Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs

Objective: To evaluate the effects of primary anti-dengue virus envelop protein domain 3 (DENV-ED3) antibodies on secondary heterotypic anti-DENV ED3 antibody responses and the status of anti-DENV antibody responses against multivalent DENV ED3s in mice. Methods: Four different DENV-ED3s were purifi...

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Main Authors: Md. Din Islam, Sanjida Yesmin, Tahmina Sharmin, Md. Ayoub Khan, Yutaka Kuroda, M. Monirul Islam
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Asian Pacific Journal of Tropical Medicine
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Online Access:https://journals.lww.com/10.4103/apjtm.apjtm_257_24
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author Md. Din Islam
Sanjida Yesmin
Tahmina Sharmin
Md. Ayoub Khan
Yutaka Kuroda
M. Monirul Islam
author_facet Md. Din Islam
Sanjida Yesmin
Tahmina Sharmin
Md. Ayoub Khan
Yutaka Kuroda
M. Monirul Islam
author_sort Md. Din Islam
collection DOAJ
description Objective: To evaluate the effects of primary anti-dengue virus envelop protein domain 3 (DENV-ED3) antibodies on secondary heterotypic anti-DENV ED3 antibody responses and the status of anti-DENV antibody responses against multivalent DENV ED3s in mice. Methods: Four different DENV-ED3s were purified and their biophysical characteristics were confirmed. Swiss albino mice aged 3-4 weeks were immunized with four different DENV-ED3s and the anti-ED3 IgG responses were determined by ELISA. Results: Firstly, the primary 1ED3-2ED3-3ED3 cross-reactive anti-DENV1 ED3 response boosted the secondary anti-2ED3 and anti-3ED3 antibody responses. In contrast, primary anti-2ED3 and anti-3ED3 antibodies neither had cross-recognition of 1ED3, nor had any effect on secondary anti-1ED3 response. Besides, the strict serospecificity of the anti-4ED3 sera did not affect other secondary anti-DENV ED3 responses. Secondly, 1ED3, 2ED3, and 3ED3 were co-dominantly immunogenic in trivalent ED3 formulations. However, the poorly immunogenic 4ED3 became almost non-immunogenic when injected after or together with 2ED3 and 3ED3, but showed slightly increased immunogenicity when injected with 1ED3, suggesting an adjuvanticity of 1ED3 on 4ED3’s immunogenicity. Conclusions: Although DENV1~4 ED3s share similar sequence homologies and structures, their immune induction potentials differ significantly in terms of immune magnitude, sero-specificity, and sero-cross-reactivity. Such intrinsic features of DENV1~4 ED3s may lead to ‘antigen interference’, limiting both the understanding of dengue etiology and the success of dengue vaccine development, which needs to neutralize all four DENV serotypes equivalently.
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spelling doaj-art-078691a5978e464b86cd763115cdc3882025-01-07T04:55:34ZengWolters Kluwer Medknow PublicationsAsian Pacific Journal of Tropical Medicine2352-41462024-12-01171255356210.4103/apjtm.apjtm_257_24Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVsMd. Din IslamSanjida YesminTahmina SharminMd. Ayoub KhanYutaka KurodaM. Monirul IslamObjective: To evaluate the effects of primary anti-dengue virus envelop protein domain 3 (DENV-ED3) antibodies on secondary heterotypic anti-DENV ED3 antibody responses and the status of anti-DENV antibody responses against multivalent DENV ED3s in mice. Methods: Four different DENV-ED3s were purified and their biophysical characteristics were confirmed. Swiss albino mice aged 3-4 weeks were immunized with four different DENV-ED3s and the anti-ED3 IgG responses were determined by ELISA. Results: Firstly, the primary 1ED3-2ED3-3ED3 cross-reactive anti-DENV1 ED3 response boosted the secondary anti-2ED3 and anti-3ED3 antibody responses. In contrast, primary anti-2ED3 and anti-3ED3 antibodies neither had cross-recognition of 1ED3, nor had any effect on secondary anti-1ED3 response. Besides, the strict serospecificity of the anti-4ED3 sera did not affect other secondary anti-DENV ED3 responses. Secondly, 1ED3, 2ED3, and 3ED3 were co-dominantly immunogenic in trivalent ED3 formulations. However, the poorly immunogenic 4ED3 became almost non-immunogenic when injected after or together with 2ED3 and 3ED3, but showed slightly increased immunogenicity when injected with 1ED3, suggesting an adjuvanticity of 1ED3 on 4ED3’s immunogenicity. Conclusions: Although DENV1~4 ED3s share similar sequence homologies and structures, their immune induction potentials differ significantly in terms of immune magnitude, sero-specificity, and sero-cross-reactivity. Such intrinsic features of DENV1~4 ED3s may lead to ‘antigen interference’, limiting both the understanding of dengue etiology and the success of dengue vaccine development, which needs to neutralize all four DENV serotypes equivalently.https://journals.lww.com/10.4103/apjtm.apjtm_257_24dengue viruses (denvs)denv sero-specificitydenv serotype-cross-talksprimary denv infectionssecondary denv infectionsmultivalent denv-ed3s
spellingShingle Md. Din Islam
Sanjida Yesmin
Tahmina Sharmin
Md. Ayoub Khan
Yutaka Kuroda
M. Monirul Islam
Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
Asian Pacific Journal of Tropical Medicine
dengue viruses (denvs)
denv sero-specificity
denv serotype-cross-talks
primary denv infections
secondary denv infections
multivalent denv-ed3s
title Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
title_full Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
title_fullStr Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
title_full_unstemmed Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
title_short Anti-DENV-ED3 antibody cross-talks generate immune interference among the four DENVs
title_sort anti denv ed3 antibody cross talks generate immune interference among the four denvs
topic dengue viruses (denvs)
denv sero-specificity
denv serotype-cross-talks
primary denv infections
secondary denv infections
multivalent denv-ed3s
url https://journals.lww.com/10.4103/apjtm.apjtm_257_24
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