In vitro and in vivo neutralization of Dengue virus by a single domain antibody

To alleviate the contribution of antibody dependent enhancement in DenV pathogenesis, we obtain a DenV neutralizing single domain antibody (sdAb) from an in-house constructed phage display library of camelid VHH. The anti-DenV sdAb specifically reacts with the envelope (E) protein of DenV with a Kd value of 2x108. Molecular dynamic simulations and docking analysis show that the sdAb interacts with the DenV(E) protein via domain II (EDII) and interferes with the virus internalization process. The anti-DenV(E) sdAb potently inhibits the infectivity of a DenV(E) protein expressing pseudovirus as well as that of a virulent DenV in vitro. A mouse adapted DenV2 induces 100% mortality in the infected IFNRKO mice, but the animals injected with the sdAb neutralized virus remain fully protected. Furthermore, the therapeutically administered anti-DenV(E) sdAb slows down the disease progression and enhances the survival of DenV infected animals. In conclusion, we report an anti-DenV(E) sdAb as a potential therapy to manage DenV pathogenesis.

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Publication Details

Journal
ImmunoHorizons
Published
2025-03-26
DOI
https://doi.org/10.1093/immhor/vlaf012
Citations
2
Primary Topic
Mosquito-borne diseases and control
Type
article
Field-Weighted Citation Impact
3.76

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article

In vitro and in vivo neutralization of Dengue virus by a single domain antibody

Surbhi Dahiya, Sharvan Sehrawat, Gaurav Kumar Bhati, Sudhakar Singh
2 citations
ImmunoHorizons
Mosquito-borne diseases and control
3.76
article

In vitro and in vivo neutralization of Dengue virus by a single domain antibody

Surbhi Dahiya, Sharvan Sehrawat, Gaurav Kumar Bhati, Sudhakar Singh
article en
2 citations

Abstract

To alleviate the contribution of antibody dependent enhancement in DenV pathogenesis, we obtain a DenV neutralizing single domain antibody (sdAb) from an in-house constructed phage display library of camelid VHH. The anti-DenV sdAb specifically reacts with the envelope (E) protein of DenV with a Kd value of 2x108. Molecular dynamic simulations and docking analysis show that the sdAb interacts with the DenV(E) protein via domain II (EDII) and interferes with the virus internalization process. The anti-DenV(E) sdAb potently inhibits the infectivity of a DenV(E) protein expressing pseudovirus as well as that of a virulent DenV in vitro. A mouse adapted DenV2 induces 100% mortality in the infected IFNRKO mice, but the animals injected with the sdAb neutralized virus remain fully protected. Furthermore, the therapeutically administered anti-DenV(E) sdAb slows down the disease progression and enhances the survival of DenV infected animals. In conclusion, we report an anti-DenV(E) sdAb as a potential therapy to manage DenV pathogenesis.

ImmunoHorizonsVol. 9(5)
Indian Institute of Science Education and Research Mohali (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Indian Institute of Science Education and Research Mohali
Good health and well-being
Openalex Percentile: Top 8%
Mosquito-borne diseases and control
3.76
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