A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection

The effective protective HIV vaccine should elicit either protective antibodies or effective T cell response, or both. To improve the efficacy of HIV-1 vaccines, HLA polymorphism and HIV-1 diversity are 2 key factors to be considered for vaccine development. In this study, we expressed a recombinant...

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Main Authors: Yi Yang, Qing Zhu, Weilai Sun, Jingjing Guo, Xiuzhe Ning, Qiao Li, Yan Guo, Junfeng Li, Zhihua Kou, Yusen Zhou
Format: Article
Language:English
Published: Taylor & Francis Group 2017-06-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2017.1281488
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author Yi Yang
Qing Zhu
Weilai Sun
Jingjing Guo
Xiuzhe Ning
Qiao Li
Yan Guo
Junfeng Li
Zhihua Kou
Yusen Zhou
author_facet Yi Yang
Qing Zhu
Weilai Sun
Jingjing Guo
Xiuzhe Ning
Qiao Li
Yan Guo
Junfeng Li
Zhihua Kou
Yusen Zhou
author_sort Yi Yang
collection DOAJ
description The effective protective HIV vaccine should elicit either protective antibodies or effective T cell response, or both. To improve the efficacy of HIV-1 vaccines, HLA polymorphism and HIV-1 diversity are 2 key factors to be considered for vaccine development. In this study, we expressed a recombinant multi-epitope protein MEP1 which has the same amino acid sequence as a DNA vaccine for Chinese population in our previous report. We found that MEP1 alone could elicit moderate levels of humoral and cellular immune responses, but these responses could not provide protection from challenge with a recombinant virus rTTV-lucgag, which expresses Gag of HIV-1 CRF_07BC. Nevertheless, when MEP1 was immunized with aluminum adjuvant, both humoral and cellular immune responses were significantly increased, and they were protective against virus infection; meanwhile, MEP1 with aluminum not only elicited early (10 d post immunization) but also a long-term (at least 44 weeks post immunization) immune responses in BALB/c mice. These results suggested that MEP1 has the potential to be developed as an effective vaccine candidate, and that suitable adjuvant is necessary for this protein to generate protective immune responses.
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spelling doaj.art-577afe4d18e3446580c272fb4de0893b2023-09-25T11:02:54ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2017-06-011361466147410.1080/21645515.2017.12814881281488A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infectionYi Yang0Qing Zhu1Weilai Sun2Jingjing Guo3Xiuzhe Ning4Qiao Li5Yan Guo6Junfeng Li7Zhihua Kou8Yusen Zhou9State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologySchool of Laboratory Medicine and Life Science, Wenzhou Medical UniversityState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologyState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and EpidemiologySchool of Laboratory Medicine and Life Science, Wenzhou Medical UniversityThe effective protective HIV vaccine should elicit either protective antibodies or effective T cell response, or both. To improve the efficacy of HIV-1 vaccines, HLA polymorphism and HIV-1 diversity are 2 key factors to be considered for vaccine development. In this study, we expressed a recombinant multi-epitope protein MEP1 which has the same amino acid sequence as a DNA vaccine for Chinese population in our previous report. We found that MEP1 alone could elicit moderate levels of humoral and cellular immune responses, but these responses could not provide protection from challenge with a recombinant virus rTTV-lucgag, which expresses Gag of HIV-1 CRF_07BC. Nevertheless, when MEP1 was immunized with aluminum adjuvant, both humoral and cellular immune responses were significantly increased, and they were protective against virus infection; meanwhile, MEP1 with aluminum not only elicited early (10 d post immunization) but also a long-term (at least 44 weeks post immunization) immune responses in BALB/c mice. These results suggested that MEP1 has the potential to be developed as an effective vaccine candidate, and that suitable adjuvant is necessary for this protein to generate protective immune responses.http://dx.doi.org/10.1080/21645515.2017.1281488adjuvantaidsantibodyhiv-1memory immune responsesmulti-epitope proteint cell responses
spellingShingle Yi Yang
Qing Zhu
Weilai Sun
Jingjing Guo
Xiuzhe Ning
Qiao Li
Yan Guo
Junfeng Li
Zhihua Kou
Yusen Zhou
A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
Human Vaccines & Immunotherapeutics
adjuvant
aids
antibody
hiv-1
memory immune responses
multi-epitope protein
t cell responses
title A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
title_full A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
title_fullStr A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
title_full_unstemmed A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
title_short A recombinant multi-epitope protein MEP1 elicits efficient long-term immune responses against HIV-1 infection
title_sort recombinant multi epitope protein mep1 elicits efficient long term immune responses against hiv 1 infection
topic adjuvant
aids
antibody
hiv-1
memory immune responses
multi-epitope protein
t cell responses
url http://dx.doi.org/10.1080/21645515.2017.1281488
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