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异基因预激发可逆转免疫衰老,并可能恢复老年人对多种呼吸道病毒的保护作用及疫苗反应性:一项I/II期临床试验的结果

Allo-Priming Reverses Immunosenescence and May Restore Broad Respiratory Viral Protection and Vaccine Responsiveness to the Elderly: Results of a Phase I/II Clinical Trial.

作者信息

Liu Canhui, Yang Xiaochuan, Paoli-Bruno Jorge, Sikes David, Marin-Ruiz Alejandra V, Thomas Nicole, Shane Ryan, Har-Noy Michael

机构信息

Mirror Biologics, Inc., Wesley Chapel, FL 33544, USA.

Coral Research Clinical Corp, Miami, FL 33186, USA.

出版信息

Vaccines (Basel). 2025 Apr 25;13(5):463. doi: 10.3390/vaccines13050463.

Abstract

UNLABELLED

Respiratory viral infections pose a significant health problem that disproportionately affects the elderly. With the aging worldwide population being less responsive to protective vaccines, there is an urgent need for strategies that can protect the elderly from community-acquired viral infections.

BACKGROUND/OBJECTIVES: Allo-priming is a novel immunomodulatory vaccine concept using allogeneic, living, activated Th1 cells that are rejected by the host, creating anti-alloantigen Th1 immunity, increasing Th1 titers. Th1 cells orchestrate cellular immunity, and the age-related decline in Th1 cells contributes to weakened cellular immune response in the elderly, which correlates with poor responsiveness to vaccines and increased susceptibility to respiratory viral infections. Increased Th1 cell titers in the elderly were hypothesized to reverse immunosenescence and restore cellular immune function. Restoration of cellular immune function was predicted to restore broad respiratory viral protection through a heterologous immune mechanism.

METHODS

A phase I/II, multi-center, open-label clinical trial was conducted in 40 healthy adults over 65 years of age to investigate the safety of allo-priming and the effects this vaccination strategy has on cellular immune function over time.

RESULTS

Allo-priming had a benign safety profile and significantly increased the titers of circulating Th1 cells. The increase in Th1 cells was shown to provide broad, self-amplifying respiratory viral protection over time in an ex vivo cytopathic effect assay without additional vaccinations and without any viral antigens included in the formulation, as well acting to increase neutralizing antibody titers in low-responding individuals previously vaccinated for COVID-19.

CONCLUSIONS

These results provide support for an expanded clinical evaluation of this immunomodulatory vaccination strategy as a possible method to restore cellular immune competence to the elderly and provide broad heterologous immune protection from respiratory viral infections without the need for frequent vaccine re-formulations or booster shots (National Library of Medicine: NCT04441047).

摘要

未标注

呼吸道病毒感染是一个严重的健康问题,对老年人的影响尤为严重。随着全球人口老龄化,人们对保护性疫苗的反应性降低,迫切需要采取策略来保护老年人免受社区获得性病毒感染。

背景/目的:异基因启动是一种新型免疫调节疫苗概念,使用被宿主排斥的同种异体活活化Th1细胞,产生抗同种异体抗原Th1免疫,提高Th1细胞滴度。Th1细胞协调细胞免疫,与年龄相关的Th1细胞减少导致老年人细胞免疫反应减弱,这与疫苗反应性差和呼吸道病毒感染易感性增加相关。假设提高老年人的Th1细胞滴度可逆转免疫衰老并恢复细胞免疫功能。预计细胞免疫功能的恢复将通过异源免疫机制恢复广泛的呼吸道病毒保护。

方法

在40名65岁以上的健康成年人中进行了一项I/II期多中心开放标签临床试验,以研究异基因启动的安全性以及这种疫苗接种策略随时间对细胞免疫功能的影响。

结果

异基因启动具有良好的安全性,显著提高了循环Th1细胞的滴度。在体外细胞病变效应试验中,随着时间的推移,Th1细胞的增加显示出可提供广泛的、自我增强的呼吸道病毒保护,无需额外接种疫苗,制剂中也不包含任何病毒抗原,并且还可提高先前接种过COVID-19疫苗的低反应个体的中和抗体滴度。

结论

这些结果为扩大对这种免疫调节疫苗接种策略的临床评估提供了支持,该策略可能是一种恢复老年人细胞免疫能力的方法,并提供广泛的异源免疫保护,免受呼吸道病毒感染,而无需频繁重新配制疫苗或加强注射(美国国立医学图书馆:NCT04441047)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ab5/12115621/b26ebfe694ad/vaccines-13-00463-g001.jpg

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