课题基金 / 基金详情

NEXT GENERATION VACCINES AGAINST GASTROINTESTINAL MUCOSAL PATHOGENS, USING HELICOBACTER PYLORI AS MODEL PATHOGEN

NEXT GENERATION VACCINES AGAINST GASTROINTESTINAL MUCOSAL PATHOGENS, USING HELICOBACTER PYLORI AS MODEL PATHOGEN
使用幽门螺杆菌作为模型病原体,对抗胃肠粘膜病原体的下一代疫苗
批准号:
10078052
负责人:
金额:
$26.68万
依托单位:
依托单位国家:
英国
项目类别:
EU-Funded
财政年份:
2023
资助国家:
英国
项目状态:
未结题
起止时间:
2023 至 --

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中文摘要
翻译
为了克服危害全球公共健康的抗菌素耐药性(AMR),需要新的策略来开发针对AMR病原体的下一代疫苗。然而,对于发生在粘膜部位的细菌感染,特别是胃肠道的细菌感染,有效疫苗的开发是具有挑战性的。在此背景下,幽门螺杆菌被列为高度优先的AMR病原体和最常见的慢性细菌感染,影响着世界上一半的人口,具有发展为胃癌的高风险。以往幽门螺杆菌疫苗开发方法的失败表明,需要诱导粘膜免疫来保护幽门螺杆菌。因此,Vax2Muc将以直截了当的方式开发针对幽门螺杆菌的合理预防候选药物,并在I期临床试验中直接评估该候选药物的安全性和免疫原性,作为Vax2Muc开发的新疫苗技术的概念验证。为了诱导由组织驻留记忆T细胞维持的长期保护性粘膜免疫反应,我们将应用我们以前识别的疫苗抗原,与有效的佐剂相结合,用于全身启动,并在创新的口腔粘膜膜中实施,以进行粘膜拉动。Vax2Muc将进一步推进GMP的制造,并研究和发展为粘膜应用量身定做的新疫苗技术和策略。我们将在临床前的小鼠和猪模型中评估我们的主要候选方法和替代方法,以确定免疫和保护的有意义的相关性,这对于大多数GI/AMR感染仍然缺乏。因此,Vax2Muc将提供(I)作为PoC的针对幽门螺杆菌的预防性候选疫苗,以及(Ii)丰富的知识和技术,这些知识和技术可以转化为临床开发流程,并广泛适用于各种GI/AMR黏膜病原体,从而显著受益于具有挑战性的黏膜疫苗接种领域,最终减轻AMR/GI疾病的疾病负担。
英文摘要
To overcome antimicrobial resistance (AMR) compromising global public health, novel strategies to develop next generation vaccines against AMR pathogens are required. However, the development of effective vaccines is challenging for bacterial infections occurring at mucosal sites, in particular in the gastrointestinal (GI) tract. In this context, H. pylori is listed as high priority AMR pathogen and the most common chronic bacterial infection affecting half of the world’s population with a high risk to progress into gastric cancer. Previous failures in H. pylori vaccine development approaches suggest that induction of mucosal immunity is required for protection. Thus, Vax2Muc will develop a rational prophylactic lead candidate against H. pylori in a straight-forward manner and directly evaluate this candidate for safety and immunogenicity in a phase I clinical trial, serving as proof-of-concept for novel vaccine technologies developed in Vax2Muc. To induce long-term protective mucosal immune responses sustained by tissue resident memory T cells, we will apply our previously identified vaccine antigens, combined with potent adjuvants for a systemic prime, and implemented in an innovative oro-mucosal film for a mucosal pull. Vax2Muc will further advance GMP manufacturing, and investigate and progress novel vaccine technologies and strategies tailored for mucosal application. We will evaluate our lead candidate and alternative approaches in pre-clinical mouse and pig models to define meaningful correlates of immunity and protection, which are still lacking for most of GI/ AMR infections. Thus, Vax2Muc will deliver (i) a prophylactic vaccine candidate against H. pylori as PoC, and (ii) a wealth of knowledge and technologies that can be translated into the clinical development pipeline and are broadly applicable for various GI/AMR mucosal pathogens to significantly benefit the challenging field of mucosal vaccination and finally reduce disease burden from AMR/GI diseases.
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