Evidence map›Paper›PMID 30107445›Full record

ArticleThe Journal of infectious diseases2018

Pan-Filovirus Serum Neutralizing Antibodies in a Subset of Congolese Ebolavirus Infection Survivors.

Matthew S Bramble, Nicole Hoff, Pavlo Gilchuk, Patrick Mukadi, Kai Lu, Reena H Doshi, Imke Steffen, Bradly P Nicholson, Allen Lipson, Neerja Vashist and 20 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Pseudotyped Viruses for Marburgvirus and Ebolavirus.Advances in experimental medicine and biology · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 12 institutions in 2 countries.

Matthew S BrambleDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
Nicole HoffDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
Pavlo GilchukVanderbilt Vaccine Center, and Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
Patrick MukadiInstitut National de Recherche Biomedicale, Kinshasa, Democratic Republic of the Congo.
Kai LuBlood Systems Research Institute, and Department of Laboratory Medicine, University of California, San Francisco.
Reena H DoshiDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
Imke SteffenBlood Systems Research Institute, and Department of Laboratory Medicine, University of California, San Francisco.
Bradly P NicholsonInstitute for Medical Research, Durham Veterans Affairs Medical Center, North Carolina.
Allen LipsonDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
Neerja VashistDepartment of Genetic Medicine Research, Children's Research Institute, Children's National Medical Center, Washington, District of Columbia.
Cyrus SinaiDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
D'andre SpencerDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
Garrard OlingerBoston University, School of Medicine, Department of Medicine, Massachusetts.
Emile Okitolonda WemakoyKinshasa School of Public Health, Kinshasa, Democratic Republic of the Congo.
Benoit Kebela IllungaDirection de la Lutte Contre les Maladies, Ministère de la Sante, Kinshasa, Democratic Republic of the Congo.
James PettittIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
James LogueIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Jonathan MarchandIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Justin VarugheseIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Richard S BennettIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Peter JahrlingIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Guy CavetAtreca, Inc, Redwood City.
Tito SerafiniAtreca, Inc, Redwood City.
Erica Ollmann SaphireSkaggs Institute for Chemical Biology, La Jolla, California.
Eric VilainDepartment of Genetic Medicine Research, Children's Research Institute, Children's National Medical Center, Washington, District of Columbia.
Jean Jacques Muyembe-TamfumInstitut National de Recherche Biomedicale, Kinshasa, Democratic Republic of the Congo.
Lisa E HenselyIntegrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Frederick, Maryland.
Graham SimmonsBlood Systems Research Institute, and Department of Laboratory Medicine, University of California, San Francisco.
James E CroweVanderbilt Vaccine Center, and Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
Anne W RimoinDepartment of Epidemiology, School of Public Health, University of California, Los Angeles.
University of California, Los Angeles · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversity of California, San Francisco · USChildren's National · USItasca Consultants (United States) · USMinistry of Public Health · CDNational Institute of Biomedical Research · CDVanderbilt University Medical Center · USBoston University · USDurham VA Medical Center · USScripps Research Institute · US

Funding

Integrated Research Facility at Fort DetrickZIDAI009006 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI COE, LINDA · 2009 to 2018
$341.7M
Supplemental Research Project (SRP)U19AI109711 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI GEISBERT, THOMAS WILLIAM · 2014 to 2018
$26.6M
University of California Launching Future Leaders in Global Health Research Training ProgramD43TW009343 · FIC · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CRAIG R COHEN, Sung-Jae Lee · 2017 to 2026
$14.7M
Serological prevalence of viral hemorrhagic fevers in Equatorial AfricaR21AI107420 · NIAID · VITALANT · PI SIMMONS, GRAHAM · 2014 to 2015
$438k
FIC NIH HHS D43 TW009343NIAID NIH HHS HHSN272200700016INIAID NIH HHS HHSN272201400058CNIAID NIH HHS U19 AI109711
6 · The paper itself

Abstract

One year after a Zaire ebolavirus (EBOV) outbreak occurred in the Boende Health Zone of the Democratic Republic of the Congo during 2014, we sought to determine the breadth of immune response against diverse filoviruses including EBOV, Bundibugyo (BDBV), Sudan (SUDV), and Marburg (MARV) viruses. After assessing the 15 survivors, 5 individuals demonstrated some degree of reactivity to multiple ebolavirus species and, in some instances, Marburg virus. All 5 of these survivors had immunoreactivity to EBOV glycoprotein (GP) and EBOV VP40, and 4 had reactivity to EBOV nucleoprotein (NP). Three of these survivors showed serologic responses to the 3 species of ebolavirus GPs tested (EBOV, BDBV, SUDV). All 5 samples also exhibited ability to neutralize EBOV using live virus, in a plaque reduction neutralization test. Remarkably, 3 of these EBOV survivors had plasma antibody responses to MARV GP. In pseudovirus neutralization assays, serum antibodies from a subset of these survivors also neutralized EBOV, BDBV, SUDV, and Taï Forest virus as well as MARV. Collectively, these findings suggest that some survivors of naturally acquired ebolavirus infection mount not only a pan-ebolavirus response, but also in less frequent cases, a pan-filovirus neutralizing response.

Indexed as

Antibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralAntibody SpecificityAntigens, ViralDemocratic Republic of the CongoEbolavirusGlycoproteinsHemorrhagic Fever, EbolaHumansLassa virusMarburgvirusNeutralization TestsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralAntigens, ViralGlycoproteins

Identifiers

PMID30107445
PMCPMC6217721
OpenAlexW2885519437

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.