In vivo depletion of CD11c+ cells delays the CD4+ T cell response to Mycobacterium tuberculosis and exacerbates the outcome of infection

T Tian, J Woodworth, M Sköld… - The Journal of …, 2005 - journals.aai.org
T Tian, J Woodworth, M Sköld, SM Behar
The Journal of Immunology, 2005journals.aai.org
Although dendritic cells (DC) are potent APC that prime T cells against many pathogens,
there is no direct evidence that DC are required for immunity to Mycobacterium tuberculosis
(Mtb) infection. The requirement for DC to prime the CD4+ T cell response following Mtb
infection was investigated using pCD11c-diptheria toxin receptor/GFP transgenic mice, in
which DC can be transiently ablated in vivo. We show a critical role for DC in initiation of the
CD4+ T cell response to the mycobacterial Ag early secretory Ag of tuberculosis 6. The …
Abstract
Although dendritic cells (DC) are potent APC that prime T cells against many pathogens, there is no direct evidence that DC are required for immunity to Mycobacterium tuberculosis (Mtb) infection. The requirement for DC to prime the CD4+ T cell response following Mtb infection was investigated using pCD11c-diptheria toxin receptor/GFP transgenic mice, in which DC can be transiently ablated in vivo. We show a critical role for DC in initiation of the CD4+ T cell response to the mycobacterial Ag early secretory Ag of tuberculosis 6. The delay in initiating the Ag-specific T cell response led to impaired control of Mtb replication. Interestingly, DC were not required for the secondary CD4+ T cell response following Mtb infection in peptide-vaccinated mice. Thus, this study shows that DC are essential for the initiation of the adaptive T cell response to the human pathogen Mtb.
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