Foot-and-mouth disease virus infection of dendritic cells triggers phosphorylation of ERK1/2 inducing class I presentation and apoptosis

被引:9
|
作者
Langellotti, Cecilia [1 ,3 ]
Cesar, Gonzalo [2 ]
Soria, Ivana [1 ,3 ]
Quattrocchi, Valeria [1 ]
Jancic, Carolina [2 ,3 ]
Zamorano, Patricia [1 ,3 ]
Vermeulen, Monica [2 ,3 ]
机构
[1] Inst Nacl Tecnol Agr INTA Castelar, Ctr Invest Ciencias Vet, Inst Virol, Buenos Aires, DF, Argentina
[2] Acad Nacl Med Buenos Aires, CONICET, Inst Med Expt IMEX, Lab Inmunol, RA-1425 Buenos Aires, DF, Argentina
[3] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
关键词
Foot-and-mouth disease virus; Dendritic cells; Inactive viral particles; Caspase-9; ERK1/2; MAPK; Class I-restricted presentation; Cytotoxicity; ACTIVATED PROTEIN-KINASE; MHC CLASS-I; IMMUNE-RESPONSE; VACCINE; INTERFERON; INNATE; REPLICATION; EXPRESSION; COINCIDES; AUTOPHAGY;
D O I
10.1016/j.vaccine.2015.07.038
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals. This pathology is caused by foot-and-mouth disease virus (FMDV). Overtime, the development of vaccines to prevent the spread of this illness became essential. Vaccines currently used contain the inactivated form of the virus. However, vaccination generates an immune response different to that induced by the infection. We investigated whether these differences are related to intracellular mechanisms on dendritic cells (DCs). As a result, we demonstrated that the internalization of infective virus triggered the phosphorylation of ERK1/2, which was involved in the activation of caspase-9, the intrinsic pathway of apoptosis and the delivery of viral peptides on MHC class I molecules. While, inactivated virus (iFMDV) did not affect this pathway or any function mediated by its activation. As described, infectious virus in DCs was also associated to autophagy LC3 protein and was associated to lysosomal protein Lamp-2; contrary to observe for the iFMDV. Strikingly, the processing of viral antigens to accommodate in class I molecules does not appear to involve the proteasome. Finally, this increased presentation promotes a specific cytotoxic response against infectious virus. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4945 / 4953
页数:9
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