Protection and Immune Responses Elicited by rSAG۱-PLGA Nanoparticles in C۵۷BL/۶ Against Toxoplasma gondii
Publish Year: 1399
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_JMMI-9-1_007
تاریخ نمایه سازی: 29 بهمن 1402
Abstract:
Introduction: This study aimed to evaluate rSAG۱-PLGA efficacy as a particulate vaccine in conferring protection against Toxoplasma gondii infection in C۵۷BL/۶ mice. In light of our previous studies, we studied mice genotype role in eliciting immune responses by rSAG۱-PLGA nanoparticles in this study. Methods: Poly (DL-lactide-co-glycolide) (PLGA) nanoparticles loaded by rSAG۱ as a subunit vaccine were prepared, and C۵۷BL/۶ mice were subcutaneously immunized twice at a ۳-week interval by rSAG۱-PLGA, soluble rSAG۱, blank PLGA, and one group kept unvaccinated. The characteristics of PLGA nanoparticles, the amounts of produced IFN-γ, IL-۱۰, specific anti-ToxoplasmaIgGs, and the conferred protection against infection by T. gondii RH tachyzoite were assessed. Results: rSAG۱-PLGA nanoparticles shared a z-average of about ۴۵۰nm with negative Zeta potential. Compared with the negative control group, the mice vaccinated with rSAG۱-PLGA nanoparticles produced significantly higher amounts of IFN-γ, specific anti-T. gondii IgG antibodies and higher titer of IgG۲a, which resulted in longer survival times. Conclusion: The efficiency of rSAG۱-PLGA nanoparticles in inducing humoral and cellular responses and consequently partial protection against acute toxoplasmosis in C۵۷BL/۶ was confirmed.
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Authors
Mojgan Allahyari
Recombinant Protein Production Department, Production and Research Complex, Pasteur Institute of Iran, Karaj, Iran.
Samira amiri
Molecular Parasitology Laboratory, Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
Alireza Vatanara
Department of Pharmaceutics, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Majid Golkar
Molecular Parasitology Laboratory, Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran.
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