Clark H F, Offit P A, Ellis R W, Eiden J J, Krah D, Shaw A R, Pichichero M, Treanor J J, Borian F E, Bell L M, Plotkin S A
Department of Pediatrics, School of Medicine, University of Pennsylvania, Philadelphia, USA.
J Infect Dis. 1996 Sep;174 Suppl 1:S73-80. doi: 10.1093/infdis/174.supplement_1.s73.
Laboratory and clinical studies have been directed toward development of a vaccine against rotavirus gastroenteritis in infants. First, bovine rotavirus strain WC3, which did not induce neutralizing antibodies to predominant human rotavirus (HRV) serotypes, was determined to be safe and immunogenic; however, it was not protective in all efficacy trials. HRVs adapted to cell culture retained some virulence for infants, but when further attenuated by cold adaptation, they were poorly immunogenic. Reassortant rotaviruses were designed to express HRV surface proteins VP7 (G) or VP4 (P) while retaining a bovine WC3 genome background. Reassortants containing either HRV surface protein and as few as four bovine rotavirus genes were safe in infants. A monovalent WC3 reassortant of serotype G1 specificity was 64%-100% protective in placebo-controlled trials. A quadrivalent WC3 reassortant vaccine with components of HRV G1, G2, G3, and P[8] specificity induced 67% protection against all rotavirus disease in a multicenter efficacy trial.
实验室和临床研究一直致力于研发针对婴儿轮状病毒肠胃炎的疫苗。首先,牛轮状病毒WC3株虽不能诱导针对主要人类轮状病毒(HRV)血清型的中和抗体,但被确定为安全且具有免疫原性;然而,在所有效力试验中它都没有保护作用。适应细胞培养的HRV对婴儿仍有一定毒力,但经冷适应进一步减毒后,其免疫原性较差。重配轮状病毒被设计为表达HRV表面蛋白VP7(G)或VP4(P),同时保留牛WC3基因组背景。含有任一HRV表面蛋白且仅有四个牛轮状病毒基因的重配病毒对婴儿是安全的。在安慰剂对照试验中,G1血清型的单价WC3重配病毒具有64% - 100%的保护作用。一种具有HRV G1、G2、G3和P[8]特异性成分的四价WC3重配疫苗在一项多中心效力试验中对所有轮状病毒疾病诱导了67%的保护作用。