U.S. Naval Medical Research Unit No. 6 (NAMRU-6), Callao, Peru.
Infect Immun. 2014 May;82(5):2027-36. doi: 10.1128/IAI.01665-13. Epub 2014 Mar 4.
Several animal models exist to evaluate the immunogenicity and protective efficacy of candidate Shigella vaccines. The two most widely used nonprimate models for vaccine development include a murine pulmonary challenge model and a guinea pig keratoconjunctivitis model. Nonhuman primate models exhibit clinical features and gross and microscopic colonic lesions that mimic those induced in human shigellosis. Challenge models for enterotoxigenic Escherichia coli (ETEC) and Campylobacter spp. have been successfully developed with Aotus nancymaae, and the addition of a Shigella-Aotus challenge model would facilitate the testing of combination vaccines. A series of experiments were designed to identify the dose of Shigella flexneri 2a strain 2457T that induces an attack rate of 75% in the Aotus monkey. After primary challenge, the dose required to induce an attack rate of 75% was calculated to be 1 × 10(11) CFU. Shigella-specific immune responses were low after primary challenge and subsequently boosted upon rechallenge. However, preexisting immunity derived from the primary challenge was insufficient to protect against the homologous Shigella serotype. A successive study in A. nancymaae evaluated the ability of multiple oral immunizations with live-attenuated Shigella vaccine strain SC602 to protect against challenge. After three oral immunizations, animals were challenged with S. flexneri 2a 2457T. A 70% attack rate was demonstrated in control animals, whereas animals immunized with vaccine strain SC602 were protected from challenge (efficacy of 80%; P = 0.05). The overall study results indicate that the Shigella-Aotus nancymaae challenge model may be a valuable tool for evaluating vaccine efficacy and investigating immune correlates of protection.
存在几种动物模型可用于评估候选志贺氏菌疫苗的免疫原性和保护效力。两种最广泛用于疫苗开发的非灵长类动物模型包括鼠类肺部攻毒模型和豚鼠角膜结膜炎模型。非人类灵长类动物模型表现出的临床特征和大体及显微镜下的结肠病变与人类志贺氏菌病诱导的病变相似。已经成功地使用南迪猕猴建立了肠产毒性大肠杆菌(ETEC)和弯曲菌属挑战模型,添加志贺氏菌-南迪猕猴挑战模型将有助于测试联合疫苗。设计了一系列实验来确定诱导南迪猕猴攻击率为 75%的福氏志贺氏菌 2a 株 2457T 的剂量。初次攻毒后,计算出诱导攻击率为 75%所需的剂量为 1×10(11)CFU。初次攻毒后志贺氏菌特异性免疫反应较低,随后再攻毒时增强。然而,初次攻毒产生的固有免疫力不足以保护免受同源志贺氏菌血清型的攻击。南迪猕猴中的一项后续研究评估了多次口服免疫活减毒志贺氏菌疫苗株 SC602 以抵抗攻毒的能力。经过三次口服免疫后,用福氏志贺氏菌 2a 2457T 对动物进行攻毒。对照组动物的攻击率为 70%,而用疫苗株 SC602 免疫的动物则受到保护而免受攻毒(效力为 80%;P=0.05)。总的研究结果表明,志贺氏菌-南迪猕猴攻毒模型可能是评估疫苗效力和研究保护免疫相关性的有用工具。