Published online 3 July 2006 doi:10.1084/jem.20052545
Rockefeller University Press, 0022-1007 $8.00
JEM, Volume 203, Number 7, 1805-1815
Interleukin 12p40 is required for dendritic cell migration and T cell priming after Mycobacterium tuberculosis infection
Shabaana A. Khader1,
Santiago Partida-Sanchez1,
Guy Bell1,
Dawn M. Jelley-Gibbs1,
Susan Swain1,
John E. Pearl1,
Nico Ghilardi2,
Frederic J. deSauvage2,
Frances E. Lund1, and
Andrea M. Cooper1
1 Trudeau Institute, Inc., Saranac Lake, NY 12983
2 Genentech Inc., South San Francisco, CA 94080
CORRESPONDENCE Andrea M. Cooper: acooper{at}trudeauinstitute.org
Migration of dendritic cells (DCs) to the draining lymph node (DLN) is required for the activation of naive T cells. We show here that migration of DCs from the lung to the DLN after Mycobacterium tuberculosis (Mtb) exposure is defective in mice lacking interleukin (IL)-12p40. This defect compromises the ability of IL-12p40deficient DCs to activate naive T cells in vivo; however, DCs that express IL-12p40 alone can activate naive T cells. Treatment of IL-12p40deficient DCs with IL-12p40 homodimer (IL-12(p40)2) restores Mtb-induced DC migration and the ability of IL-12p40deficient DCs to activate naive T cells. These data define a novel and fundamental role for IL-12p40 in the pathogen-induced activation of pulmonary DCs.
Abbreviations used: BMDC, bone marrowderived DC; DLN, draining LN; Mtb, Mycobacterium tuberculosis; Tg, transgenic.
S. Partida-Sanchez's present address is Columbus Children's Research Institute, Columbus, OH 43205.

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