Institute of Preventive Medicine, Hyderabad, India.
Vaccine. 2010 May 28;28(24):4086-90. doi: 10.1016/j.vaccine.2010.03.064. Epub 2010 Apr 18.
A chromatographically purified Vero cell rabies vaccine, Indirab manufactured by Bharat Biotech International Limited, Hyderabad, India was subjected to safety and immunogenicity studies by both intramuscular and intradermal routes of administration in parallel with a reference vaccine, Verorab. A Pre-exposure study was undertaken in 239 subjects by intramuscular (IM) route (Study I), Post-exposure study in 188 patients by intramuscular route (Study II) and Simulated post-exposure study in 134 subjects by intradermal (ID) route (Study III). All subjects in these studies were administered with either the test or the reference vaccine as per WHO approved intramuscular and intradermal regimens. The blood samples were collected on days 0, 14 and 35 in case of Study 1, and days 0, 14, 28 and 90 in case of studies II and III. In all studies both vaccine groups had adequate antibody titers (>0.5 IU/mL) on all days tested post-vaccination and there was no significant difference in the titers observed (p>0.05). Some side effects like pain, induration, itching and fever were noted in both vaccine groups in all studies. Both vaccines were well tolerated. Hence it can be concluded that Indirab is as safe and immunogenic as Verorab when administered by both intramuscular and intradermal routes.
印度海得拉巴 Bharat Biotech International 有限公司生产的经色谱纯化的vero 细胞狂犬病疫苗 Indirab ,通过肌肉内和皮内途径与参考疫苗 Verorab 进行了安全性和免疫原性研究。通过肌肉内(IM)途径(研究 I)对 239 名受试者进行了暴露前研究,通过肌肉内途径(研究 II)对 188 名患者进行了暴露后研究,通过皮内(ID)途径(研究 III)对 134 名模拟暴露后患者进行了研究。所有这些研究中的受试者均按照世界卫生组织批准的肌肉内和皮内方案,接受了试验疫苗或参考疫苗的接种。在研究 1 中,所有受试者在第 0、14 和 35 天采血,在研究 2 和 3 中,所有受试者在第 0、14、28 和 90 天采血。在所有研究中,两组疫苗在接种后所有测试日的抗体滴度均足够(>0.5 IU/mL),且观察到的滴度无显著差异(p>0.05)。在所有研究中,两组疫苗均观察到一些副作用,如疼痛、硬结、瘙痒和发热。两种疫苗均具有良好的耐受性。因此,可以得出结论,Indirab 通过肌肉内和皮内途径给药时,与 Verorab 一样安全且具有免疫原性。