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口服亚单位疫苗设计的进展

Advances in Oral Subunit Vaccine Design.

作者信息

Van der Weken Hans, Cox Eric, Devriendt Bert

机构信息

Department of Virology, Parasitology and Immunology, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.

出版信息

Vaccines (Basel). 2020 Dec 22;9(1):1. doi: 10.3390/vaccines9010001.

Abstract

Many pathogens invade the host at the intestinal surface. To protect against these enteropathogens, the induction of intestinal secretory IgA (SIgA) responses is paramount. While systemic vaccination provides strong systemic immune responses, oral vaccination is the most efficient way to trigger protective SIgA responses. However, the development of oral vaccines, especially oral subunit vaccines, is challenging due to mechanisms inherent to the gut. Oral vaccines need to survive the harsh environment in the gastrointestinal tract, characterized by low pH and intestinal proteases and need to reach the gut-associated lymphoid tissues, which are protected by chemical and physical barriers that prevent efficient uptake. Furthermore, they need to surmount default tolerogenic responses present in the gut, resulting in suppression of immunity or tolerance. Several strategies have been developed to tackle these hurdles, such as delivery systems that protect vaccine antigens from degradation, strong mucosal adjuvants that induce robust immune responses and targeting approaches that aim to selectively deliver vaccine antigens towards specific immune cell populations. In this review, we discuss recent advances in oral vaccine design to enable the induction of robust gut immunity and highlight that the development of next generation oral subunit vaccines will require approaches that combines these solutions.

摘要

许多病原体在肠道表面侵入宿主。为抵御这些肠道病原体,诱导肠道分泌型IgA(SIgA)反应至关重要。虽然全身疫苗接种可提供强大的全身免疫反应,但口服疫苗接种是触发保护性SIgA反应的最有效方式。然而,由于肠道固有的机制,口服疫苗尤其是口服亚单位疫苗的研发具有挑战性。口服疫苗需要在胃肠道的恶劣环境中存活下来,这种环境的特点是低pH值和肠道蛋白酶,并且需要到达肠道相关淋巴组织,这些组织受到化学和物理屏障的保护,会阻碍有效摄取。此外,它们还需要克服肠道中存在的默认致耐受性反应,从而导致免疫抑制或耐受。已经开发了几种策略来克服这些障碍,例如保护疫苗抗原不被降解的递送系统、诱导强烈免疫反应的强效黏膜佐剂以及旨在将疫苗抗原选择性递送至特定免疫细胞群体的靶向方法。在这篇综述中,我们讨论了口服疫苗设计方面的最新进展,以实现强大的肠道免疫诱导,并强调下一代口服亚单位疫苗的开发将需要结合这些解决方案的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fcb/7822154/b9bc12aa8cbf/vaccines-09-00001-g001.jpg

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