Protein-Based Adjuvants for Vaccines as Immunomodulators of the Innate and Adaptive Immune Response: Current Knowledge, Challenges, and Future Opportunities

New-generation vaccines, formulated with subunits or nucleic acids, are less immunogenic than classical vaccines formulated with live-attenuated or inactivated pathogens. This difference has led to an intensified search for additional potent vaccine adjuvants that meet safety and efficacy criteria a...

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Main Authors: Diego A. Díaz-Dinamarca (Author), Michelle L. Salazar (Author), Byron N. Castillo (Author), Augusto Manubens (Author), Abel E. Vasquez (Author), Fabián Salazar (Author), María Inés Becker (Author)
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Published: MDPI AG, 2022-08-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Diego A. Díaz-Dinamarca  |e author 
700 1 0 |a Michelle L. Salazar  |e author 
700 1 0 |a Byron N. Castillo  |e author 
700 1 0 |a Augusto Manubens  |e author 
700 1 0 |a Abel E. Vasquez  |e author 
700 1 0 |a Fabián Salazar  |e author 
700 1 0 |a María Inés Becker  |e author 
245 0 0 |a Protein-Based Adjuvants for Vaccines as Immunomodulators of the Innate and Adaptive Immune Response: Current Knowledge, Challenges, and Future Opportunities 
260 |b MDPI AG,   |c 2022-08-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14081671 
500 |a 1999-4923 
520 |a New-generation vaccines, formulated with subunits or nucleic acids, are less immunogenic than classical vaccines formulated with live-attenuated or inactivated pathogens. This difference has led to an intensified search for additional potent vaccine adjuvants that meet safety and efficacy criteria and confer long-term protection. This review provides an overview of protein-based adjuvants (PBAs) obtained from different organisms, including bacteria, mollusks, plants, and humans. Notably, despite structural differences, all PBAs show significant immunostimulatory properties, eliciting B-cell- and T-cell-mediated immune responses to administered antigens, providing advantages over many currently adopted adjuvant approaches. Furthermore, PBAs are natural biocompatible and biodegradable substances that induce minimal reactogenicity and toxicity and interact with innate immune receptors, enhancing their endocytosis and modulating subsequent adaptive immune responses. We propose that PBAs can contribute to the development of vaccines against complex pathogens, including intracellular pathogens such as <i>Mycobacterium tuberculosis</i>, those with complex life cycles such as <i>Plasmodium falciparum</i>, those that induce host immune dysfunction such as HIV, those that target immunocompromised individuals such as fungi, those with a latent disease phase such as <i>Herpes,</i> those that are antigenically variable such as SARS-CoV-2 and those that undergo continuous evolution, to reduce the likelihood of outbreaks. 
546 |a EN 
690 |a proteins 
690 |a adjuvants 
690 |a vaccines 
690 |a protein-based adjuvants 
690 |a Toll-like receptors 
690 |a C-type lectin receptors 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 8, p 1671 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/8/1671 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/a79ffd4ac05b43c49d295b339fb52ba5  |z Connect to this object online.