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Publication : IL-10 participates in the expansion and functional activation of CD8<sup>+</sup> T cells during acute infection with Trypanosoma cruzi.

First Author  Pino-Martínez AM Year  2019
Journal  J Leukoc Biol Volume  105
Issue  1 Pages  163-175
PubMed ID  30371945 Mgi Jnum  J:269232
Mgi Id  MGI:6272146 Doi  10.1002/JLB.3A0318-111RR
Citation  Pino-Martinez AM, et al. (2019) IL-10 participates in the expansion and functional activation of CD8(+) T cells during acute infection with Trypanosoma cruzi. J Leukoc Biol 105(1):163-175
abstractText  IL-10 is a pleiotropic cytokine with immunoregulatory functions affecting various cell types. In a model of experimental infection with the protozoan Trypanosoma cruzi (T. cruzi), we found increased morbidity and lower parasite control in IL-10 deficient mice (IL-10 KO) compared to wild-type (WT) mice. Despite enhanced Mvarphi function and dendritic cell activation, IL-10 KO mice were more susceptible to infection. The kinetics of T cells in spleen and peripheral blood revealed that infected IL-10 KO mice failed to increase the number of spleen and circulating total CD8(+) T cells, a phenomenon observed from the second week of infection in WT mice. Total CD8(+) T cells from IL-10 KO mice exhibited diminished proliferation, cytotoxic potential and IFN-gamma production than their WT counterparts and T. cruzi-specific CD8(+) T cells displayed reduced in vivo cytotoxicity. The absence of IL-10 selectively affected expansion, survival, and increased PD-1 expression of CD8(+) T cells without altering these same parameters on CD4(+) T cells. Increased inhibitory receptors expression and down-modulation of T-bet by CD8(+) T cells from IL-10 KO infected mice were compatible with a T cell exhaustion phenotype. Collectively, these findings reveal that during acute infection, IL-10 plays a previously unrecognized stimulatory role on CD8(+) T cells, the most relevant lymphocyte population for the control of intracellular T. cruzi stages. A clear knowledge of the underlying mechanisms that drive effector functions of cytotoxic T cells is critical to understand pathogen persistence and rational design of prophylactic strategies against T. cruzi.
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