Evidence map›Paper›PMID 34552587›Full record

ArticleFrontiers in immunology2021

The Ability of Zika virus Intravenous Immunoglobulin to Protect From or Enhance Zika Virus Disease.

Amelia K Pinto, Mariah Hassert, Xiaobing Han, Douglas Barker, Trevor Carnelley, Emilie Branche, Tara L Steffen, E Taylor Stone, Elizabeth Geerling, Karla M Viramontes and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Microbiology spectrum · 2024
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
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

15 authors at 3 institutions in 2 countries.

Amelia K PintoDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
Mariah HassertDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
Xiaobing HanEmergent BioSolutions Canada Inc, Winnipeg, Canada.
Douglas BarkerEmergent BioSolutions Canada Inc, Winnipeg, Canada.
Trevor CarnelleyEmergent BioSolutions Canada Inc, Winnipeg, Canada.
Emilie BrancheLa Jolla Institute for Immunology, Center for Infectious Disease and Vaccine Research, La Jolla, CA, United States.
Tara L SteffenDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
E Taylor StoneDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
Elizabeth GeerlingDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
Karla M ViramontesLa Jolla Institute for Immunology, Center for Infectious Disease and Vaccine Research, La Jolla, CA, United States.
Cory NykiforukEmergent BioSolutions Canada Inc, Winnipeg, Canada.
Derek TothEmergent BioSolutions Canada Inc, Winnipeg, Canada.
Sujan ShrestaLa Jolla Institute for Immunology, Center for Infectious Disease and Vaccine Research, La Jolla, CA, United States.
Shantha KodihalliEmergent BioSolutions Canada Inc, Winnipeg, Canada.
James D BrienDepartment of Molecular Microbiology and Immunology, Saint Louis University, St Louis, MO, United States.
Emergent BioSolutions (Canada) · CASaint Louis University · USLa Jolla Institute for Immunology · US

Funding

Transcriptional and functional profiling of cross-reactive T cells to understand outcomes for the pathogen and host during heterologous infectionF31AI152460 · NIAID · SAINT LOUIS UNIVERSITY · PI HASSERT, MARIAH A · 2020 to 2021
$46k
NIAID NIH HHS F31 AI152460
6 · The paper itself

Abstract

The closely related flaviviruses, dengue and Zika, cause significant human disease throughout the world. While cross-reactive antibodies have been demonstrated to have the capacity to potentiate disease or mediate protection during flavivirus infection, the mechanisms responsible for this dichotomy are still poorly understood. To understand how the human polyclonal antibody response can protect against, and potentiate the disease in the context of dengue and Zika virus infection we used intravenous hyperimmunoglobulin (IVIG) preparations in a mouse model of the disease. Three IVIGs (ZIKV-IG, Control-Ig and Gamunex

Indexed as

Immunoglobulins, IntravenousAnimalsAntibodies, NeutralizingAntibodies, ViralCell LineCross ReactionsDisease Models, AnimalDose-Response Relationship, DrugHost-Pathogen InteractionsHumansMacrophagesMiceMice, KnockoutNeutralization TestsZika VirusZika Virus InfectionAntibodies, NeutralizingAntibodies, ViralImmunoglobulins, Intravenousanimal modelantibody dependent enhancementdengue virushyperimmunoglobulinZika virus

Identifiers

PMID34552587
PMCPMC8450494
OpenAlexW3197797285

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.