Hydroxychloroquine: from malaria to autoimmunity

Clin Rev Allergy Immunol. 2012 Apr;42(2):145-53. doi: 10.1007/s12016-010-8243-x.

Abstract

Quinine was first recognized as a potent antimalarial agent hundreds of years ago. Since then, the beneficial effects of quinine and its more advanced synthetic forms, chloroquine and hydroxychloroquine, have been increasingly recognized in a myriad of other diseases in addition to malaria. In recent years, antimalarials were shown to have various immunomodulatory effects, and currently have an established role in the management of rheumatic diseases, such as systemic lupus erythematosus and rheumatoid arthritis, skin diseases, and in the treatment of chronic Q fever. Lately, additional metabolic, cardiovascular, antithrombotic, and antineoplastic effects of antimalarials were shown. In this review, we discuss the known various immunomodulatory mechanisms of antimalarials and the current evidence for their beneficial effects in various diseases and in potential novel applications.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage*
  • Anti-Inflammatory Agents / adverse effects
  • Antigen Presentation / drug effects
  • Antimalarials / administration & dosage*
  • Antimalarials / adverse effects
  • Autoimmune Diseases / drug therapy*
  • Autoimmune Diseases / immunology
  • Autoimmunity / drug effects
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology
  • Calcium Signaling / drug effects
  • Calcium Signaling / immunology
  • Cytokines / metabolism
  • Humans
  • Hydroxychloroquine / administration & dosage*
  • Hydroxychloroquine / adverse effects
  • Macrophages / drug effects
  • Macrophages / immunology
  • Malaria / drug therapy*
  • Malaria / immunology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Toll-Like Receptors / immunology

Substances

  • Anti-Inflammatory Agents
  • Antimalarials
  • Cytokines
  • Toll-Like Receptors
  • Hydroxychloroquine