Implications of a highly divergent dengue virus strain for cross-neutralization, protection, and vaccine immunity.
Animals
Antibodies, Viral
/ blood
Antigens, Viral
/ immunology
Broadly Neutralizing Antibodies
/ blood
Cross Protection
Cross Reactions
Dengue
/ immunology
Dengue Vaccines
/ immunology
Dengue Virus
/ genetics
Female
Genotype
Humans
Immunization, Passive
Immunogenicity, Vaccine
Macaca mulatta
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Serogroup
Viral Envelope Proteins
/ chemistry
antibody
dengue
divergent
genotype
neutralization
pathogenesis
protection
serotype
Journal
Cell host & microbe
ISSN: 1934-6069
Titre abrégé: Cell Host Microbe
Pays: United States
ID NLM: 101302316
Informations de publication
Date de publication:
10 11 2021
10 11 2021
Historique:
received:
20
05
2021
revised:
15
08
2021
accepted:
10
09
2021
pubmed:
6
10
2021
medline:
28
1
2022
entrez:
5
10
2021
Statut:
ppublish
Résumé
Although divergent dengue viruses (DENVs) have been isolated in insects, nonhuman primates, and humans, their relationships to the four canonical serotypes (DENV 1-4) are poorly understood. One virus isolated from a dengue patient, DKE-121, falls between genotype and serotype levels of sequence divergence to DENV-4. To examine its antigenic relationship to DENV-4, we assessed serum neutralizing and protective activity. Whereas DENV-4-immune mouse sera neutralize DKE-121 infection, DKE-121-immune sera inhibit DENV-4 less efficiently. Passive transfer of DENV-4 or DKE-121-immune sera protects mice against homologous, but not heterologous, DENV-4 or DKE-121 challenge. Antigenic cartography suggests that DENV-4 and DKE-121 are related but antigenically distinct. However, DENV-4 vaccination confers protection against DKE-121 in nonhuman primates, and serum from humans immunized with a tetravalent vaccine neutralize DENV-4 and DKE-121 infection equivalently. As divergent DENV strains, such as DKE-121, may meet criteria for serotype distinction, monitoring their capacity to impact dengue disease and vaccine efficacy appears warranted.
Identifiants
pubmed: 34610295
pii: S1931-3128(21)00422-4
doi: 10.1016/j.chom.2021.09.006
pmc: PMC8595868
mid: NIHMS1741865
pii:
doi:
Substances chimiques
Antibodies, Viral
0
Antigens, Viral
0
Broadly Neutralizing Antibodies
0
Dengue Vaccines
0
Viral Envelope Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1634-1648.e5Subventions
Organisme : NIAID NIH HHS
ID : R01 AI125202
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI073755
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI164653
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI145012
Pays : United States
Organisme : NIAID NIH HHS
ID : 75N93019C00062
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007200
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007163
Pays : United States
Organisme : NIAID NIH HHS
ID : F30 AI152327
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI115577
Pays : United States
Organisme : NIH HHS
ID : U42 OD021458
Pays : United States
Organisme : NIH HHS
ID : P40 OD012217
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests M.S.D. is a consultant for Inbios, Vir Biotechnology, and Carnival Corporation and is on the scientific advisory boards of Moderna and Immunome. The Diamond Laboratory has received unrelated funding support in sponsored research agreements from Moderna, Vir Biotechnology, and Emergent BioSolutions. The Vasilakis laboratory has received unrelated funding support in sponsored research agreements from Public Health Vaccines.
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