» Articles » PMID: 37323212

Recombinant Lactic Acid Bacteria As Promising Vectors for Mucosal Vaccination

Overview
Date 2023 Jun 16
PMID 37323212
Authors
Affiliations
Soon will be listed here.
Abstract

Lactic acid bacteria (LAB), a diverse family of gram-positive bacteria, has been proven effective in delivering varieties of therapeutic and prophylactic molecules such as antigens and cytokines. Featuring the properties of acid-resistant, high uptake into Peyer's patches, and superior capacity for inducing secretory IgA antibodies, LAB have good potential to be used as vaccine vectors for mucosal vaccination. Mucosal immunization enables both mucosal and systemic immune responses, which are critical for resisting pathogens that invade the host through the mucosal surfaces. With the development of genetic engineering, LAB strains, primarily and have been exploited to express a range of heterologous antigens. Numerous studies have demonstrated that LAB mucosal vaccines can stimulate all arms of the immune system to provide adequate protection against pathogen infections. Additionally, several LAB-based human vaccines have entered the clinical trial studies, which suggest the great promise of LAB vaccines for new interventions in mucosal transport diseases. Herein, we will discuss the factors that influence the immunogenicity of LAB vaccines, including LAB strains, the location of antigens, and administration routes, and focus on the current strategies that have been reported for optimizing LAB vaccines.

Citing Articles

Maternal Milk Orchestrates the Development of Infant Gut Microbiota: Implications for Health and Future Research Directions.

Wang R, Sun S, Zhang Q, Wu G, Ren F, Chen J Research (Wash D C). 2025; 8:0558.

PMID: 39975576 PMC: 11836195. DOI: 10.34133/research.0558.


Effect of synbiotic supplementation on obesity and gut microbiota in obese adults: a double-blind randomized controlled trial.

Niu X, Zhang Q, Liu J, Zhao Y, Shang N, Li S Front Nutr. 2024; 11:1510318.

PMID: 39664910 PMC: 11633458. DOI: 10.3389/fnut.2024.1510318.


Recent advances in bacteria-based platforms for inflammatory bowel diseases treatment.

Lu J, Shen X, Li H, Du J Exploration (Beijing). 2024; 4(5):20230142.

PMID: 39439496 PMC: 11491310. DOI: 10.1002/EXP.20230142.


Physiochemically and Genetically Engineered Bacteria: Instructive Design Principles and Diverse Applications.

Lin X, Jiao R, Cui H, Yan X, Zhang K Adv Sci (Weinh). 2024; 11(30):e2403156.

PMID: 38864372 PMC: 11321697. DOI: 10.1002/advs.202403156.


Production of Promising Heat-Labile Enterotoxin (LT) B Subunit-Based Self-Assembled Bioconjugate Nanovaccines against Infectious Diseases.

Li C, Li J, Sun P, Li T, Yan X, Ye J Vaccines (Basel). 2024; 12(4).

PMID: 38675730 PMC: 11054625. DOI: 10.3390/vaccines12040347.


References
1.
Mielcarek N, Alonso S, Locht C . Nasal vaccination using live bacterial vectors. Adv Drug Deliv Rev. 2001; 51(1-3):55-69. DOI: 10.1016/s0169-409x(01)00168-5. View

2.
Li H, Piao D, Jiang T, Bok J, Cho C, Lee Y . Recombinant interleukin 6 with M cell-targeting moiety produced in Lactococcus lactis IL1403 as a potent mucosal adjuvant for peroral immunization. Vaccine. 2015; 33(16):1959-67. DOI: 10.1016/j.vaccine.2015.02.061. View

3.
Kim S, Jung D, Yang I, Kim J, Lee K, Nochi T . M cells expressing the complement C5a receptor are efficient targets for mucosal vaccine delivery. Eur J Immunol. 2011; 41(11):3219-29. DOI: 10.1002/eji.201141592. View

4.
Allaire J, Crowley S, Law H, Chang S, Ko H, Vallance B . The Intestinal Epithelium: Central Coordinator of Mucosal Immunity: (Trends in Immunology 39, 677-696, 2018). Trends Immunol. 2019; 40(2):174. DOI: 10.1016/j.it.2018.12.008. View

5.
Yu M, Qi R, Chen C, Yin J, Ma S, Shi W . Immunogenicity of recombinant Lactobacillus casei-expressing F4 (K88) fimbrial adhesin FaeG in conjunction with a heat-labile enterotoxin A (LTAK63) and heat-labile enterotoxin B (LTB) of enterotoxigenic Escherichia coli as an oral adjuvant in mice. J Appl Microbiol. 2016; 122(2):506-515. DOI: 10.1111/jam.13352. View