive phenotype indicated that, at doses of 2 x 10(9) bacteria, EcSf2a-2 was immunogenic but also reactogenic and therefore not sufficiently attenuated. Two factors that may contribute to the residual reactogenicity are the spontaneous appearance of plaque-positive variants in the E. coli K12 recipient and the presence of the arg locus encoding enterotoxin or cytotoxin, transferred from S. flexneri 2a into the E. coli recipient. EcSf2a-3 was derived from EcSf2a-2 by introducing a deletion in the virG gene, whose expression is required for plaque formation and keratoconjunctivitis in guinea pigs. EcSf2a-5 contains the same deletion in the E. coli-S. flexneri hybrid strain, 7921, but does not contain the arg locus. Lack of virG expression in these hybrid strains did not affect the immune response to LPS or the development of protective immunity in the guinea pig model.
用EcSf2a - 2进行人体激发试验,EcSf2a - 2是一种aroD缺失减毒的大肠杆菌K12 - 福氏志贺菌杂交疫苗,表达福氏志贺菌2a菌体抗原和侵袭表型,结果表明,在2×10⁹个细菌的剂量下,EcSf2a - 2具有免疫原性,但也有反应原性,因此减毒不足。可能导致残留反应原性的两个因素是大肠杆菌K12受体中噬菌斑阳性变体的自发出现,以及从福氏志贺菌2a转移到大肠杆菌受体中的编码肠毒素或细胞毒素的arg位点的存在。EcSf2a - 3是通过在virG基因中引入缺失而从EcSf2a - 2衍生而来,该基因的表达是豚鼠形成噬菌斑和发生角结膜炎所必需的。EcSf2a - 5在大肠杆菌 - 福氏志贺菌杂交菌株7921中含有相同的缺失,但不含有arg位点。这些杂交菌株中virG表达的缺失并不影响对LPS的免疫反应或豚鼠模型中保护性免疫的发展。