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针对人畜共患病感染疫苗的“同一健康”佐剂选择

One Health adjuvant selection for vaccines against zoonotic infections.

作者信息

Antipov Anna, Petrovsky Nikolai

机构信息

Vaxine Pty Ltd, Warradale, Adelaide, South Australia 5046, Australia.

Australian Respiratory and Sleep Medicine Institute, Adelaide, South Australia 5042, Australia.

出版信息

Explor Med. 2025;6. doi: 10.37349/emed.2025.1001316. Epub 2025 May 7.


DOI:10.37349/emed.2025.1001316
PMID:40444176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12122014/
Abstract

Vaccines are typically designed either for human or veterinary use. Using One Health principles it would be more efficient to develop a single vaccine to cover all animal and human species at threat from a specific pathogen. A major issue for designing One Health vaccines is that some commonly used human adjuvants such as aluminium salts are not suitable for some animal species, such as felines, where they can cause injection site sarcomas. Conversely, some commonly used animal adjuvants such as mineral oil emulsions are too reactogenic to be used in humans. In addition, species-specific differences in innate immune receptors such as Toll-like receptors (TLR) may mean an adjuvant that works in one species does not work in another. This review presents an overview of human and veterinary adjuvants in use and from this list identifies those that might be most suitable for use in a One Health vaccine strategy. Two notable adjuvant candidates already supported by both human and animal data are squalene oil emulsions and delta inulin-CpG combination adjuvant known as Advax-CpG55.2. These two adjuvants have already been shown to be safe and effective across multiple species including when formulated in influenza vaccines. This could be highly relevant to adjuvant selection for vaccines in development against the current North American bovine H5N1 avian influenza outbreak with the potential need to cover multiple susceptible species including birds, cattle and cats in addition to humans. Additional considerations for One Health adjuvants would be suitable administration routes and dosing across species of widely varying size, physiology and genetics. The availability of adjuvants such as squalene emulsions and Advax-CpG55.2 with broad species activity and safety, including in humans, should make One Health vaccine approaches more common in the future.

摘要

疫苗通常设计用于人类或兽用。运用“同一健康”原则,研发一种单一疫苗以覆盖受特定病原体威胁的所有动物和人类物种会更高效。设计“同一健康”疫苗的一个主要问题是,一些常用的人类佐剂,如铝盐,不适用于某些动物物种,如猫科动物,在猫科动物中它们可能会引发注射部位肉瘤。相反,一些常用的动物佐剂,如矿物油乳剂,对人类来说反应原性太强而不能使用。此外,诸如Toll样受体(TLR)等天然免疫受体的物种特异性差异可能意味着一种在一个物种中起作用的佐剂在另一个物种中不起作用。本综述概述了正在使用的人类和兽用佐剂,并从这份清单中确定了那些可能最适合用于“同一健康”疫苗策略的佐剂。已经得到人类和动物数据支持的两种值得注意的佐剂候选物是角鲨烯油乳剂和名为Advax-CpG55.2的δ-菊粉-CpG组合佐剂。这两种佐剂已被证明在包括流感疫苗配方时在内的多个物种中都是安全有效的。这对于正在研发的针对当前北美牛H5N1禽流感疫情的疫苗的佐剂选择可能高度相关,因为除了人类之外,可能还需要覆盖包括鸟类、牛和猫在内的多个易感物种。“同一健康”佐剂的其他考虑因素将是适合于大小、生理和遗传差异很大的不同物种的给药途径和剂量。角鲨烯乳剂和Advax-CpG55.2等具有广泛物种活性和安全性(包括对人类)的佐剂的可用性,应该会使“同一健康”疫苗方法在未来更普遍。

相似文献

[1]
One Health adjuvant selection for vaccines against zoonotic infections.

Explor Med. 2025

[2]
A phase I study of the safety, reactogenicity and immunogenicity of two quadrivalent seasonal influenza vaccines (Fluzone® or Flublok®) with or without one of two adjuvants (AF03 or Advax-CpG55.2) in healthy adults 18-45 years of age.

Vaccine. 2025-4-30

[3]
An Advax-CpG55.2 adjuvanted recombinant hemagglutinin vaccine provides immunity against H7N9 influenza in adult and neonatal mice.

Vaccine. 2023-8-31

[4]
Developmental and reproductive safety of Advax-CpG55.2™ adjuvanted COVID-19 and influenza vaccines in mice.

Vaccine. 2023-9-22

[5]
Severe acute respiratory syndrome-associated coronavirus vaccines formulated with delta inulin adjuvants provide enhanced protection while ameliorating lung eosinophilic immunopathology.

J Virol. 2015-3

[6]
Combination Adjuvants Enhance Recombinant Protein Vaccine Protection against Fungal Infection.

mBio. 2021-8-31

[7]
Covax-19/Spikogen® vaccine based on recombinant spike protein extracellular domain with Advax-CpG55.2 adjuvant provides single dose protection against SARS-CoV-2 infection in hamsters.

Vaccine. 2022-5-20

[8]
Delta inulin-derived adjuvants that elicit Th1 phenotype following vaccination reduces respiratory syncytial virus lung titers without a reduction in lung immunopathology.

Hum Vaccin Immunother. 2016-8-2

[9]
Advax-SM™-Adjuvanted COBRA (H1/H3) Hemagglutinin Influenza Vaccines.

Vaccines (Basel). 2024-4-24

[10]
Vaccine adjuvant activity of emulsified oils from species of the Pinaceae family.

Phytomedicine. 2019-4-12

本文引用的文献

[1]
A brief history of human infections with H5Ny avian influenza viruses.

Cell Host Microbe. 2025-2-12

[2]
Investigating factors affecting the effectiveness of Gardasil 4, Cervarix, and Gardasil 9 vaccines considering the WHO regions in females: A systematic review.

Cancer Epidemiol. 2025-4

[3]
A population-based study on the burden of hospitalized pediatric pneumococcal disease in Taiwan before and after the introduction of 13-valent pneumococcal conjugate vaccine into the childhood immunization program in 2015.

BMC Infect Dis. 2025-2-5

[4]
Post-marketing safety surveillance for the recombinant zoster vaccine (Shingrix), vaccine adverse event reporting system, United States, October 2017-April 2024.

Prev Med Rep. 2025-1-19

[5]
Persistence of SARS-CoV-2 Antibodies for a Year Following SARS-CoV-2 Vaccinations (BBV152 and ChAdOx1 nCoV-19).

Indian J Clin Biochem. 2025-1

[6]
Globally approved vaccines for COVID-19: a systematic review.

Braz J Microbiol. 2025-3

[7]
Enhancing antibody levels and T cell activity of quadrivalent influenza vaccine by combining it with CpG HP021.

Sci Rep. 2024-12-28

[8]
Serotype distribution of remaining invasive pneumococcal disease after extensive use of ten-valent and 13-valent pneumococcal conjugate vaccines (the PSERENADE project): a global surveillance analysis.

Lancet Infect Dis. 2025-4

[9]
New Dosing Interval and Schedule for the Bexsero MenB-4C Vaccine: Updated Recommendations of the Advisory Committee on Immunization Practices - United States, October 2024.

MMWR Morb Mortal Wkly Rep. 2024-12-12

[10]
Safety and immunogenicity of a SARS-CoV-2 recombinant protein subunit vaccine adjuvanted with Alum + CpG 1018 in healthy Indonesian adults: A multicenter, randomized, comparative, observer-blind, placebo-controlled phase 2 study.

Hum Vaccin Immunother. 2024-12-31

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