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Peptide-Based Vaccines for Tuberculosis

Overview
Journal Front Immunol
Date 2022 Feb 17
PMID 35173740
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Abstract

Tuberculosis (TB) is an infectious disease caused by . As a result of the coronavirus disease 2019 (COVID-19) pandemic, the global TB mortality rate in 2020 is rising, making TB prevention and control more challenging. Vaccination has been considered the best approach to reduce the TB burden. Unfortunately, BCG, the only TB vaccine currently approved for use, offers some protection against childhood TB but is less effective in adults. Therefore, it is urgent to develop new TB vaccines that are more effective than BCG. Accumulating data indicated that peptides or epitopes play essential roles in bridging innate and adaptive immunity and triggering adaptive immunity. Furthermore, innovations in bioinformatics, immunoinformatics, synthetic technologies, new materials, and transgenic animal models have put wings on the research of peptide-based vaccines for TB. Hence, this review seeks to give an overview of current tools that can be used to design a peptide-based vaccine, the research status of peptide-based vaccines for TB, protein-based bacterial vaccine delivery systems, and animal models for the peptide-based vaccines. These explorations will provide approaches and strategies for developing safer and more effective peptide-based vaccines and contribute to achieving the WHO's End TB Strategy.

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References
1.
Liang Y, Bai X, Zhang J, Song J, Yang Y, Yu Q . Ag85A/ESAT-6 chimeric DNA vaccine induces an adverse response in tuberculosis-infected mice. Mol Med Rep. 2016; 14(2):1146-52. PMC: 4940052. DOI: 10.3892/mmr.2016.5364. View

2.
Chatterjee N, Ojha R, Khatoon N, Prajapati V . Scrutinizing Mycobacterium tuberculosis membrane and secretory proteins to formulate multiepitope subunit vaccine against pulmonary tuberculosis by utilizing immunoinformatic approaches. Int J Biol Macromol. 2018; 118(Pt A):180-188. DOI: 10.1016/j.ijbiomac.2018.06.080. View

3.
Fisseha M, Chen P, Brandt B, Kijek T, Moran E, Zollinger W . Characterization of native outer membrane vesicles from lpxL mutant strains of Neisseria meningitidis for use in parenteral vaccination. Infect Immun. 2005; 73(7):4070-80. PMC: 1168616. DOI: 10.1128/IAI.73.7.4070-4080.2005. View

4.
Gong W, Liang Y, Mi J, Xue Y, Wang J, Wang L . A peptide-based vaccine ACP derived from antigens of Mycobacterium tuberculosis induced Th1 response but failed to enhance the protective efficacy of BCG in mice. Indian J Tuberc. 2022; 69(4):482-495. DOI: 10.1016/j.ijtb.2021.08.016. View

5.
Chaudhuri R, Kulshreshtha D, Raghunandanan M, Ramachandran S . Integrative immunoinformatics for Mycobacterial diseases in R platform. Syst Synth Biol. 2014; 8(1):27-39. PMC: 3933634. DOI: 10.1007/s11693-014-9135-9. View