
Dendritic Cell Cross-Priming Is Essential for Immune Responses to Listeria monocytogenes
Author(s) -
Anna T. Reinicke,
Kyla Omilusik,
Genc Basha,
Wilfred A. Jefferies
Publication year - 2009
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0007210
Subject(s) - priming (agriculture) , cross presentation , listeria monocytogenes , immune system , biology , listeria , antigen , listeria infection , cytotoxic t cell , immunology , t cell , antigen presentation , cd8 , microbiology and biotechnology , in vitro , bacteria , biochemistry , botany , germination , genetics
Cross-presentation is now recognized as a major mechanism for initiating CD8 T cell responses to virus and tumor antigens in vivo . It provides an elegant mechanism that allows relatively few Dendritic cells (DCs) to initiate primary immune responses while avoiding the consumptive nature of pathogenic infection. CD8 T cells play a major role in anti-bacterial immune responses; however, the contribution of cross-presentation for priming CD8 T cell responses to bacteria, in vivo , is not well established. Listeria monocytogenes ( Listeria ) is the causative agent of Listeriosis, an opportunistic food-borne bacterial infection that poses a significant public health risk. Here, we employ a transgenic mouse model in which cross-presentation is uniquely inactivated, to investigate cross-priming during primary Listeria infection. We show that cross-priming deficient mice are severely compromised in their ability to generate antigen-specific T cells to stimulate MHC I-restricted CTL responses following Listeria infection. The defect in generation of Listeria -elicited CD8 T cell responses is also apparent in vitro . However, in this setting, the endogenous route of processing Listeria -derived antigens is predominant. This reveals a new experimental dichotomy whereby functional sampling of Listeria -derived antigens in vivo but not in vitro is dependent on cross-presentation of exogenously derived antigen. Thus, under normal physiological circumstances, cross-presentation is demonstrated to play an essential role in priming CD8 T cell responses to bacteria.