» Articles » PMID: 33191675

Bioengineering of Virus-like Particles for the Prevention or Treatment of Allergic Diseases

Overview
Date 2020 Nov 16
PMID 33191675
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Recent findings on the mechanism of allergen-specific immunotherapy (AIT) have revisited the role of immunoglobulin G (IgG) as the development of specific blocking IgG antibodies appeared critical for the successful suppression of T-helper 2 (Th2)-biased allergic responses. Consequently, any form of molecular AIT-promoting potent allergen-specific neutralizing antibodies would be preferred to conventional administration of allergen extracts. The potent immunogenicity of virus-like particles (VLPs) could be harnessed for that purpose. The particle size (20-200 nm) optimizes uptake by antigen-presenting cells as well as lymphatic trafficking. Moreover, the display of antigens in repetitive arrays promotes potent B cell activation for the development of sustained antibody responses. The presentation of self-antigens on the particle surface was even capable to break B cell tolerance. In this review, we describe the immunomodulatory properties of the 3 VLP-based strategies designed so far for the treatment of allergic disease: VLP packaged with CpG motifs as well as chimeric particles displaying pro-Th2/Th2 cytokines or allergens (full-length or B cell epitopes).

Citing Articles

Virus-like particle encapsulation of functional proteins: advances and applications.

Sun X, Lian Y, Tian T, Cui Z Theranostics. 2024; 14(19):7604-7622.

PMID: 39659581 PMC: 11626933. DOI: 10.7150/thno.103127.


Virus-like Particles as Vaccines for Allergen-Specific Therapy: An Overview of Current Developments.

Berreiros-Hortala H, Vilchez-Pinto G, Diaz-Perales A, Garrido-Arandia M, Tome-Amat J Int J Mol Sci. 2024; 25(13).

PMID: 39000536 PMC: 11242184. DOI: 10.3390/ijms25137429.


Cell and biomaterial delivery strategies to induce immune tolerance.

Scotland B, Shaw J, Dharmaraj S, Caprio N, Cottingham A, Lasola J Adv Drug Deliv Rev. 2023; 203:115141.

PMID: 37980950 PMC: 10842132. DOI: 10.1016/j.addr.2023.115141.


Suitability of potyviral recombinant virus-like particles bearing a complete food allergen for immunotherapy vaccines.

Pazos-Castro D, Margain C, Gonzalez-Klein Z, Amores-Borge M, Yuste-Calvo C, Garrido-Arandia M Front Immunol. 2022; 13:986823.

PMID: 36159839 PMC: 9492988. DOI: 10.3389/fimmu.2022.986823.


Recent Advances in Allergen-Specific Immunotherapy in Humans: A Systematic Review.

Lee S, Shin Y, Kang S, Kim T, Lee S Immune Netw. 2022; 22(1):e12.

PMID: 35291653 PMC: 8901700. DOI: 10.4110/in.2022.22.e12.


References
1.
Hong S, Zhang Z, Liu H, Tian M, Zhu X, Zhang Z . B Cells Are the Dominant Antigen-Presenting Cells that Activate Naive CD4 T Cells upon Immunization with a Virus-Derived Nanoparticle Antigen. Immunity. 2018; 49(4):695-708.e4. DOI: 10.1016/j.immuni.2018.08.012. View

2.
Hammad H, Lambrecht B . Barrier Epithelial Cells and the Control of Type 2 Immunity. Immunity. 2015; 43(1):29-40. DOI: 10.1016/j.immuni.2015.07.007. View

3.
Chackerian B, Lenz P, Lowy D, Schiller J . Determinants of autoantibody induction by conjugated papillomavirus virus-like particles. J Immunol. 2002; 169(11):6120-6. DOI: 10.4049/jimmunol.169.11.6120. View

4.
Ward A, Wilson I . Insights into the trimeric HIV-1 envelope glycoprotein structure. Trends Biochem Sci. 2015; 40(2):101-7. PMC: 4310573. DOI: 10.1016/j.tibs.2014.12.006. View

5.
Rohn T, Jennings G, Hernandez M, Grest P, Beck M, Zou Y . Vaccination against IL-17 suppresses autoimmune arthritis and encephalomyelitis. Eur J Immunol. 2006; 36(11):2857-67. DOI: 10.1002/eji.200636658. View