Jelinek Tomas, Schunk Mirjam, Reisinger Emil C, Addo Marylyn M, Wiedermann Ursula, Costantini Marco, Lattanzi Maria, Pellegrini Michele, Galgani Ilaria
Berlin Center for Travel and Tropical Medicine, Berlin, Germany.
Institute of Infectious Diseases and Tropical Medicine, LMU Klinikum, Munich, Germany.
PLoS Negl Trop Dis. 2025 May 27;19(5):e0013118. doi: 10.1371/journal.pntd.0013118. eCollection 2025 May.
Rabies pre-exposure prophylaxis (PrEP) is recommended to individuals at risk for exposure to rabies. Three intramuscular doses of the purified chick embryo cell (PCEC) rabies vaccine can be administered according to a conventional (four-week) or an accelerated (one-week) regimen.
METHODOLOGY/PRINCIPAL FINDINGS: This phase III, open-label study (NCT02545517) was an extension of the NCT01662440 study where immune responses of different primary PrEP regimens with PCEC rabies vaccine and Japanese encephalitis (JE) vaccine were assessed. Adults who had completed the parent study and received three doses of rabies PrEP regimens, concomitantly with a JE vaccine or alone (i.e., Rabies+JE-Accelerated, Rabies+JE-Conventional, and Rabies-Conventional groups) were enrolled in this extension study. Here we evaluated the long-term (up to 10 years after completing the primary vaccination) immunogenicity and boostability of PCEC rabies vaccine, and the safety of booster dose(s). Immunogenicity was assessed in terms of rabies virus neutralizing antibody (RVNA) concentrations, and titers ≥0.5 international units (IU)/mL were considered adequate for protection. Participants with RVNA concentrations <0.5 IU/mL were eligible for receiving PCEC rabies vaccine booster(s). Of the 459 participants enrolled in this study, 77.6% completed the trial. At the study end, the probability of detecting adequate RVNA concentrations in unboosted participants was 57.8%, 60.2%, and 62.0% for the Rabies+JE-Accelerated, Rabies+JE-Conventional, and Rabies-Conventional groups, respectively. Overall, 68.6% of all participants had RVNA concentrations ≥0.5 IU/mL at any timepoint and did not require a booster dose during the study follow-up period. Of the 144 participants with RVNA concentrations <0.5 IU/mL at any timepoint, 132 needed one booster dose throughout the follow-up period (Years 3-10) and 12 needed multiple booster administrations. No safety concerns were identified.
CONCLUSION/SIGNIFICANCE: The PCEC rabies vaccine administered alone/concomitantly with the JE vaccine provides adequate immunity for up to 62% of unboosted participants at study end.
建议对有狂犬病暴露风险的个体进行狂犬病暴露前预防(PrEP)。可按照常规(四周)或加速(一周)方案接种三剂肌内注射的纯化鸡胚细胞(PCEC)狂犬病疫苗。
方法/主要发现:这项III期开放标签研究(NCT02545517)是NCT01662440研究的扩展,在NCT01662440研究中评估了PCEC狂犬病疫苗和日本脑炎(JE)疫苗不同初次PrEP方案的免疫反应。完成母研究并接受三剂狂犬病PrEP方案、同时接种JE疫苗或单独接种(即狂犬病+JE-加速组、狂犬病+JE-常规组和狂犬病-常规组)的成年人被纳入这项扩展研究。在此,我们评估了PCEC狂犬病疫苗的长期(初次接种完成后长达10年)免疫原性和可增强性,以及加强剂量的安全性。根据狂犬病病毒中和抗体(RVNA)浓度评估免疫原性,滴度≥0.5国际单位(IU)/mL被认为足以提供保护。RVNA浓度<0.5 IU/mL的参与者有资格接受PCEC狂犬病疫苗加强针。在这项研究纳入的459名参与者中,77.6%完成了试验。在研究结束时,狂犬病+JE-加速组、狂犬病+JE-常规组和狂犬病-常规组未加强的参与者中检测到足够RVNA浓度的概率分别为57.8%、60.2%和62.0%。总体而言,68.6%的所有参与者在任何时间点的RVNA浓度≥0.5 IU/mL,并且在研究随访期间不需要加强剂量。在任何时间点RVNA浓度<0.5 IU/mL的144名参与者中,132名在整个随访期(第3 - 10年)需要一剂加强针,12名需要多次加强接种。未发现安全问题。
结论/意义:单独/与JE疫苗同时接种的PCEC狂犬病疫苗在研究结束时为高达62%的未加强参与者提供了足够的免疫力。