Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)-Peptide Tetramers

• Published in: Viruses 2021-11, Vol.13 (11), p.2264
• Main Authors: Sun, Wenqiang, Zhang, He, Fan, Wenhui, He, Lihong, Chen, Teng, Zhou, Xintao, Qi, Yu, Sun, Lei, Hu, Rongliang, Luo, Tingrong, Liu, Wenjun, Li, Jing
• Format: Article
• Language: English
• Subjects: African swine fever; African Swine Fever - immunology; African swine fever virus; African Swine Fever Virus - immunology; Animals; Antibodies; Antigens; Antigens, Viral - immunology; Asfarviridae; Capsid Proteins - immunology; Cell-mediated immunity; Cloning; Disease; Epitopes; Epitopes, T-Lymphocyte - chemistry; Epitopes, T-Lymphocyte - immunology; Ethics; Farms; Hemorrhage; Hemorrhagic fever; Histocompatibility Antigens Class I - chemistry; Histocompatibility Antigens Class I - immunology; Hogs; Immune response (humoral); Immunity, Cellular - immunology; Immunity, Humoral - immunology; Infections; Lymphocytes; Lymphocytes T; Molecular Docking Simulation; p72; p72 Protein; Peptides; protective antigen; Proteins; Swine; T cell immune response; T epitopes; T-Lymphocytes - immunology; Vaccines; Veterinary medicine; Virulence; Viruses
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v13112264

African swine fever virus (ASFV) causes acute hemorrhagic fever in domestic pigs and wild boars, resulting in incalculable economic losses to the pig industry. As the mechanism of viral infection is not clear, protective antigens have not been discovered or identified. In this study, we determined that the p30, pp62, p72, and CD2v proteins were all involved in the T cell immune response of live pigs infected with ASFV, among which p72 and pp62 proteins were the strongest. Panoramic scanning was performed on T cell epitopes of the p72 protein, and three high-frequency positive epitopes were selected to construct a swine leukocyte antigen (SLA)-tetramer, and ASFV-specific T cells were detected. Subsequently, the specific T cell and humoral immune responses of ASFV-infected pigs and surviving pigs were compared. The results demonstrate that the specific T cellular immunity responses gradually increased during the infection and were higher than that in the surviving pigs in the late stages of infection. The same trend was observed in specific humoral immune responses, which were highest in surviving pigs. In general, our study provides key information for the exploration of ASFV-specific immune responses and the development of an ASFV vaccine.