A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients

The immune response to dengue virus (DENV) infection generates high levels of antibodies (Abs) against the DENV non-structural protein 1 (NS1), particularly in cases of secondary infection. Therefore, anti-NS1 Abs may play a role in severe dengue infections, possibly by interacting (directly or indi...

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Main Authors: Magot Diata Omokoko, Sabar Pambudi, Supranee Phanthanawiboon, Promsin Masrinoul, Chayanee Setthapramote, Tadahiro Sasaki, Motoki Kuhara, Pongrama Ramasoota, Akifumi Yamashita, Itaru Hirai, Kazuyoshi Ikuta, Takeshi Kurosu
Other Authors: Osaka University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/34094
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spelling th-mahidol.340942018-11-09T10:01:36Z A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients Magot Diata Omokoko Sabar Pambudi Supranee Phanthanawiboon Promsin Masrinoul Chayanee Setthapramote Tadahiro Sasaki Motoki Kuhara Pongrama Ramasoota Akifumi Yamashita Itaru Hirai Kazuyoshi Ikuta Takeshi Kurosu Osaka University Mahidol University Medical & Biological Laboratories Co, Ltd National Institute of Infectious Diseases University of the Ryukyus Immunology and Microbiology Medicine The immune response to dengue virus (DENV) infection generates high levels of antibodies (Abs) against the DENV non-structural protein 1 (NS1), particularly in cases of secondary infection. Therefore, anti-NS1 Abs may play a role in severe dengue infections, possibly by interacting (directly or indirectly) with host factors or regulating virus production. If it does play a role, NS1 may contain epitopes that mimic those epitopes of host molecules. Previous attempts to map immunogenic regions within DENV-NS1 were undertaken using mouse monoclonal Abs (MAbs). The aim of this study was to characterize the epitope regions of nine anti-NS1 human monoclonal Abs (HuMAbs) derived from six patients secondarily infected with DENV-2. These anti-NS1 HuMAbs were cross-reactive with DENV-1, -2, and -3 but not DENV-4. All HuMAbs bound a common epitope region located between amino acids 221 and 266 of NS1. This study is the first report to map a DENV-NS1 epitope region using anti-DENV MAbs derived from patients. Copyright © 2014 by The American Society of Tropical Medicine and Hygiene. 2018-11-09T02:26:59Z 2018-11-09T02:26:59Z 2014-01-01 Article American Journal of Tropical Medicine and Hygiene. Vol.91, No.1 (2014), 146-155 10.4269/ajtmh.13-0624 00029637 2-s2.0-84903897345 https://repository.li.mahidol.ac.th/handle/123456789/34094 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903897345&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Magot Diata Omokoko
Sabar Pambudi
Supranee Phanthanawiboon
Promsin Masrinoul
Chayanee Setthapramote
Tadahiro Sasaki
Motoki Kuhara
Pongrama Ramasoota
Akifumi Yamashita
Itaru Hirai
Kazuyoshi Ikuta
Takeshi Kurosu
A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
description The immune response to dengue virus (DENV) infection generates high levels of antibodies (Abs) against the DENV non-structural protein 1 (NS1), particularly in cases of secondary infection. Therefore, anti-NS1 Abs may play a role in severe dengue infections, possibly by interacting (directly or indirectly) with host factors or regulating virus production. If it does play a role, NS1 may contain epitopes that mimic those epitopes of host molecules. Previous attempts to map immunogenic regions within DENV-NS1 were undertaken using mouse monoclonal Abs (MAbs). The aim of this study was to characterize the epitope regions of nine anti-NS1 human monoclonal Abs (HuMAbs) derived from six patients secondarily infected with DENV-2. These anti-NS1 HuMAbs were cross-reactive with DENV-1, -2, and -3 but not DENV-4. All HuMAbs bound a common epitope region located between amino acids 221 and 266 of NS1. This study is the first report to map a DENV-NS1 epitope region using anti-DENV MAbs derived from patients. Copyright © 2014 by The American Society of Tropical Medicine and Hygiene.
author2 Osaka University
author_facet Osaka University
Magot Diata Omokoko
Sabar Pambudi
Supranee Phanthanawiboon
Promsin Masrinoul
Chayanee Setthapramote
Tadahiro Sasaki
Motoki Kuhara
Pongrama Ramasoota
Akifumi Yamashita
Itaru Hirai
Kazuyoshi Ikuta
Takeshi Kurosu
format Article
author Magot Diata Omokoko
Sabar Pambudi
Supranee Phanthanawiboon
Promsin Masrinoul
Chayanee Setthapramote
Tadahiro Sasaki
Motoki Kuhara
Pongrama Ramasoota
Akifumi Yamashita
Itaru Hirai
Kazuyoshi Ikuta
Takeshi Kurosu
author_sort Magot Diata Omokoko
title A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
title_short A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
title_full A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
title_fullStr A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
title_full_unstemmed A highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 Is a major epitope region in infected patients
title_sort highly conserved region between amino acids 221 and 266 of dengue virus non-structural protein 1 is a major epitope region in infected patients
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/34094
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