封锁
接种疫苗
佐剂
CD8型
免疫学
T细胞
抗原
免疫疗法
免疫系统
医学
细胞毒性T细胞
病毒学
生物
受体
体外
内科学
生物化学
作者
Tomohiro Okagawa,Satoru Konnai,Hayato Nakamura,Otgontuya Ganbaatar,Yamato Sajiki,Kei Watari,Haruka Noda,Mitsuru Honma,Yukinari Kato,Yasuhiko Suzuki,Naoya Maekawa,Motoo Shiro,Kazuhiko Ohashi
出处
期刊:Vaccines
[MDPI AG]
日期:2023-03-01
卷期号:11 (3): 559-559
标识
DOI:10.3390/vaccines11030559
摘要
Interactions between programmed death 1 (PD-1) and PD-ligand 1 (PD-L1) cause functional exhaustion of T cells by inducing inhibitory signals, thereby attenuating effector functions of T cells. We have developed an anti-bovine PD-L1 blocking antibody (Ab) and have demonstrated that blockade of the interaction between PD-1 and PD-L1 reactivates T-cell responses in cattle. In the present study, we examined the potential utility of PD-1/PD-L1-targeted immunotherapy in enhancing T-cell responses to vaccination. Calves were inoculated with a hexavalent live-attenuated viral vaccine against bovine respiratory infections in combination with treatment with an anti-PD-L1 Ab. The expression kinetics of PD-1 in T cells and T-cell responses to viral antigens were measured before and after vaccination to evaluate the adjuvant effect of anti-PD-L1 Ab. PD-1 expression was upregulated in vaccinated calves after the administration of a booster vaccination. The activation status of CD4+, CD8+, and γδTCR+ T cells was enhanced by the combination of vaccination and PD-L1 blockade. In addition, IFN-γ responses to viral antigens were increased following combinatorial vaccination with PD-L1 blockade. In conclusion, the blockade of the PD-1/PD-L1 interaction enhances T-cell responses induced by vaccination in cattle, indicating the potential utility of anti-PD-L1 Ab in improving the efficacy of current vaccination programs.
科研通智能强力驱动
Strongly Powered by AbleSci AI