dc.creator | Aggio, Juliana Bernardi | |
dc.creator | Krmeska, Veronika | |
dc.creator | Ferguson, Brian J. | |
dc.creator | Wowk, Pryscilla Fanini | |
dc.creator | Rothfuchs, Antonio Gigliotti | |
dc.date | 2021-03-12T18:49:54Z | |
dc.date | 2021-03-12T18:49:54Z | |
dc.date | 2021 | |
dc.date.accessioned | 2023-09-26T21:37:31Z | |
dc.date.available | 2023-09-26T21:37:31Z | |
dc.identifier | AGGIO, Juliana Bernardi et al. Vaccinia virus infection inhibits skin dendritic cell migration to the draining lymph node. The Journal of Immunology, p. 776-784, 2021. | |
dc.identifier | 1550-6606 | |
dc.identifier | https://www.arca.fiocruz.br/handle/icict/46354 | |
dc.identifier | https://doi.org/10.4049/jimmunol.2000928 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8873039 | |
dc.description | There is a paucity of information on dendritic cell (DC) responses to vaccinia virus (VACV), including the traffic of DCs to the draining lymph node (dLN). In this study, using a mouse model of infection, we studied skin DC migration in response to VACV and compared it with the tuberculosis vaccine Mycobacterium bovis bacille Calmette–Gue´rin (BCG), another live attenuated vaccine administered via the skin. In stark contrast to BCG, skin DCs did not relocate to the dLN in response to VACV. Infection with UV-inactivated VACV or modified VACVAnkara promoted DC movement to the dLN, indicating that interference with skin DC migration requires replication-competent VACV. This suppressive effect of VACV was capable of mitigating responses to a secondary challenge with BCG in the skin, ablating DC migration, reducing BCG transport, and delaying CD4+ T cell priming in the dLN. Expression of inflammatory mediators associated with BCG-triggered DC migration were absent from virus-injected skin, suggesting that other pathways invoke DC movement in response to replication-deficient VACV. Despite adamant suppression of DC migration, VACV was still detected early in the dLN and primed Ag-specific CD4+ T cells. In summary, VACV blocks skin DC mobilization from the site of infection while retaining the ability to access the dLN to prime CD4+ T cells. | |
dc.format | application/pdf | |
dc.language | por | |
dc.publisher | The American Association of Immunologists | |
dc.rights | open access | |
dc.subject | Bacillus Calmette-Guérin | |
dc.subject | BCG | |
dc.subject | Vaccinia virus | |
dc.subject | Dendritic Cells | |
dc.subject | Lymph Nodes | |
dc.subject | CD4-Positive T-Lymphocytes | |
dc.subject | Virus Vaccinia | |
dc.subject | Células Dendríticas | |
dc.subject | Ganglios Linfáticos | |
dc.subject | Linfocitos T CD4-Positivos | |
dc.subject | Virus de la vaccine | |
dc.subject | Cellules dendritiques | |
dc.subject | Noeuds lymphatiques | |
dc.subject | Lymphocytes T CD4+ | |
dc.subject | Vírus Vaccinia | |
dc.subject | Células Dendríticas | |
dc.subject | Mycobacterium bovis | |
dc.subject | Linfonodos | |
dc.subject | Linfócitos T CD4-Positivos | |
dc.title | Vaccinia virus infection inhibits skin dendritic cell migration to the draining lymph node | |
dc.type | Article | |