A multimodality therapeutic application on Toxoplasma gondii encephalitis utilizing Spiramycin and ‘de novo’ Ferula asafetida in immunodeficient mice

Theodor Bilharz Research Institute

Bibliographic Information

Authors: Almurshidi B.H.; Fahmy Z.; El-Shennawy A.; Selim E.A.H.; Hammam O.A.; Okasha H.; Al-Hajj W.; Mahmoud S.A.; Abuelenain G.L.

Journal: Parasite Immunology

Publisher: John Wiley and Sons Inc

Publication Date: 9 October 2023

Volume / Issue: Volume 45 / Issue 12

Article No.: e13014

ISSN: 1419838

DOI: 10.1111/pim.13014

Scopus: View on Scopus

PubMed: 37807942

Document Type: Article


Authors and Affiliations

Almurshidi B.H., Biology Department, United Arab Emirates University, Al Ain, United Arab Emirates; Fahmy Z., Immunology and Therapeutic Evaluation Department, Theodor Bilharz Research Institute, Giza, Egypt; El-Shennawy A., Immunology and Therapeutic Evaluation Department, Theodor Bilharz Research Institute, Giza, Egypt; Selim E.A.H., Immunology and Therapeutic Evaluation Department, Theodor Bilharz Research Institute, Giza, Egypt; Hammam O.A., Pathology Department, Theodor Bilharz Research Institute, Giza, Egypt; Okasha H., Biochemistry and Molecular Biology Department, Theodor Bilharz Research Institute, Giza, Egypt; Al-Hajj W., Fatima College of Health Sciences, IAT, Abu Dhabi, United Arab Emirates; Mahmoud S.A., Fatima College of Health Sciences, IAT, Abu Dhabi, United Arab Emirates, Cancer Science Institute, National University of Singapore, Singapore, Singapore; Abuelenain G.L., Immunology and Therapeutic Evaluation Department, Theodor Bilharz Research Institute, Giza, Egypt


Abstract

This study investigated a ‘de Novo’ medicinal herb, Ferula asafetida (FA), against toxoplasma encephalitis either alone or combined with spiramycin (SP). Female Swiss-Webster mice (n = 72) were divided into three batches. Batch-I received no DMS to serve as an immunocompetent control, batch-II was immune-suppressed with the DMS (0.25 mg/g/day) for 14 days pre-infection, whilst batch-III was immune-suppressed with the DMS on the same day of infection. All experimental mice were inoculated with Toxoplasma gondii ME49 cysts (n = 75). Each batch was split into four subgroups: Mono-SP, mono-FA, combined drug (SP + FA), or neither. Therapies were administered on day zero of infection in batches (I and II) and 35 days post-infection in batch (III). Treatments lasted for 14 days, and mice were sacrificed 60 days post-infection. Histopathological changes, cysts load, and CD4 and CD8 T-cells were counted in brain tissues. The cyst-load count in mice receiving SP + FA was significantly (p <.0001) the least compared to the mono treatments in all protocols. Interestingly, the combined therapy demolished the T-cell subsets to zero in immunocompetent and immunocompromised infected mice. In conclusion, F. asafetida might be a powerfully natural, safe vehicle of SP in the digestive system and/or across the brain–blood barrier to control toxoplasmosis even through immunodeficient conditions. © 2023 John Wiley & Sons Ltd.


Keywords

drug discovery; Ferula ass-foetida; spiramycin, medicinal herbs; toxoplasmosis encephalitis; antiprotozoal agent; Ferula asafetida extract; plant extract; spiramycin; unclassified drug; animal cell; animal experiment; animal model; animal tissue; Article; brain tissue; CD4+ T lymphocyte; CD8+ T lymphocyte; cerebral toxoplasmosis; controlled study; cyst (resting stage); female; Ferula; Ferula asafetida; gene dosage; histopathology; immunohistochemistry; mouse; nonhuman; parasite load; recommended drug dose; T lymphocyte subpopulation; Toxoplasma gondii


Citation Information

Scopus Citations: 1


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