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基于流感病毒载体的TB/FLU-06E疫苗在药物敏感和耐药实验性结核病综合治疗中的应用

TB/FLU-06E Influenza Vector-Based Vaccine in the Complex Therapy of Drug-Susceptible and Drug-Resistant Experimental Tuberculosis.

作者信息

Shurygina Anna-Polina S, Zabolotnykh Natalia V, Vinogradova Tatiana I, Vitovskaya Maria L, Dogonadze Marine Z, Vasilyev Kirill A, Buzitskaya Zhanna V, Yablonskiy Petr K, Lioznov Dmitriy A, Stukova Marina A

机构信息

Smorodintsev Research Institute of Influenza, The Ministry of Health of the Russian Federation, 197022 Saint-Petersburg, Russia.

Saint-Petersburg State Research Institute of Phthisiopulmonology, The Ministry of Health of the Russian Federation, 194064 Saint-Petersburg, Russia.

出版信息

Pharmaceutics. 2024 Jun 25;16(7):857. doi: 10.3390/pharmaceutics16070857.

DOI:10.3390/pharmaceutics16070857
PMID:39065554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11279844/
Abstract

The steady rise of drug-resistant tuberculosis (TB), which renders standard therapy regimens ineffective, necessitates the development of innovative treatment approaches. Immunotherapeutic vaccines have the potential to effectively regulate the anti-TB immune response and enhance the efficacy of anti-TB treatment. In the present study, we aimed to evaluate the potency of the mucosal vector vaccine TB/FLU-06E as part of a complex treatment regimen for drug-susceptible (DS) or drug-resistant (DR) tuberculosis in C57BL/6 mice. Incorporating TB/FLU-06E into the treatment protocol significantly increased the effectiveness of therapy for both forms of tuberculosis. It was evidenced by higher survival rates and reduced pulmonary bacterial load (1.83 lg CFU for DS tuberculosis and 0.93 lg CFU for DR tuberculosis). Furthermore, the treatment reduced pathomorphological lesions in the lungs and stimulated the local and systemic T-helper 1 (Th1) and cytotoxic T-lymphocyte (CTL) anti-TB immune responses. Thus, therapeutic immunization with the TB/FLU-06E vaccine significantly enhances the efficacy of tuberculosis treatment, which is particularly important in DR tuberculosis.

摘要

耐药结核病的持续增加,使标准治疗方案失效,因此需要开发创新的治疗方法。免疫治疗疫苗有潜力有效调节抗结核免疫反应并提高抗结核治疗的疗效。在本研究中,我们旨在评估黏膜载体疫苗TB/FLU-06E作为C57BL/6小鼠对药物敏感(DS)或耐药(DR)结核病综合治疗方案一部分的效力。将TB/FLU-06E纳入治疗方案显著提高了两种形式结核病治疗的有效性。这表现为更高的存活率和降低的肺部细菌载量(DS结核病为1.83 lg CFU,DR结核病为0.93 lg CFU)。此外,该治疗减少了肺部的病理形态学病变,并刺激了局部和全身的辅助性T细胞1(Th1)和细胞毒性T淋巴细胞(CTL)抗结核免疫反应。因此,用TB/FLU-06E疫苗进行治疗性免疫显著提高了结核病治疗的疗效,这在DR结核病中尤为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/70b93ceb00f4/pharmaceutics-16-00857-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/e051fc18bb0a/pharmaceutics-16-00857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/7a57c9fd6ba2/pharmaceutics-16-00857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/f5fdb7a490a2/pharmaceutics-16-00857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/11f2ceff69c4/pharmaceutics-16-00857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/f68ae764d732/pharmaceutics-16-00857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/70b93ceb00f4/pharmaceutics-16-00857-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/e051fc18bb0a/pharmaceutics-16-00857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/7a57c9fd6ba2/pharmaceutics-16-00857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/f5fdb7a490a2/pharmaceutics-16-00857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/11f2ceff69c4/pharmaceutics-16-00857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/f68ae764d732/pharmaceutics-16-00857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d274/11279844/70b93ceb00f4/pharmaceutics-16-00857-g006.jpg

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5
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Front Immunol. 2022 Jun 24;13:878471. doi: 10.3389/fimmu.2022.878471. eCollection 2022.
6
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