CD103+ pulmonary dendritic cells preferentially acquire and present apoptotic cell–associated antigen

Journal of Experimental Medicine - Tập 208 Số 9 - Trang 1789-1797 - 2011
A. Nicole Desch1,2,3, Gwendalyn J. Randolph4,5,6, Kenneth M. Murphy7, Emmanuel L. Gautier4,5,6, Ross M. Kedl1,2,3, Mireille H. Lahoud8,9, Irina Caminschi9, Ken Shortman8,9, Peter M. Henson1,10,2,3, Claudia Jakubzick1,10,2,3
1Department of Medicine 1 , 2 , and 3
2Department of Pediatrics, Department of Medicine, and Integrated Department of Immunology, National Jewish Health, University of Colorado Denver, Denver, CO 80206
3Integrated Department of Immunology, National Jewish Health, University of Colorado Denver, Denver, CO 80206 1 , 2 , and 3
4Department of Development Regenerative Biology 4 and 5
5Department of Development Regenerative Biology and Immunology Institute, Mount Sinai School of Medicine, New York, NY 10029
6Immunology Institute, Mount Sinai School of Medicine, New York, NY 10029 4 and 5
7Department of Pathology and Immunology, Washington University in St. Louis School of Medicine, St. Louis, MO 63130 6
8Department of Medical Biology, The University of Melbourne, Melbourne, Victoria 3010, Australia 8
9The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia 7
10Department of Pediatrics 1 , 2 , and 3

Tóm tắt

Cells undergoing programmed cell death (apoptosis) are removed in situ by macrophages and dendritic cells (DCs) through a specialized form of phagocytosis (efferocytosis). In the lung, there are two primary DC subsets with the potential to migrate to the local lymph nodes (LNs) and initiate adaptive immune responses. In this study, we show that only CD103+ DCs were able to acquire and transport apoptotic cells to the draining LNs and cross present apoptotic cell–associated antigen to CD8 T cells. In contrast, both the CD11bhi and the CD103+ DCs were able to ingest and traffic latex beads or soluble antigen. CD103+ DCs selectively exhibited high expression of TLR3, and ligation of this receptor led to enhanced in vivo cytotoxic T cell responses to apoptotic cell–associated antigen. The selective role for CD103+ DCs was confirmed in Batf3−/− mice, which lack this DC subtype. Our findings suggest that CD103+ DCs are the DC subset in the lung that captures and presents apoptotic cell–associated antigen under homeostatic and inflammatory conditions and raise the possibility for more focused immunological targeting to CD8 T cell responses.

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