一种全细胞百日咳疫苗可降低反应性,保护狒狒免受百日咳挑战。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2024-11-21 Epub Date: 2024-10-23 DOI:10.1128/msphere.00647-24
Parul Kapil, Yihui Wang, Kelsey Gregg, Lindsey Zimmerman, Damaris Molano, Jonatan Maldonado Villeda, Peter Sebo, Tod J Merkel
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引用次数: 0

摘要

20 世纪 40 年代引入的全细胞百日咳(wP)疫苗使百日咳发病率大幅下降,目前仍在全球中低收入国家广泛使用。wP 疫苗的致反应性降低了公众的接受度,这推动了 20 世纪 90 年代无细胞百日咳 (aP) 疫苗在高收入国家的开发和引入。尽管儿科疫苗接种率接近普及,但在引入 aP 疫苗后,高收入国家的百日咳发病率仍有所上升。发病率上升的原因是 aP 疫苗对定植、携带和传播的保护能力降低,而且相对于被其取代的 wP 疫苗,aP 疫苗的免疫持续时间缩短。最近开发出了一种致病反应性降低的全细胞百日咳疫苗(RRwP),其目标是实现与 wP 疫苗相同的保护效果,但安全性有所提高,这可能会使仍在常规使用 wP 疫苗的国家受益。在这项研究中,我们在百日咳狒狒感染模型中测试了 RRwP 疫苗。我们发现,与 wP 疫苗相比,RRwP 疫苗可诱导相似的细胞和体液免疫反应,并在挑战后产生相似的保护作用,同时显著降低了注射部位的致反应性。重要意义世界卫生组织(WHO)于2015年建议,在国家疫苗计划中接种wP疫苗的国家应继续接种wP疫苗,只有在国家免疫计划中能确保和维持定期加强免疫和/或母体免疫接种的情况下,才应考虑改用aP疫苗进行婴儿初次免疫接种(WHO,Vaccine 34:1423-1425,2016,https://doi.org/10.1016/j.vaccine.2015.10.136).由于 aP 疫苗的成本远高于 aP 疫苗,且所需剂量较大,大多数低收入国家仍在使用 wP 疫苗。开发和引入一种可在不牺牲保护作用的前提下减少不良反应的 wP 疫苗将使仍在常规使用 wP 疫苗的国家受益匪浅。本研究的结果表明这一理想目标是可以实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A whole-cell pertussis vaccine engineered to elicit reduced reactogenicity protects baboons against pertussis challenge.

Whole-cell pertussis (wP) vaccines introduced in the 1940s led to a dramatic reduction of pertussis incidence and are still widely used in low- and middle-income countries (LMICs) worldwide. The reactogenicity of wP vaccines resulted in reduced public acceptance, which drove the development and introduction of acellular pertussis (aP) vaccines in high-income countries in the 1990s. Increased incidence of pertussis disease has been observed in high-income countries following the introduction of aP vaccines despite near universal rates of pediatric vaccination. These increases are attributed to the reduced protection against colonization, carriage, and transmission as well as reduced duration of immunity conferred by aP vaccines relative to the wP vaccines they replaced. A reduced reactogenicity whole-cell pertussis (RRwP) vaccine was recently developed with the goal of achieving the same protection as conferred by wP vaccination but with an improved safety profile, which may benefit countries in which wP vaccines are still in routine use. In this study, we tested the RRwP vaccine in a baboon model of pertussis infection. We found that the RRwP vaccine induced comparable cellular and humoral immune responses and comparable protection following challenge relative to the wP vaccine, while significantly reducing injection-site reactogenicity.IMPORTANCEThe World Health Organization (WHO) recommended in 2015 that countries administering wP vaccines in their national vaccine programs should continue to do so, and that switching to aP vaccines for primary infant immunization should only be considered if periodic booster vaccinations and/or maternal immunization could be assured and sustained in their national immunization schedules (WHO, Vaccine 34:1423-1425, 2016, https://doi.org/10.1016/j.vaccine.2015.10.136). Due to the considerably higher cost of aP vaccines and the larger number of doses required, most LMICs continue to use wP vaccines. The development and introduction of a wP vaccine that induces fewer adverse events without sacrificing protection would significantly benefit countries in which wP vaccines are still in routine use. The results of this study indicate this desirable goal may be achievable.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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