A cross-reactive antibody protects against Ross River virus musculoskeletal disease despite rapid neutralization escape in mice.
Alphavirus Infections
/ complications
Animals
Antibodies, Neutralizing
/ immunology
Antibodies, Viral
/ immunology
Cross Reactions
/ immunology
Female
Male
Mice
Mice, Inbred C57BL
Musculoskeletal Diseases
/ immunology
Receptors, Fc
/ physiology
Ross River virus
/ immunology
Viral Load
/ immunology
Virulence
Journal
PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
received:
26
03
2020
accepted:
25
06
2020
revised:
18
08
2020
pubmed:
8
8
2020
medline:
20
9
2020
entrez:
8
8
2020
Statut:
epublish
Résumé
Arthritogenic alphaviruses cause debilitating musculoskeletal disease and historically have circulated in distinct regions. With the global spread of chikungunya virus (CHIKV), there now is more geographic overlap, which could result in heterologous immunity affecting natural infection or vaccination. Here, we evaluated the capacity of a cross-reactive anti-CHIKV monoclonal antibody (CHK-265) to protect against disease caused by the distantly related alphavirus, Ross River virus (RRV). Although CHK-265 only moderately neutralizes RRV infection in cell culture, it limited clinical disease in mice independently of Fc effector function activity. Despite this protective phenotype, RRV escaped from CHK-265 neutralization in vivo, with resistant variants retaining pathogenic potential. Near the inoculation site, CHK-265 reduced viral burden in a type I interferon signaling-dependent manner and limited immune cell infiltration into musculoskeletal tissue. In a parallel set of experiments, purified human CHIKV immune IgG also weakly neutralized RRV, yet when transferred to mice, resulted in improved clinical outcome during RRV infection despite the emergence of resistant viruses. Overall, this study suggests that weakly cross-neutralizing antibodies can protect against heterologous alphavirus disease, even if neutralization escape occurs, through an early viral control program that tempers inflammation.
Identifiants
pubmed: 32760128
doi: 10.1371/journal.ppat.1008743
pii: PPATHOGENS-D-20-00591
pmc: PMC7433899
doi:
Substances chimiques
Antibodies, Neutralizing
0
Antibodies, Viral
0
Receptors, Fc
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1008743Subventions
Organisme : NIAID NIH HHS
ID : R01 AI127513
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI141436
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI114816
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI142790
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007281
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201400018C
Pays : United States
Déclaration de conflit d'intérêts
I have read the journal's policy and the authors of this manuscript have the following competing interests: M.S.D. is a consultant for Inbios, Eli Lilly, Vir Biotechnology, NGM Biopharmaceuticals, and Emergent BioSolutions and on the Scientific Advisory Board of Moderna. The Diamond laboratory at Washington University School of Medicine has received sponsored research agreements from Moderna and Emergent BioSolutions. J.E.C. has served as a consultant for Takeda Vaccines, Sanofi-Aventis U.S., Pfizer, and Novavax, is a member of the Scientific Advisory Boards of CompuVax and Meissa Vaccines and is Founder of IDBiologics. The Crowe laboratory at Vanderbilt University Medical Center has received sponsored research agreements from Moderna, Sanofi-Aventis U.S., and IDBiologics. L.H. was an employee of MacroGenics and has equity.
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