MVA-85A,一种用于预防儿童和成人结核病的新型候选加强疫苗。

Mark Patrick Nicol, Liesl Anne Grobler
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引用次数: 0

摘要

MVA-85A由牛津紧急结核病联盟有限公司和欧盟资助的研究项目TB- vac共同开发,是一种表达免疫优势型结核(TB)抗原85A的减毒活疫苗,旨在用于异源免疫强化策略来预防结核病。MVA-85A在动物和人类中都具有高度的免疫原性,在卡卡苗接种后或以前暴露于结核病的个体中接种时,可引起强烈的多功能CD4+ t细胞反应。动物研究表明,与单独接种卡介苗相比,先接种卡介苗后接种MVA-85A疫苗的动物有减少病理和细菌负担的趋势;然而,这些积极的影响似乎是有限的,而且由于测试的动物数量少,解释也受到限制。该疫苗在BCG-naïve、以前接种过bcg和结核病暴露的成人以及接种过bcg的青少年和儿童中具有极好的安全性。在本文发表时,MVA-85A正处于比其他新型结核病候选疫苗更高级的临床开发阶段,正在进行大规模的概念验证IIb期临床试验,以确定婴儿结核病的安全性、免疫原性和预防。
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MVA-85A, a novel candidate booster vaccine for the prevention of tuberculosis in children and adults.

MVA-85A, in development by Oxford-Emergent Tuberculosis Consortium Ltd and the EU-funded research program TB-VAC, is a live attenuated viral vaccine expressing the immunodominant tuberculosis (TB) antigen 85A, and is intended for use in a heterologous prime-boost strategy to prevent TB. MVA-85A is highly immunogenic in both animals and humans, eliciting strong polyfunctional CD4+ T-cell responses when administered as a boost following BCG vaccination or when administered to individuals previously exposed to TB. Animal studies have demonstrated trends toward reduced pathology and bacillary burden for animals vaccinated with BCG prime followed by MVA-85A boost compared with BCG alone; however, these positive effects appear to be modest, and interpretation is limited by the small number of animals tested. The vaccine has an excellent safety profile in BCG-naïve, previously BCG-vaccinated and TB-exposed adults, as well as in BCG-vaccinated adolescents and children. At the time of publication, MVA-85A was in a more advanced stage of clinical development than other novel TB vaccine candidates, with a large-scale, proof-of-concept phase IIb clinical trial underway for the determination of safety, immunogenicity and prevention of TB in infants.

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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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