Improvement of the inactivated SARS-CoV-۲ vaccine potency through formulation in alum/naloxone adjuvant; Robust T cell and anti-RBD IgG responses

سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 196

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شناسه ملی سند علمی:

JR_IJBMS-25-5_002

تاریخ نمایه سازی: 21 خرداد 1401

چکیده مقاله:

Objective(s): SARS-CoV-۲, emerging as a major threat to public health, has to be controlled through vaccination. Naloxone (NLX), an opioid receptor antagonist, demonstrated its adjuvant activity for microbial vaccines. In this study, inactivated SARS-CoV-۲ was developed in the Alum/NLX adjuvant to increase the potency of the inactivated SARS-CoV-۲ vaccine. Materials and Methods: BALB/c mice were immunized on days ۰ and ۱۴ with inactivated SARS-CoV-۲-Alum, -Alum + NLX ۳ mg/kg, -Alum + NLX ۱۰ mg/kg, and -Freund adjuvant, as well as PBS. IFN-γ and IL-۴ cytokines and Granzyme-B release were assessed with ELISA. In addition, specific total IgG, IgG۱/IgG۲a isotypes, and ratio as well as anti-RBD IgG responses were assessed with an optimized ELISA. Results: SARS-CoV-۲-Alum-NLX۱۰ group showed a significant increase in the IFN-γ cytokine response versus SARS-CoV-۲-Alum, SARS-CoV-۲-Alum-NLX۳, and PBS groups. The SARS-CoV-۲-Alum-NLX۳ group exhibited a significant decrease in IL-۴ cytokine versus SARS-CoV-۲-Alum. The mice immunized with SARS-CoV-۲-Alum-NLX۱۰ showed a significant increase in CTL activity versus SARS-CoV-۲-Alum and PBS. In addition, mice immunized with SARS-CoV-۲-Alum-NLX۳, SARS-CoV-۲-Alum-NLX۱۰ and SARS-CoV-۲-Freund demonstrated an increase in IgG response, as compared with SARS-CoV-۲-Alum and PBS group. Furthermore, all formulations of SARS-CoV-۲ vaccines could induce both IgG۱ and IgG۲a isotypes. But, the IgG۲a/IgG۱ ratio in SARS-CoV-۲-Freund and SARS-CoV-۲-Alum-NLX۱۰ revealed an increase as compared with that of the SARS-CoV-۲-Alum group. Anti-RBD IgG response in the SARS-CoV-۲-Alum-NLX۱۰ group showed a significant increase as compared with the Alum-based vaccine. Conclusion: Formulation of inactivated SARS-CoV-۲ virus in NLX/alum adjuvant improved the potency of humoral and, especially, cellular responses.

کلیدواژه ها:

Alum Adjuvant ، Immune responses ، Inactivated SARS-CoV-۲ - virus ، Naloxone ، Vaccine formulation

نویسندگان

Melika Haghighi

Advanced Therapy Medicinal Product (ATMP) Department, Breast Cancer Research Center, Motamed Cancer Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran

Akbar Khorasani

Department of FMD Vaccine Production, Razi Vaccine & Serum Research Institute, Agricultural Research, Education & Extension Organization (AREEO), Karaj, Iran

Pegah Karimi

Advanced Therapy Medicinal Product (ATMP) Department, Breast Cancer Research Center, Motamed Cancer Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran

Mehdi Mahdavi

Advanced Therapy Medicinal Product (ATMP) Department, Breast Cancer Research Center, Motamed Cancer Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran

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