Macrophages of the splenic marginal zone are essential for trapping of blood-borne particulate antigen but dispensable for induction of specific T cell responses

J Immunol. 2003 Aug 1;171(3):1148-55. doi: 10.4049/jimmunol.171.3.1148.

Abstract

Rapid removal of pathogens from the circulation by secondary lymphoid organs is prerequisite for successful control of infection. Blood-borne Ags are trapped mainly in the splenic marginal zone. To identify the cell populations responsible for Ag trapping in the marginal zone, mice were selectively depleted of marginal zone macrophages and marginal metallophilic macrophages. In the absence of these cells, trapping of microspheres and Listeria monocytogenes organisms was lost, and early control of infection was impaired. Depletion of marginal zone macrophages and marginal metallophilic macrophages, however, did not limit Ag presentation because Listeria-specific protective T cell immunity was induced. Therefore, marginal zone macrophages and marginal metallophilic macrophages are crucial for trapping of particulate Ag but dispensable for Ag presentation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigen-Presenting Cells / immunology
  • Antigen-Presenting Cells / metabolism
  • Antigen-Presenting Cells / microbiology
  • Antigens, Bacterial / blood*
  • Antimetabolites / administration & dosage
  • Clodronic Acid / administration & dosage
  • Epitopes, T-Lymphocyte / blood*
  • Immunity, Innate / immunology
  • Injections, Intravenous
  • Liposomes
  • Listeria monocytogenes / growth & development
  • Listeria monocytogenes / immunology
  • Listeriosis / immunology
  • Listeriosis / microbiology
  • Lymphocyte Activation*
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Organ Specificity / immunology
  • Spleen / blood supply*
  • Spleen / cytology
  • Spleen / immunology*
  • Spleen / microbiology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism*
  • T-Lymphocyte Subsets / microbiology

Substances

  • Antigens, Bacterial
  • Antimetabolites
  • Epitopes, T-Lymphocyte
  • Liposomes
  • Clodronic Acid