Vaccine potential of ESAT-6 protein fused with consensus CD4+ T-cell epitopes of PE/PPE proteins against highly pathogenic Mycobacterium tuberculosis strain HN878

Soo Young Choi, Kee Woong Kwon, Hongmin Kim, Hong Hee Choi, Sung Jae Shin

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Pro-Glu/Pro-Pro-Glu (PE/PPE) family proteins in Mycobacterium tuberculosis (Mtb) are contributors to pathogenesis and immune evasion. These proteins have a unique structure in which the sequence is conserved. We investigated the vaccine potential of ESAT-6 fused with consensus CD4+ T-cell epitopes of PE/PPE proteins against highly pathogenic Mtb strain HN878 in a murine model. We selected consensus CD4+ T-cell epitopes of PE/PPE proteins by multiple alignments, investigated their IFN-γ response during Mtb infection, and produced their fused ESAT-6 vaccine antigens. Our results showed an increased immune response in PE/PPE peptide -ESAT-6 fusion protein immunization group compared to ESAT-6 only immunization group. After challenge with Mtb strain HN878, we observed that induced CD4+ T-cells secreted double-positive cytokine IL-2+/IFN-γ+, which is considered to be associated with protective T-cell immunity. Additionally, lower numbers of colony-forming units were observed in the spleen of fusion protein immunization groups than in those of single ESAT-6 group. Therefore, conjugation of consensus CD4+ T-cell epitopes in N terminus of PE/PPE to vaccine antigens could potentially increase the protective efficacy of subunit vaccine.

Original languageEnglish
Pages (from-to)2195-2201
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume503
Issue number4
DOIs
Publication statusPublished - 2018 Sep 18

Bibliographical note

Funding Information:
This research was supported by the International Research & Development Program through the National Research Foundation of Korea (NRF) funded by the Ministry of science, ICT & Future Planning ( NRF-2014K1A3A7A03075054 ).

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Fingerprint Dive into the research topics of 'Vaccine potential of ESAT-6 protein fused with consensus CD4<sup>+</sup> T-cell epitopes of PE/PPE proteins against highly pathogenic Mycobacterium tuberculosis strain HN878'. Together they form a unique fingerprint.

Cite this