Mpox global health emergency: Insights into the virus, immune responses, and advancements in vaccines PART II: Insights into the advancements in vaccines.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-09-01 DOI:10.12932/AP-111024-1946
Eakachai Prompetchara, Chutitorn Ketloy, Chirayus Khawsang, Tanapat Palaga, Kiat Ruxrungtham
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Abstract

Mpox is currently a global health emergency. This review (Part II) aims to provide insights into Mpox vaccines and their advancements, offering easily digestible information for healthcare workers and researchers. Current Mpox vaccines are all live-attenuated, previously approved for smallpox, and are classified into non-replicating (Modified Vaccinia Ankara-Bavarian Nordic or MVA-BN) and replicating vaccines (Lister clone16m8 KM Biologic or LC16m8KMB and Acambis2000 or ACAM2000). Replicating vaccines offer long-lasting immunity but are contraindicated for immunocompromised individuals and those with extensive dermatitis. Replicating vaccines are administered as a single dose via epicutaneous scarification, while the non-replicating vaccine is given as two subcutaneous doses. Regulatory approvals in various countries are based on animal challenge studies, with limited effectiveness data available. Only LC16m8 is approved for children in Japan, while the others are approved for individuals aged 18 and older. Clinical trials are currently investigating the efficacy and safety of MVA-BN, particularly in children and for post-exposure prophylaxis (PEP). Novel Mpox vaccines that provide cross-protection against orthopoxviruses are needed, with DNA, subunit, and mRNA platforms under development. MPXV-neutralizing antibody-inducing target antigens for vaccine development include the outer envelope antigens of extracellular enveloped virus (EEV): A35R and B6R, and the inner membrane antigens of intracellular mature virus (IMV): M1R, A29L, H3L, and E8L. Two mRNA vaccines are currently in early clinical stages. Importantly, the COVID-19 pandemic underscored the importance of addressing vaccine disparities and improving global access. Transformative approaches are being explored to overcome this challenge and to enhance access in low- and middle-income countries.

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Mpox 全球健康紧急状况:对病毒、免疫反应和疫苗进展的深入研究 第 II 部分:对疫苗进展的深入研究。
麻疹痘目前是全球卫生紧急事件。本综述(第二部分)旨在深入介绍天花疫苗及其进展,为医疗工作者和研究人员提供易于消化的信息。目前的天花疫苗都是减毒活疫苗,以前曾被批准用于治疗天花,分为非复制疫苗(安卡拉-巴伐利亚-北欧改良疫苗或 MVA-BN)和复制疫苗(李斯特克隆 16m8 KM 生物疫苗或 LC16m8KMB 和 Acambis2000 或 ACAM2000)。复制疫苗可提供持久免疫力,但免疫力低下者和患有广泛皮炎者禁用。复制疫苗通过皮外瘢痕注射一次,而非复制疫苗通过皮下注射两次。各国的监管部门是在动物挑战研究的基础上批准的,有效性数据有限。在日本,只有 LC16m8 获准用于儿童,而其他疫苗则获准用于 18 岁及以上人群。目前,临床试验正在调查 MVA-BN 的有效性和安全性,尤其是在儿童和暴露后预防 (PEP) 方面。我们需要能对正痘病毒提供交叉保护的新型 Mpox 疫苗,目前正在开发 DNA、亚单位和 mRNA 平台。用于疫苗开发的 MPXV 中和抗体诱导目标抗原包括细胞外包膜病毒 (EEV) 的外包膜抗原:A35R和B6R,以及细胞内成熟病毒(IMV)的内膜抗原:M1R、A29L、H3L 和 E8L。目前有两种 mRNA 疫苗处于早期临床阶段。重要的是,COVID-19 大流行凸显了解决疫苗差异和改善全球接种的重要性。目前正在探索变革性的方法,以克服这一挑战并提高中低收入国家的可及性。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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