Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB

BackgroundWith the increasing incidence of tuberculosis (TB) and the shortcomings of existing TB vaccines to prevent TB in adults, new TB vaccines need to be developed to address the complex TB epidemic.MethodThe dominant epitopes were screened from antigens to construct a novel epitope vaccine term...

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Main Authors: Peng Cheng, Fan Jiang, Guiyuan Wang, Jie Wang, Yong Xue, Liang Wang, Wenping Gong
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-01-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1102578/full
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author Peng Cheng
Peng Cheng
Fan Jiang
Guiyuan Wang
Guiyuan Wang
Jie Wang
Yong Xue
Liang Wang
Wenping Gong
author_facet Peng Cheng
Peng Cheng
Fan Jiang
Guiyuan Wang
Guiyuan Wang
Jie Wang
Yong Xue
Liang Wang
Wenping Gong
author_sort Peng Cheng
collection DOAJ
description BackgroundWith the increasing incidence of tuberculosis (TB) and the shortcomings of existing TB vaccines to prevent TB in adults, new TB vaccines need to be developed to address the complex TB epidemic.MethodThe dominant epitopes were screened from antigens to construct a novel epitope vaccine termed HP13138PB. The immune properties, structure, and function of HP13138PB were predicted and analyzed with bioinformatics and immunoinformatics. Then, the immune responses induced by the HP13138PB were confirmed by enzyme-linked immunospot assay (ELISPOT) and Th1/Th2/Th17 multi-cytokine detection kit.ResultThe HP13138PB vaccine consisted of 13 helper T lymphocytes (HTL) epitopes, 13 cytotoxic T lymphocytes (CTL) epitopes, and 8 B-cell epitopes. It was found that the antigenicity, immunogenicity, and solubility index of the HP13138PB vaccine were 0.87, 2.79, and 0.55, respectively. The secondary structure prediction indicated that the HP13138PB vaccine had 31% of α-helix, 11% of β-strand, and 56% of coil. The tertiary structure analysis suggested that the Z-score and the Favored region of the HP13138PB vaccine were -4.47 88.22%, respectively. Furthermore, the binding energies of the HP13138PB to toll-like receptor 2 (TLR2) was -1224.7 kcal/mol. The immunoinformatics and real-world experiments showed that the HP13138PB vaccine could induce an innate and adaptive immune response characterized by significantly higher levels of cytokines such as interferon-gamma (IFN-γ), tumor necrosis factor-α (TNF-α), interleukin-4 (IL-4), and IL-10.ConclusionThe HP13138PB is a potential vaccine candidate to prevent TB, and this study preliminarily evaluated the ability of the HP13138PB to generate an immune response, providing a precursor target for developing TB vaccines.
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spelling doaj.art-b7e33ac0791d45dd832f1181e3a8e70a2023-02-07T14:02:18ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-01-011410.3389/fimmu.2023.11025781102578Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PBPeng Cheng0Peng Cheng1Fan Jiang2Guiyuan Wang3Guiyuan Wang4Jie Wang5Yong Xue6Liang Wang7Wenping Gong8Tuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaDepartment of Geriatrics, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaThe Second Brigade of Cadet, Basic Medical School, Air Force Military Medical University, Xi’an, Shaanxi, ChinaTuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaHebei North University, Zhangjiakou, Hebei, ChinaTuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaTuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaDepartment of Geriatrics, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaTuberculosis Prevention and Control Key Laboratory/Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Senior Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, Beijing, ChinaBackgroundWith the increasing incidence of tuberculosis (TB) and the shortcomings of existing TB vaccines to prevent TB in adults, new TB vaccines need to be developed to address the complex TB epidemic.MethodThe dominant epitopes were screened from antigens to construct a novel epitope vaccine termed HP13138PB. The immune properties, structure, and function of HP13138PB were predicted and analyzed with bioinformatics and immunoinformatics. Then, the immune responses induced by the HP13138PB were confirmed by enzyme-linked immunospot assay (ELISPOT) and Th1/Th2/Th17 multi-cytokine detection kit.ResultThe HP13138PB vaccine consisted of 13 helper T lymphocytes (HTL) epitopes, 13 cytotoxic T lymphocytes (CTL) epitopes, and 8 B-cell epitopes. It was found that the antigenicity, immunogenicity, and solubility index of the HP13138PB vaccine were 0.87, 2.79, and 0.55, respectively. The secondary structure prediction indicated that the HP13138PB vaccine had 31% of α-helix, 11% of β-strand, and 56% of coil. The tertiary structure analysis suggested that the Z-score and the Favored region of the HP13138PB vaccine were -4.47 88.22%, respectively. Furthermore, the binding energies of the HP13138PB to toll-like receptor 2 (TLR2) was -1224.7 kcal/mol. The immunoinformatics and real-world experiments showed that the HP13138PB vaccine could induce an innate and adaptive immune response characterized by significantly higher levels of cytokines such as interferon-gamma (IFN-γ), tumor necrosis factor-α (TNF-α), interleukin-4 (IL-4), and IL-10.ConclusionThe HP13138PB is a potential vaccine candidate to prevent TB, and this study preliminarily evaluated the ability of the HP13138PB to generate an immune response, providing a precursor target for developing TB vaccines.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1102578/fulltuberculosisepitope vaccinesimmunoinformaticsimmune responsesbioinformatics
spellingShingle Peng Cheng
Peng Cheng
Fan Jiang
Guiyuan Wang
Guiyuan Wang
Jie Wang
Yong Xue
Liang Wang
Wenping Gong
Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
Frontiers in Immunology
tuberculosis
epitope vaccines
immunoinformatics
immune responses
bioinformatics
title Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
title_full Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
title_fullStr Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
title_full_unstemmed Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
title_short Bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate HP13138PB
title_sort bioinformatics analysis and consistency verification of a novel tuberculosis vaccine candidate hp13138pb
topic tuberculosis
epitope vaccines
immunoinformatics
immune responses
bioinformatics
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1102578/full
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