Evidence map›Paper›PMID 34998466›Full record

ArticleCell host & microbe2022

Genotype-specific features reduce the susceptibility of South American yellow fever virus strains to vaccine-induced antibodies.

Denise Haslwanter, Gorka Lasso, Anna Z Wec, Nathália Dias Furtado, Lidiane Menezes Souza Raphael, Alexandra L Tse, Yan Sun, Stephanie Stransky, Núria Pedreño-Lopez, Carolina Argondizo Correia and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Frontiers in microbiology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 2 countries.

Denise HaslwanterDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, The Bronx, NY 10461, USA.
Gorka LassoDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, The Bronx, NY 10461, USA.
Anna Z WecAdimab, LLC, Lebanon, NH 03766, USA.
Nathália Dias FurtadoLaboratório de Biologia Molecular de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, 21040-360 Rio de Janeiro, Brazil.
Lidiane Menezes Souza RaphaelLaboratório de Biologia Molecular de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, 21040-360 Rio de Janeiro, Brazil.
Alexandra L TseDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, The Bronx, NY 10461, USA.
Yan SunDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Stephanie StranskyDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Núria Pedreño-LopezDepartment of Pathology, The George Washington University, Washington, DC 20037, USA.
Carolina Argondizo CorreiaLaboratório de Imunologia Clínica e Alergia, Faculdade de Medicina, Universidade de São Paulo, 01246-903 São Paulo, Brazil.
Zachary A BornholdtMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
Mrunal SakharkarAdimab, LLC, Lebanon, NH 03766, USA.
Vivian I Avelino-SilvaDepartamento de Moléstias Infecciosas e Parasitárias, Faculdade de Medicina, Universidade de São Paulo, 01246-903 São Paulo, Brazil.
Crystal L MoyerMapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
David I WatkinsDepartment of Pathology, The George Washington University, Washington, DC 20037, USA.
Esper G KallasDepartamento de Moléstias Infecciosas e Parasitárias, Faculdade de Medicina, Universidade de São Paulo, 01246-903 São Paulo, Brazil.
Simone SidoliDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Laura M WalkerAdimab, LLC, Lebanon, NH 03766, USA; Adagio Therapeutics Inc., Waltham, MA 02451, USA.
Myrna C BonaldoLaboratório de Biologia Molecular de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, 21040-360 Rio de Janeiro, Brazil. Electronic address: mbonaldo@ioc.fiocruz.br.
Kartik ChandranDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, The Bronx, NY 10461, USA. Electronic address: kartik.chandran@einsteinmed.edu.
Albert Einstein College of Medicine · USAdimab (United States) · USFundação Oswaldo Cruz · BRGeorge Washington University · USUniversidade de São Paulo · BRAssociação Brasileira de Alergia e Imunologia · BR

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
Dissecting the receptor-mediated infection mechanisms of hantavirusesR01AI132633 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHANDRAN, KARTIK · 2017 to 2021
$3.2M
Host-virus interactions in the control of filovirus entryR01AI134824 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHANDRAN, KARTIK · 2018 to 2021
$1.9M
How MeCP2 discriminates epigenetic marks is still a mysteryR01GM129350 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BRENOWITZ, MICHAEL D. · 2018 to 2021
$1.3M
Orbitrap Exploris 480 Basic SystemS10OD030286 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SIDOLI, SIMONE · 2021 to 2021
$600k
NIAID NIH HHS R01 AI132633NIAID NIH HHS R01 AI134824NIGMS NIH HHS R01 GM129350NIGMS NIH HHS T32 GM007288NIH HHS S10 OD030286
6 · The paper itself

Abstract

The resurgence of yellow fever in South America has prompted vaccination against the etiologic agent, yellow fever virus (YFV). Current vaccines are based on a live-attenuated YF-17D virus derived from a virulent African isolate. The capacity of these vaccines to induce neutralizing antibodies against the vaccine strain is used as a surrogate for protection. However, the sensitivity of genetically distinct South American strains to vaccine-induced antibodies is unknown. We show that antiviral potency of the polyclonal antibody response in vaccinees is attenuated against an emergent Brazilian strain. This reduction was attributable to amino acid changes at two sites in central domain II of the glycoprotein E, including multiple changes at the domain I-domain II hinge, which are unique to and shared among most South American YFV strains. Our findings call for a reevaluation of current approaches to YFV immunological surveillance in South America and suggest approaches for updating vaccines.

Indexed as

Yellow FeverYellow Fever VaccineAntibodies, ViralBrazilGenotypeHumansVaccines, AttenuatedYellow fever virusAntibodies, ViralVaccines, AttenuatedYellow Fever Vaccine17Dantibody responseemerging virusflavivirusglycoproteinimmunological responseneutralizing antibodiesSouth Americavaccineyellow fever virus

Identifiers

PMID34998466
PMCPMC10067022
OpenAlexW4220665760

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.