Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Blocking of Opioid Receptors in Experimental Formaline-Inactivated Respiratory Syncytial Virus (Fi-Rsv) Immunopathogenesis: From Beneficial to Harmful Impacts Publisher Pubmed



Salimi V1 ; Mirzaei H1 ; Ramezani A1 ; Tahamtan A1, 2 ; Jamali A3 ; Shahabi S4 ; Golaram M5 ; Minaei B6 ; Gharagozlou MJ7 ; Mahmoodi M8 ; Bont L9 ; Shokri F5 ; Mokhtariazad T1
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Microbiology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran
  3. 3. Influenza and Other Respiratory Viruses Department, Pasteur Institute of Iran, Tehran, Iran
  4. 4. Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran
  5. 5. Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Anatomy, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  8. 8. Epidemiology and Biostatistics Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Department of Paediatrics, Wilhelmina Children’s Hospital, University Medical Centre Utrecht, Utrecht, Netherlands

Source: Medical Microbiology and Immunology Published:2018


Abstract

Opioid system plays a significant role in pathophysiological processes, such as immune response and impacts on disease severity. Here, we investigated the effect of opioid system on the immunopathogenesis of respiratory syncytial virus (RSV) vaccine (FI-RSV)-mediated illness in a widely used mouse model. Female Balb/c mice were immunized at days 0 and 21 with FI-RSV (2 × 106 pfu, i.m.) and challenged with RSV-A2 (3 × 106 pfu, i.n.) at day 42. Nalmefene as a universal opioid receptors blocker administered at a dose of 1 mg/kg in combination with FI-RSV (FI-RSV + NL), and daily after live virus challenge (RSV + NL). Mice were sacrificed at day 5 after challenge and bronchoalveolar lavage (BAL) fluid and lungs were harvested to measure airway immune cells influx, T lymphocyte subtypes, cytokines/chemokines secretion, lung histopathology, and viral load. Administration of nalmefene in combination with FI-RSV (FI-RSV + NL-RSV) resulted in the reduction of the immune cells infiltration to the BAL fluid, the ratio of CD4/CD8 T lymphocyte, the level of IL-5, IL-10, MIP-1α, lung pathology, and restored weight loss after RSV infection. Blocking of opioid receptors during RSV infection in vaccinated mice (FI-RSV-RSV + NL) had no significant effects on RSV immunopathogenesis. Moreover, administration of nalmefene in combination with FI-RSV and blocking opioid receptors during RSV infection (FI-RSV + NL-RSV + NL) resulted in an increased influx of the immune cells to the BAL fluid, increases the level of IFN-γ, lung pathology, and weight loss in compared to control condition. Although nalmefene administration within FI-RSV vaccine decreases vaccine-enhanced infection during subsequent exposure to the virus, opioid receptor blocking during RSV infection aggravates the host inflammatory response to RSV infection. Thus, caution is required due to beneficial/harmful functions of opioid systems while targeting as potentially therapies. © 2017, Springer-Verlag GmbH Germany, part of Springer Nature.
Other Related Docs
13. The Molecular Epidemiology of Respiratory Viruses in Military Trainees in Iran, Medical Journal of the Islamic Republic of Iran (2019)