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Extending the Breadth of Influenza Vaccines: Status and Prospects for a Universal Vaccine

机译:延长流感疫苗的宽度:通用疫苗的地位和前景

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摘要

Despite the widespread use of seasonal influenza vaccines, there is urgent need for a universal influenza vaccine to provide broad, long-term protection. A number of factors underpin this urgency, including threats posed by zoonotic and pandemic influenza A viruses, suboptimal effectiveness of seasonal influenza vaccines, and concerns surrounding the effects of annual vaccination. In this article, we discuss approaches that are being investigated to increase influenza vaccine breadth, which are near-term, readily achievable approaches to increase the range of strains recognized within a subtype, or longer-term more challenging approaches to produce a truly universal influenza vaccine. Adjuvanted and neuraminidase-optimized vaccines are emerging as the most feasible and promising approaches to extend protection to cover a broader range of strains within a subtype. The goal of developing a universal vaccine has also been advanced with the design of immunogenic influenza HA-stem constructs that induce broadly neutralizing antibodies. However, these constructs are not yet sufficiently immunogenic to induce lasting universal immunity in humans. Advances in understanding how T cells mediate protection, and how viruses are packaged, have facilitated the rationale design and delivery of replication-incompetent virus vaccines that induce broad protection mediated by lung-resident memory T cells. While the lack of clear mechanistic correlates of protection, other than haemagglutination-inhibiting antibodies, remains an impediment to further advancing novel influenza vaccines, the pressing need for such a vaccine is supporting development of highly innovative and effective strategies.
机译:尽管季节性流感疫苗被广泛使用,但迫切需要一种通用流感疫苗来提供广泛、长期的保护。许多因素支持了这一紧迫性,包括人畜共患病和大流行性甲型流感病毒构成的威胁、季节性流感疫苗的效果不佳,以及围绕年度疫苗接种效果的担忧。在这篇文章中,我们讨论了正在研究的增加流感疫苗广度的方法,这些方法是短期的、易于实现的、增加亚型内识别菌株范围的方法,或者是生产真正通用流感疫苗的更具挑战性的长期方法。佐剂疫苗和神经氨酸酶优化疫苗正在成为最可行和最有希望的方法,以扩大保护范围,覆盖亚型中更广泛的菌株。随着免疫原性流感HA干细胞结构的设计,开发通用疫苗的目标也得到了推进,该结构可诱导广泛中和的抗体。然而,这些结构还没有足够的免疫原性来诱导人类持久的普遍免疫。在了解T细胞如何介导保护以及病毒如何包装方面取得的进展,有助于设计和提供复制功能不全的病毒疫苗,该疫苗可诱导肺驻留记忆T细胞介导的广泛保护。尽管除了抑制血凝素的抗体外,缺乏明确的保护机制相关因素仍然是进一步开发新型流感疫苗的障碍,但对这种疫苗的迫切需求正在支持开发高度创新和有效的策略。

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