Liposomal delivery system/adjuvant for tuberculosis vaccine

Author:

Moradi Melika1,Vahedi Farzaneh2,Abbassioun Arian3,Ramezanpour Shahi Arash4,Sholeh Mohammad5,Taheri‐Anganeh Mortaza6,Dargahi Zahra1,Ghanavati Roya7,Khatami Seyyed Hossein8,Movahedpour Ahmad7ORCID

Affiliation:

1. Department of Microbiology, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

2. Department of Medical Biotechnology, School of Advanced Medical Sciences and Technologies Shiraz University of Medical Sciences Shiraz Iran

3. Department of Virology, Faculty of Veterinary Medicene University of Tehran Tehran Iran

4. Department of Veterinary Clinical Sciences, Poultry diseases and hygiene Resident, Faculty of Veterinary Medicine Shahrekord University Shahrekord Iran

5. Department of Bacteriology Pasteur Institute of Iran Tehran Iran

6. Cellular and Molecular Research Center, Cellular and Molecular Medicine Research Institute Urmia University of Medical Sciences Urmia Iran

7. Behbahan Faculty of Medical Sciences Behbahan Iran

8. Department of Clinical Biochemistry, School of Medicine Shahid Beheshti University of Medical Sciences Tehran Iran

Abstract

AbstractAs reported by the World Health Organization, about 10 million individuals were infected with tuberculosis (TB) worldwide. Moreover, approximately 1.5 million people died of TB, of which 214,000 were infected with HIV simultaneously. Due to the high infection rate, the need for effective TB vaccination is highly felt. Until now, various methodologies have been proposed for the development of a protein subunit vaccine for TB. These vaccines have shown higher protection than other vaccines, particularly the Bacillus culture vaccine. The delivery system and safety regulator are common characteristics of effective adjuvants in TB vaccines and the clinical trial stage. The present study investigates the current state of TB adjuvant research focusing on the liposomal adjuvant system. Based on our findings, the liposomal system is a safe and efficient adjuvant from nanosize to microsize for vaccinations against TB, other intracellular infections, and malignancies. Clinical studies can provide valuable feedback for developing novel TB adjuvants, which ultimately enhance the impact of adjuvants on next‐generation TB vaccines.

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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