dc.creator | Pontillo, Alessandra | |
dc.creator | Santillo, Bruna T | |
dc.creator | Duarte, Alberto J | |
dc.creator | Oshiro, Telma M | |
dc.date.accessioned | 2015-01-09T15:53:08Z | |
dc.date.accessioned | 2018-07-04T16:57:00Z | |
dc.date.available | 2015-01-09T15:53:08Z | |
dc.date.available | 2018-07-04T16:57:00Z | |
dc.date.created | 2015-01-09T15:53:08Z | |
dc.date.issued | 2013-12-27 | |
dc.identifier | AIDS Research and Therapy. 2013 Dec 27;10(1):35 | |
dc.identifier | http://dx.doi.org/10.1186/1742-6405-10-35 | |
dc.identifier | http://www.producao.usp.br/handle/BDPI/46921 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1642584 | |
dc.description.abstract | Abstract
Background
NLRP3-inflammasome activation was evaluated in monocyte-derived dendritic cells (DC) obtained through IL-4 (IL4-DC) or IFN-α (IFN-DC) protocols and pulsed with chemically inactivated HIV-1. Inflammasome’ genes expression and IL-1β secretion were compared in DC isolated from 15 healthy subjects (HC) and 10 HIV-1 infected individuals (HIV+).
Findings
Whether HIV was able to increased NLRP3-inflammasome genes expression and IL-1β secretion in IL4-DC from HC, the induction of inflammasome appeared significantly reduced in IFN-DC from HC, suggesting a different responsive state of IFN-DC compared to IL4-DC. No inflammasome activation was observed in IL4-DC as well as in IFN-DC derived from HIV + subjects, confirming previous findings on “unresponsive” state of DC derived from HIV + possibly due to chronic inflammatory state of these individuals.
Conclusions
Our results showed that IFN-α differently modulates inflammasome expression during monocytes-DC in vitro differentiation. These findings could be of interest considering the on-going research about DC manipulation and therapeutic strategies for HIV + involving DC-based immune-vaccines. | |
dc.language | en | |
dc.rights | Pontillo et al.; licensee BioMed Central Ltd. | |
dc.title | Differential inflammasome expression and IL-1β secretion in monocyte-derived dendritic cells differentiated with IL-4 or IFN-α | |