首页|猴痘病毒新型蛋白疫苗制备及其诱导抗体能力评估

猴痘病毒新型蛋白疫苗制备及其诱导抗体能力评估

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目的 构建有效的猴痘病毒(MPXV)和痘苗病毒(VACV)蛋白疫苗,并对其诱导抗体的活性进行初步评估.方法 采用融合蛋白表达技术构建MPXV-A29-Fc和VACV-A27-Fc蛋白疫苗,酶联免疫吸附试验(ELISA)和蛋白质印迹法(Western blot,WB)体外检测蛋白结合抗体的能力,BALB/c雌性小鼠体内评估不同剂量蛋白疫苗诱导抗体的效价.结果 MPXV-A29-Fc和VACV-A27-Fc蛋白均能与A29单克隆抗体结合,蛋白疫苗免疫小鼠后,不同剂量组中的小鼠血清均可交叉识别MPXV-A29和VACV-A27蛋白,三针免疫可诱导更强的交叉免疫应答,三针免疫后,不同的血清稀释度下,低剂量组的IgG抗体结合强度均与高剂量组相当,可达到高剂量组的免疫效果.结论 本研究初步构建有效的MPXV和VACV新型蛋白疫苗MPXV-A29-Fc和VACV-A27-Fc,在小鼠体内可诱导特异性抗体反应和交叉抗体反应,可为猴痘病毒的疫苗设计提供新的思路和方法.
Construction of a novel protein vaccine against monkeypox virus and evaluation of its immune response
Objective To construct monkeypoxvirus(MPXV)and vaccinia virus(VACV)protein vaccines and evaluate antibody activity induced by them.Methods MPXV-A29-Fc and VACV-A27-Fc protein vac-cines were constructed by fusion protein expression technology.The binding capacity of proteins was de-tected by ELISA and WB in vitro.Titer of antibody elicited by the protein was detected by immunizing fe-male BALB/c mice in vivo.Results Both MPXV-A29-Fc and VACV-A27-Fc proteins could bind to A29 mAb.MPXV-A29 and VACV-A27 proteins can be cross-recognized by the serum of mice immunized with MPXV-A29-Fc and VACV-A27-Fc proteins.3-dose vaccination could induce stronger cross-immune re-sponses.After 3 doses of MPXV-A29-Fc or VACV-A27-Fc in mice,the binding capacity of IgG antibody in the low-dose group was similar to that in the high-dose group at different serum dilutions,which could achieve the effective vaccination of the high-dose group.Conclusions In this study,novel vaccines MPXV-A29-Fc and VACV-A27-Fc,which can induce specific antibody response and cross-antibody response in mice,and they are successfully prepared.It provides a new idea and candidate for the design of MPXV vaccine.

monkeypox virus(MPXV)recombinant protein vaccinebinding activitycross reactivity

赵成燕、周兵、闫虎、李文婷、孙岳宏、鞠斌、张政、鲁晓擘

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新疆医科大学第一附属医院感染·肝病中心,乌鲁木齐 830054

深圳市第三人民医院肝病研究所,广东 深圳 518112

猴痘病毒(MPXV) 重组蛋白疫苗 结合活性 交叉反应性

国家自然科学基金国家自然科学基金

8206011582025022

2024

新疆医科大学学报
新疆医科大学

新疆医科大学学报

CSTPCD
影响因子:0.76
ISSN:1009-5551
年,卷(期):2024.47(5)