The risks of targeting co-inhibitory pathways to modulate pathogen-directed T cell responses

Trends Immunol. 2013 May;34(5):193-9. doi: 10.1016/j.it.2012.12.002. Epub 2013 Jan 16.

Abstract

The identification of T cell co-inhibition as a central mechanism in the regulation of adaptive immunity during infectious diseases provides new opportunities for immunotherapeutic interventions. However, the fact that T cell activity is frequently downregulated during pathogen-directed responses suggests a pivotal physiological role of co-inhibitory pathways during infectious disease. Reports of exacerbated immunopathology in conditions of impaired co-inhibition foster the view that downregulation of T cell activity is an essential negative feedback mechanism that protects from excessive pathogen-directed immunity. Thus, targeting co-inhibitory pathways can bear detrimental potential through the deregulation of physiological processes. Here, we summarize recent preclinical and clinical interventions that report immune-related adverse events after targeting co-inhibitory pathways.

Publication types

  • Review

MeSH terms

  • Animals
  • CTLA-4 Antigen / antagonists & inhibitors
  • CTLA-4 Antigen / immunology
  • Clinical Trials as Topic
  • Drug Evaluation, Preclinical
  • Humans
  • Immunity, Cellular / drug effects
  • Immunosuppressive Agents / adverse effects*
  • Immunosuppressive Agents / pharmacology
  • Immunosuppressive Agents / therapeutic use
  • Immunotherapy / adverse effects*
  • Immunotherapy / methods
  • Infections / complications*
  • Infections / immunology
  • Infections / therapy
  • Molecular Targeted Therapy / adverse effects*
  • Molecular Targeted Therapy / methods
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor / immunology
  • Receptor Cross-Talk / drug effects
  • Superinfection / etiology*
  • Superinfection / immunology
  • Superinfection / prevention & control
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / immunology

Substances

  • CTLA-4 Antigen
  • Immunosuppressive Agents
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor