Induction of antiviral immunity requires Toll-like receptor signaling in both stromal and dendritic cell compartments

  1. Ayuko Sato and
  2. Akiko Iwasaki*
  1. Section of Immunobiology, Yale University School of Medicine, New Haven, CT 06520
  1. Edited by Ralph M. Steinman, The Rockefeller University, New York, NY, and approved October 7, 2004 (received for review August 25, 2004)

Abstract

Pattern recognition by Toll-like receptors (TLRs) is known to be important for the induction of dendritic cell (DC) maturation. DCs, in turn, are critically important in the initiation of T cell responses. However, most viruses do not infect DCs. This recognition system poses a biological problem in ensuring that most viral infections be detected by pattern recognition receptors. Furthermore, it is unknown what, if any, is the contribution of TLRs expressed by cells that are infected by a virus, versus TLRs expressed by DCs, in the initiation of antiviral adaptive immunity. Here we address these issues using a physiologically relevant model of mucosal infection with herpes simplex virus type 2. We demonstrate that innate immune recognition of viral infection occurs in two distinct stages, one at the level of the infected epithelial cells and the other at the level of the noninfected DCs. Importantly, both TLR-mediated recognition events are required for the induction of effector T cells. Our results demonstrate that virally infected tissues instruct DCs to initiate the appropriate class of effector T cell responses and reveal the critical importance of the stromal cells in detecting infectious agents through their own pattern recognition receptors.

Footnotes

  • * To whom correspondence should be addressed. E-mail: akiko.iwasaki{at}yale.edu.

  • Author contributions: A.S. performed research; A.S. and A.I. analyzed data; A.S. and A.I. wrote the paper; and A.I. designed research.

  • This paper was submitted directly (Track II) to the PNAS office.

  • Abbreviations: Ag, antigen; APC, Ag-presenting cell; BM, bone marrow; DC, dendritic cell; HSV, herpes simplex virus; ivag, intravaginal(ly); KO, knockout; PAMP, pathogen-associated molecular pattern; p.i., postinfection; PRR, pattern recognition receptor; Th, T helper; TLR, Toll-like receptor.

  • See Commentary on page 16083.

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