One-dose intradermal rabies booster enhances rabies antibody production and avidity maturation.

IF 5.5 3区 医学 Q1 IMMUNOLOGY Medical Microbiology and Immunology Pub Date : 2024-05-18 DOI:10.1007/s00430-024-00791-2
Chidchamai Kewcharoenwong, Saranta Freeouf, Arnone Nithichanon, Wilaiwan Petsophonsakul, Sakorn Pornprasert, Woottichai Khamduang, Tadaki Suzuki, Taishi Onodera, Yoshimasa Takahashi, Ganjana Lertmemongkolchai
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Abstract

The incidence of rabies in Thailand reached its peak in 2018 with 18 human deaths. Preexposure prophylaxis (PrEP) vaccination is thus recommended for high-risk populations. WHO has recently recommended that patients who are exposed to a suspected rabid animal and have already been immunized against rabies should receive a 1-site intradermal (ID) injection of 0.1 mL on days 0 and 3 as postexposure prophylaxis (PEP). In Thailand, village health and livestock volunteers tasked with annual dog vaccination typically receive only a single lifetime PrEP dose and subsequent boosters solely upon confirmed animal bites. However, the adequacy of a single PrEP dose for priming and maintaining immunity in this high-risk group has not been evaluated. Therefore, our study was designed to address two key questions: (1) sufficiency of single-dose PrEP-to determine whether a single ID PrEP dose provides adequate long-term immune protection for high-risk individuals exposed to numerous dogs during their vaccination duties. (2) Booster efficacy for immune maturation-to investigate whether one or two additional ID booster doses effectively stimulate a mature and sustained antibody response in this population. The level and persistence of the rabies antibody were determined by comparing the immunogenicity and booster efficacy among the vaccination groups. Our study demonstrated that rabies antibodies persisted for more than 180 days after cost-effective ID PrEP or the 1st or the 2nd single ID booster dose, and adequate antibody levels were detected in more than 95% of participants by CEE-cELISA and 100% by indirect ELISA. Moreover, the avidity maturation of rabies-specific antibodies occurred after the 1st single ID booster dose. This smaller ID booster regimen was sufficient for producing a sufficient immune response and enhancing the maturation of anti-rabies antibodies. This safe and effective PrEP regimen and a single visit involving a one-dose ID booster are recommended, and at least one one-dose ID booster regimen could be equitably implemented in at-risk people in Thailand and other developing countries. However, an adequate antibody level should be monitored before the booster is administered.

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一剂皮内狂犬病强化剂可增强狂犬病抗体的产生和抗体的成熟。
泰国的狂犬病发病率在 2018 年达到高峰,有 18 人死亡。因此,建议高危人群接种三暴露预防(PrEP)疫苗。世卫组织最近建议,接触过疑似狂犬病动物并已接种狂犬病疫苗的患者,应在第0天和第3天接受一次0.1毫升的皮内注射,作为暴露后预防(PEP)。在泰国,负责每年为狗接种疫苗的乡村卫生和畜牧业志愿者通常只接受一次终生PEP注射,并在确认被动物咬伤后再接受后续加强注射。然而,对这一高风险群体而言,单次 PrEP 剂量是否足以启动和维持免疫力尚未进行过评估。因此,我们的研究旨在解决两个关键问题:(1) 单剂量 PrEP 的充分性--确定单剂量 ID PrEP 是否能为接种疫苗期间接触大量狗的高危人群提供充分的长期免疫保护。(2) 免疫成熟的增效作用--研究一到两次额外的 ID 增效剂量是否能有效刺激该人群产生成熟和持续的抗体反应。通过比较各接种组的免疫原性和强化效果,确定狂犬病抗体的水平和持久性。我们的研究表明,狂犬病抗体在具有成本效益的 ID PrEP 或第 1 或第 2 单次 ID 强化剂量后可持续 180 天以上,95% 以上的参与者通过 CEE-cELISA 检测到了足够的抗体水平,100% 的参与者通过间接 ELISA 检测到了足够的抗体水平。此外,狂犬病特异性抗体在第 1 次单剂 ID 强化治疗后出现了亲和性成熟。这种较小剂量的 ID 强化方案足以产生足够的免疫反应,并促进抗狂犬病抗体的成熟。建议采用这种安全有效的 PrEP 方案和单剂量 ID 强化剂的单次就诊,泰国和其他发展中国家的高危人群可以公平地实施至少单剂量 ID 强化剂方案。不过,在注射加强剂之前,应监测抗体水平是否足够。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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