首页|重组B群脑膜炎球菌疫苗大鼠安全性和免疫原性研究

重组B群脑膜炎球菌疫苗大鼠安全性和免疫原性研究

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目的 对大鼠重复给予重组B群脑膜炎球菌疫苗,考察该创新疫苗的非临床安全性和免疫原性,为临床设计人用剂量及临床毒副反应的监测提供参考依据.方法 使用SD大鼠,设计阴性对照组、佐剂对照组、疫苗低剂量组(每只1剂)和高剂量组(每只3剂)4个主试验组及3个卫星组.于第0、3、6、9、12周分别肌肉注射,进行临床观察和解剖观察,并对多种组织脏器进行病理学检查.检测体质量、食量、体温、血细胞计数、凝血功能、血液生化、眼科、T淋巴细胞亚群、细胞因子、血清特异性IgG抗体和杀菌抗体等指标.结果 低、高剂量重组B群脑膜炎球菌疫苗均能产生高水平的结合抗体,免疫血清具有较强活性的杀菌抗体.低、高剂量组疫苗可引起大鼠中性粒细胞、单核细胞及淋巴细胞显著升高,血红蛋白和红细胞比容显著降低.与给药相关的改变还表现为血清球蛋白升高,白蛋白降低,与之伴随的A/G值降低.4周恢复期后均可恢复正常.与佐剂和疫苗免疫相关的组织病理学改变为注射局部可见轻微至中度肉芽肿性炎症、急性炎症,坐骨神经外膜单个核细胞/混合细胞浸润、增生,淋巴结髓索浆细胞数目及粒细胞系增多等.结论 重组B群脑膜炎球菌疫苗对SD大鼠具有良好的免疫原性和安全性,未见免疫毒性反应,可见与铝佐剂和免疫反应相关的外周血液指标变化以及注射部位炎症.本试验剂量下,重组B群脑膜炎球菌疫苗未见不良反应剂量(no observed adverse effect level,NOAEL)为每只3剂.
Safety and Immunogenicity of Recombinant Group B Meningococcal Vaccine in Rats
OBJECTIVE To investigate the non-clinical safety and immunogenicity of recombinant group B meningococcal vac-cine by repeatedly dose to rats,so as to provide reference for designing dose level and monitoring toxicity and side effects in clinical tri-als.METHODS SD rats were used to design 4 main toxicity groups including negative control group,adjuvant control group,low dose vaccine group(1 dose each)and high dose vaccine group(3 doses each)and 3 satellite groups.The vaccine was dosed by intra-muscular injection at weeks 0,3,6,9 and 12 respectively.During the study,all the animals of the main toxicity group were observed for clinical signs,indicators such as body weights,food consumption,body temperature,blood cells counting,coagulation,serum bio-chemistry,ophthalmology,T lymphocyte subsets and cytokines were detected.Serum specific IgG antibody and bactericidal antibody were measured for satellite animals.All the animals were observed anatomically,main organs were weighed to the calculate viscera/body ratio and the viscera/brain ratio,and various tissues and organs were examined pathologically.RESULTS It could produce high-leveled binding antibodies and bactericidal antibodies with strong activity in immune serum that rats injected the low and high do-ses of recombinant group B meningococcal vaccines.Both the low and high dose vaccines caused the increases in neutrophils,mono-cytes and lymphocytes significantly,the decreases in hemoglobin and RBC significantly.Other dose-related changes involved the in-crease in serum globulin and decrease in albumin,with concomitant decrease in A/G,which basically returned to normal after 4 weeks of recovery period.The histopathological findings associated with adjuvant and vaccine were mild or moderate granulomatous inflamma-tion,acute inflammation in injection site,infiltration and proliferation of mononuclear cells/mixed cells in the sciatic membrane,and increased number of myeloid plasma cells and granulocytes in lymph nodes.CONCLUSION Recombinant group B meningococcal vaccine had good immunogenicity and safety profile in SD rats,there is no immune toxicity reaction.It is obvious that adjuvant and vaccine-related changes in indicators of peripheral blood and the inflammation response in injection site.Under the dose levels of this study,there is no adverse effect level on recombinant B group meningococcal vaccine for 3 doses/one rat.

recombinant group B meningococcal vaccineratimmunogenicitysafety

苏桂民、纪国存、郭通、冀颖、龙静、王欣惠、朱卫华、杜琳

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北京市细菌性疫苗工程技术研究中心,北京 100176

北京智飞绿竹生物制药有限公司研发中心,北京 100176

重组B群脑膜炎球菌疫苗 大鼠 免疫原性 安全性

2024

中国药学杂志
中国药学会

中国药学杂志

CSTPCD北大核心
影响因子:0.957
ISSN:1001-2494
年,卷(期):2024.59(2)
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