Cotter Catherine A, Ignacio Maxinne A, Americo Jeffrey L, Earl Patricia L, Mucker Eric M, Frey Tiffany R, Carfi Andrea, Hooper Jay W, Freyn Alec W, Moss Bernard
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
NPJ Vaccines. 2024 Dec 24;9(1):256. doi: 10.1038/s41541-024-01052-2.
We previously reported that mice immunized twice with a lipid nanoparticle vaccine comprising four monkeypox viral mRNAs raised neutralizing antibodies and antigen-specific T cells and were protected against a lethal intranasal challenge with vaccinia virus (VACV). Here we demonstrated that the mRNA vaccine also protects mice against intranasal and intraperitoneal infections with monkeypox virus and bioluminescence imaging showed that vaccination greatly reduces or prevents VACV replication and spread from intranasal, rectal, and dermal inoculation sites. A single vaccination provided considerable protection that was enhanced by boosting for at least 4 months. Protection was related to the amount of mRNA inoculated, which correlated with neutralizing antibody levels. Furthermore, immunocompetent and immunodeficient mice lacking mature B and T cells that received serum from mRNA-immunized macaques before or after VACV challenge were protected. These findings provide insights into the mechanism and extent of mRNA vaccine-induced protection of orthopoxviruses and support clinical testing.
我们之前报道过,用包含四种猴痘病毒信使核糖核酸(mRNA)的脂质纳米颗粒疫苗对小鼠进行两次免疫后,小鼠产生了中和抗体和抗原特异性T细胞,并对痘苗病毒(VACV)的致死性鼻内攻击具有保护作用。在此,我们证明该mRNA疫苗还能保护小鼠免受猴痘病毒的鼻内和腹腔感染,生物发光成像显示,接种疫苗可大大减少或阻止VACV从鼻内、直肠和皮肤接种部位复制和传播。单次接种提供了相当程度的保护,通过加强免疫至少4个月可增强这种保护作用。保护作用与接种的mRNA量有关,而mRNA量与中和抗体水平相关。此外,在VACV攻击之前或之后接受来自mRNA免疫食蟹猴血清的缺乏成熟B细胞和T细胞的免疫活性和免疫缺陷小鼠也受到了保护。这些发现为mRNA疫苗诱导的正痘病毒保护机制和程度提供了见解,并支持临床测试。