Opiate abuse, innate immunity, and bacterial infectious diseases

Jinghua Wang, Roderick A. Barke, Jing Ma, Richard Charboneau, Sabita Roy

Research output: Contribution to journalReview articlepeer-review

59 Scopus citations

Abstract

The first line of defense against invading bacteria is provided by the innate immune system. Morphine and other opiates can immediately disrupt the body's first line of defense against harmful external bacteria. Opiate, for example morphine, abuse degrades physical and physiologic barriers, and modulates phagocytic cells (macrophages, neutrophils) and, nonspecific cytotoxic T cells (γδ T), natural killer cells, and dendritic cells, that are functionally important for carrying out a rapid immune reaction to invading pathogens. In vitro studies with innate immune cells from experimental animals and humans and in vivo studies with animal models have shown that opiate abuse impairs innate immunity and is responsible for increased susceptibility to bacterial infection. However, to better understand the complex interactions between opiates, innate immunity, and bacterial infection and develop novel approaches to treat and even prevent bacterial infection in the opiate-abuse population, there is an urgent need to fill the numerous gaps in our understanding of the cellular and molecular mechanisms by which opiate abuse increases susceptibility to bacterial infection.

Original languageEnglish (US)
Pages (from-to)299-309
Number of pages11
JournalArchivum Immunologiae et Therapiae Experimentalis
Volume56
Issue number5
DOIs
StatePublished - Oct 2008

Bibliographical note

Funding Information:
Acknowledgment: This work was supported by grants R01 DA12104, K02 DA015349, P50 DA11806 (to S. Roy), and R03 DA023353 (to J. Wang) from the National Institutes of Health, and funds (to R. A. Barke) from the Minneapolis Veterans Affairs Medical Center.

Keywords

  • Bacterial infection
  • Cytokines
  • Dentritic cells
  • Innate immunity
  • Macrophages
  • Morphine
  • NK cells
  • Neutrophils
  • Opiate
  • γδ T lymphocytes

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