Gupta R K, Anderson R, Cecchini D, Rost B, Griffin P, Benscoter K, Xu J, Montanez-Ortiz L, Siber G R
Massachusetts Public Health Biologic Laboratories, State Laboratory Institute Boston, USA.
Dev Biol Stand. 1996;86:283-96.
We have evaluated a guinea pig model for assessing the immunogenicity of Haemophilus influenzae type b (Hib) polysaccharide-protein conjugate vaccines, acellular pertussis vaccine and combination vaccines-consisting of tetanus toxoid (TT), diphtheria toxoid (DT), acellular pertussis vaccine and Hib-TT (Hib-T) conjugate vaccine. The model was based on the United States (US) potency test for TT and DT which requires injection of guinea pigs with a single dose of undiluted vaccine. Guinea pigs showed dose-dependent antibody responses to pertussis toxoid (PTxd) and filamentous haemagglutinin (FHA), two important components of acellular pertussis vaccine. Antibody response of guinea pigs to commercially available Hib conjugate vaccines qualitatively resembled those of human infants. Unconjugated polyribosylribitolphosphate (PRP) was not immunogenic; PRP-D conjugate produced a low antibody response, HbOC, PRP-T (Merieux) and Hib-T (MPHBL) produced a low response to the first dose and a strong anamnestic response to the booster dose. PRP-OMP uniquely produced a strong response after the first dose which was boosted by the second dose. In preliminary experiments, injection of guinea pigs with the combined vaccine formulations consisting of TT, DT, whole cell or acellular pertussis vaccine (Ptxd and FHA) and Hib-T conjugate showed that these vaccines were immunogenic when combined, with some effects on the antibody responses of certain components. This model for testing potency/immunogenicity of combined vaccines substantially reduces the number of animals needed to test each lot of vaccine. To reduce the use of animals in testing vaccines further, we propose the use of a Vero cell assay for titrating diphtheria antitoxin and ELISA for measuring IgG antibody to tetanus toxin. The guinea pig model may also be useful for evaluating combination vaccines.
我们评估了一种豚鼠模型,用于评估b型流感嗜血杆菌(Hib)多糖蛋白结合疫苗、无细胞百日咳疫苗以及由破伤风类毒素(TT)、白喉类毒素(DT)、无细胞百日咳疫苗和Hib-TT(Hib-T)结合疫苗组成的联合疫苗的免疫原性。该模型基于美国对TT和DT的效力测试,该测试要求给豚鼠注射单剂量未稀释的疫苗。豚鼠对无细胞百日咳疫苗的两个重要成分百日咳毒素(PTxd)和丝状血凝素(FHA)表现出剂量依赖性抗体反应。豚鼠对市售Hib结合疫苗的抗体反应在质量上与人类婴儿相似。未结合的多聚核糖基核糖醇磷酸酯(PRP)无免疫原性;PRP-D结合物产生低抗体反应,HbOC、PRP-T(梅里埃公司)和Hib-T(MPHBL)对首剂产生低反应,对加强剂量产生强烈的回忆反应。PRP-OMP在首剂后独特地产生强烈反应,并在第二剂后增强。在初步实验中,给豚鼠注射由TT、DT、全细胞或无细胞百日咳疫苗(Ptxd和FHA)以及Hib-T结合物组成的联合疫苗制剂,结果表明这些疫苗联合使用时具有免疫原性,对某些成分的抗体反应有一些影响。这种用于测试联合疫苗效力/免疫原性的模型大大减少了测试每批疫苗所需的动物数量。为了进一步减少疫苗测试中动物的使用,我们建议使用Vero细胞测定法滴定白喉抗毒素,并使用酶联免疫吸附测定法测量破伤风毒素的IgG抗体。豚鼠模型也可能有助于评估联合疫苗。