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A Survey on the Adjuvant Role of Naloxone Alone or Combined With Alum in Vaccination Against Fasciolosis in Balb/C Mice Publisher Pubmed



Azizi H1 ; Mirzaeei H2 ; Bagheri A3 ; Bazi A4 ; Khamesipour A5 ; Yaghoobi H6 ; Mirzapour A7 ; Khatami M8 ; Elikaee S9
Authors
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Authors Affiliations
  1. 1. Department of Medical Parasitology, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran
  2. 2. Department of Medical Genetics, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran
  3. 3. Faculty of Veterinary Medicine, Sciences and Research Branch, Islamic Azad University, Tehran, Iran
  4. 4. Clinical Research Development Unit, Zabol University of Medical Sciences, Zabol, Iran
  5. 5. Skin and Leprosy Research Center, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran
  7. 7. Department of Medical Parasitology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  8. 8. School of Medicine, Bam University of Medical Sciences, Bam, Iran
  9. 9. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

Source: Acta Parasitologica Published:2019


Abstract

Background: Fasciolosis is a zoonotic parasitic disease imposing a heavy load of livestock losses worldwide. Purpose: We aimed to evaluate immune-stimulatory effects of naloxone (NLX), an opioid receptor antagonist, in combination with alum in mice vaccinated with excretory–secretory antigens (E/S) of Fasciola hepatica. Methods: 8-week-old female BALB/c mice were subcutaneously vaccinated using E/S antigens of F. hepatica. Experimental groups (14 mice per group) included: vaccine (E/S antigen), alum vaccine (E/S antigen plus alum), NLX vaccine (E/S antigen plus NLX), and alum–NLX vaccine (E/S antigen plus a mixture of alum–NLX). The control group was infused with PBS. Lymphocyte proliferation and the levels of IFN-γ, IL-4, IgG2a, IgG1, and total IgG were measured. Results: Mice vaccinated with NLX or alum–NLX adjuvants showed significantly higher rates of lymphocyte proliferation, IFN-γ, total IgG, and IgG2a levels. The mice that were injected with alum showed a significantly higher concentration of IL-4. Ratios of IFN-γ/Il-4 and IgG2a/IgG1 were significantly higher in the NLX and alum–NLX groups in comparison with the groups vaccinated either with alum or without any adjuvant. A significantly higher protection rate (62.5%) was seen in mice vaccinated with the alum–NLX adjuvant compared to the other groups. Conclusion: NLX can be effective in conferring cellular immunity and protection against F. hepatica. It is recommended to consider this agent as a potential adjuvant in vaccines against fasciolosis. © 2019, Witold Stefanski Institute of Parasitology, Polish Academy of Sciences.