Endogenous IL-1R1 Signaling Is Critical for Cognate CD4+ T Cell Help for Induction of In Vivo Type 1 and Type 2 Antipolysaccharide and Antiprotein Ig Isotype Responses to Intact Streptococcus pneumoniae, but Not to a Soluble Pneumococcal Conjugate Vaccine

Abstract

Interleukin-1 and IL-1 are proinflammatory cytokines that exert largely overlapping biological effects, both inducing cell signaling exclusively through IL-1R1 (1). Soluble IL-1R antagonist also binds to IL-1R1 but does not exert agonistic activity, serving instead to block IL-1 and IL- activity (2). IL-1RII also binds IL-1 but does not mediate signaling. IL-1 plays a key role in mediating innate host protection in response to pathogens, but is also a major inducer of tissue damage during infections and in pathologic conditions such as asthma and various autoimmune diseases (3, 4). IL-1 also exerts effects on cells involved in the adaptive immune response, acting directly as a costimulus for T cells (5), B cells (6), and dendritic cells (DCs)4 (7).

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 2006
Accession Number
ADA534627

Entities

People

  • Clifford M Snapper
  • Goutam Sen
  • Quanyi Chen

Organizations

  • Uniformed Services University of the Health Sciences

Tags

DTIC Thesaurus Topics

  • Adaptive Immunity
  • Bacteria
  • Blood
  • Cells
  • Cellular Structures
  • Gram-Positive Bacterial Infections
  • Humoral Immunity
  • Immunization
  • Infection
  • Lymphatic System
  • Lymphocytes
  • Macrophages
  • Mononuclear Phagocyte System
  • Proteins
  • T Lymphocytes
  • Tissues
  • Vaccines

Fields of Study

  • Medicine

Readers

  • Immunology
  • Neurological Diseases/Conditions/Disorders
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech