Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Department of Parasitology, Inje University College of Medicine, Busan, 47392, Republic of Korea.
Nanomedicine (Lond). 2024;19(29):2437-2446. doi: 10.1080/17435889.2024.2403333. Epub 2024 Sep 25.
To evaluate the protective efficacy induced by heterologous immunization with recombinant baculoviruses or virus-like particles targeting the CST1 and ROP18 antigens of .: Recombinant baculovirus and virus-like particle vaccines expressing CST1 or ROP18 antigens were developed to evaluate protective immunity in mice upon challenge infection with 450 (ME49). Immunization with CST1 or ROP18 vaccines induced similar levels of -specific IgG and IgA responses. Compared with ROP 18, CST1 vaccine showed better antibody-secreting cell response, germinal center B cell activation, and significantly reduced brain cyst burden and body weight loss. Our findings suggest that CST1 heterologous immunization elicited better protection than ROP18, providing important insight into improving the toxoplasmosis vaccine design strategy.
为了评估针对 CST1 和 ROP18 抗原的重组杆状病毒或病毒样颗粒异源免疫诱导的保护效力:开发了表达 CST1 或 ROP18 抗原的重组杆状病毒和病毒样颗粒疫苗,以评估在 450 (ME49)挑战感染后小鼠的保护性免疫。CST1 或 ROP18 疫苗免疫诱导了相似水平的 -特异性 IgG 和 IgA 反应。与 ROP18 相比,CST1 疫苗显示出更好的抗体分泌细胞反应、生发中心 B 细胞激活,并且显著降低脑囊泡负担和体重减轻。我们的研究结果表明,CST1 异源免疫诱导的保护作用优于 ROP18,为改善弓形虫病疫苗设计策略提供了重要的见解。