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一种五组分猴痘mRNA疫苗在非人灵长类动物中诱导产生保护性免疫。

A penta-component mpox mRNA vaccine induces protective immunity in nonhuman primates.

作者信息

Ye Qing, Zhang Dong, Zhang Rong-Rong, Xu Qian, Huang Xing-Yao, Huang Baoying, Sun Meng-Xu, Cong Zhe, Zhu Lin, Ma Jianrong, Li Na, Zhang Jingjing, Chen Ting, Lu Jiahan, Hou Yongzhi, Chen Xiang, Liu Hai-Tao, Zhou Chao, Li Rui-Ting, Wu Mei, Wang Zheng-Jian, Yin Jiye, Qiu Ye-Feng, Ying Bo, Tan Wen-Jie, Xue Jing, Qin Cheng-Feng

机构信息

State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, China.

State Key Laboratory of Respiratory Health and Multimorbidity, Beijing Key Laboratory for Animal Models of Emerging and Remerging Infectious Diseases, Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Comparative Medicine Center, Peking Union Medical College, Beijing, China.

出版信息

Nat Commun. 2024 Dec 5;15(1):10611. doi: 10.1038/s41467-024-54909-4.

Abstract

The recent worldwide outbreaks of mpox prioritize the development of a safe and effective mRNA vaccine. The contemporary mpox virus (MPXV) exhibits changing virological and epidemiological features, notably affecting populations already vulnerable to human immunodeficiency virus (HIV). Herein, we profile the immunogenicity of AR-MPXV5, a penta-component mRNA vaccine targeting five specific proteins (M1R, E8L, A29L, A35R, and B6R) from the representative contemporary MPXV clade II strain, in both naive and simian immunodeficiency virus (SIV)-infected nonhuman primates. Immunization with two doses of AR-MPXV5 to cynomolgus macaques effectively elicits antibody responses and cellular responses. Importantly, based on the challenge model with a contemporary MPXV clade II strain, AR-MPXV5 demonstrates effective efficacy in preventing skin lesions, eliminating viremia and reducing viral loads in multiple tissues after challenge in naive male animals. More importantly, AR-MPXV5 is well-tolerated in stable chronic SIV-infected rhesus monkeys, while eliciting comparable MPXV-specific humoral and cellular responses in both naive and SIV-infected monkeys. Together, these results support further clinical development of the AR-MPXV5 vaccine.

摘要

近期猴痘在全球范围内的爆发凸显了研发安全有效的mRNA疫苗的重要性。当代猴痘病毒(MPXV)呈现出不断变化的病毒学和流行病学特征,尤其对已易感染人类免疫缺陷病毒(HIV)的人群产生影响。在此,我们分析了AR-MPXV5的免疫原性,这是一种针对代表性当代MPXV II型毒株的五种特定蛋白(M1R、E8L、A29L、A35R和B6R)的五组分mRNA疫苗,在未感染和感染猿猴免疫缺陷病毒(SIV)的非人灵长类动物中的免疫原性。对食蟹猕猴接种两剂AR-MPXV5可有效引发抗体反应和细胞反应。重要的是,基于当代MPXV II型毒株的攻毒模型,AR-MPXV5在未感染的雄性动物攻毒后,在预防皮肤损伤、消除病毒血症和降低多个组织中的病毒载量方面显示出有效的效力。更重要 的是,AR-MPXV5在稳定的慢性SIV感染的恒河猴中耐受性良好,同时在未感染和SIV感染的猴子中引发相当的MPXV特异性体液和细胞反应。总之,这些结果支持AR-MPXV5疫苗的进一步临床开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd2/11621575/f7813d6e2f92/41467_2024_54909_Fig1_HTML.jpg

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