Evaluation and comparison of immune responses induced by two Mpox mRNA vaccine candidates in mice

免疫系统 牛痘 病毒学 抗原 病毒 抗体 生物 中和抗体 信使核糖核酸 免疫学 重组DNA 基因 生物化学
作者
Xidan Yang,Congxia Hu,Xuetao Yang,Xiu Yang,Xing Hu,Xingyun Wang,Cong Liu,Yuan Yuan,Shouwen Du,Peng George Wang,Jihui Lin
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:95 (10) 被引量:13
标识
DOI:10.1002/jmv.29140
摘要

The epidemic of Mpox virus (MPXV) from May 2022 was once declared as a Public Health Emergency of International Concern by the World Health Organization. Vaccines play an important role in prevention of infectious diseases, and mRNA vaccine technology was proved to be a safe and effective platform with successful application in defense of coronavirus disease 2019. In this study, based on A29L, M1R, A35R, and B6R of MPXV, we developed two MPXV mRNA vaccine candidates, designated as MPXfus and MPXmix. The MPXfus was one-component, in which these four antigen proteins were linked in tandem by flexible linker and encoded by an individual mRNA as a fusion protein. The MPXmix was multicomponent containing four mRNA, and each mRNA encoded one antigen protein respectively. Mice were immunized with equal quality of MPXfus or MPXmix, delivered by lipid nanoparticles for evaluation and comparison of the immune responses induced by these two MPXV vaccine candidates. Results of immune response analyses indicated that both MPXfus and MPXmix could elicit high-level of antigen-specific antibodies and robust cellular immune response in mice. Moreover, results of virus neutralization assays suggested that sera from MPXfus- or MPXmix-immunized mice possessed high neutralizing activities against vaccinia virus. In addition, titers of antigen-specific antibody, levels of cellular immune response, and activities of neutralizing antibody against vaccinia virus induced by MPXfus and MPXmix presented no significant difference. In summary, this study provides valuable insights for further clinical development of one-component and multicomponent mRNA vaccine candidates for the prevention of MPXV and other orthomyxoviruses.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
aibiotech完成签到,获得积分10
1秒前
2秒前
汉堡包应助hulala采纳,获得10
3秒前
寒冷的迎南完成签到,获得积分10
3秒前
LLL完成签到,获得积分10
7秒前
Ava应助科研通管家采纳,获得10
7秒前
所所应助科研通管家采纳,获得10
7秒前
Owen应助科研通管家采纳,获得10
7秒前
机灵柚子应助科研通管家采纳,获得20
7秒前
乐乐应助科研通管家采纳,获得10
8秒前
9秒前
土豆发布了新的文献求助10
9秒前
10秒前
李健应助boltos采纳,获得10
10秒前
lizhiqian2024发布了新的文献求助10
12秒前
爱笑西牛完成签到,获得积分10
13秒前
hc完成签到 ,获得积分10
13秒前
14秒前
baolongzhan完成签到,获得积分10
16秒前
hulala发布了新的文献求助10
16秒前
爱笑西牛发布了新的文献求助10
16秒前
monan发布了新的文献求助10
16秒前
清脆又晴完成签到,获得积分10
16秒前
不知道完成签到,获得积分10
17秒前
羲月完成签到,获得积分10
18秒前
小林太郎发布了新的文献求助50
19秒前
20秒前
刺桐花下完成签到 ,获得积分10
21秒前
CipherSage应助mumufan采纳,获得10
21秒前
22秒前
22秒前
25秒前
liangzhy发布了新的文献求助10
26秒前
26秒前
sun发布了新的文献求助10
27秒前
落忆完成签到 ,获得积分10
28秒前
28秒前
oraen1发布了新的文献求助10
28秒前
29秒前
29秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Les Mantodea de Guyane Insecta, Polyneoptera 2500
Computational Atomic Physics for Kilonova Ejecta and Astrophysical Plasmas 500
Technologies supporting mass customization of apparel: A pilot project 450
Mixing the elements of mass customisation 360
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
the MD Anderson Surgical Oncology Manual, Seventh Edition 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3781828
求助须知:如何正确求助?哪些是违规求助? 3327403
关于积分的说明 10230923
捐赠科研通 3042284
什么是DOI,文献DOI怎么找? 1669963
邀请新用户注册赠送积分活动 799434
科研通“疑难数据库(出版商)”最低求助积分说明 758804