Evidence map›Paper›PMID 36451809›Full record

ArticleFrontiers in immunology2022

A minimally-edited mouse model for infection with multiple SARS-CoV-2 strains.

Sandra Nakandakari-Higa, Roham Parsa, Bernardo S Reis, Renan V H de Carvalho, Luka Mesin, Hans-Heinrich Hoffmann, Juliana Bortolatto, Hiromi Muramatsu, Paulo J C Lin, Angelina M Bilate and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Adaptation of SARS-CoV-2 to ACE2Journal of virology · 2024
    Article
  6. 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.

Sandra Nakandakari-HigaLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Roham ParsaLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY, United States.
Bernardo S ReisLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY, United States.
Renan V H de CarvalhoLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Luka MesinLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Hans-Heinrich HoffmannLaboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, United States.
Juliana BortolattoLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Hiromi MuramatsuDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Paulo J C LinAcuitas Therapeutics, Vancouver, BC, Canada.
Angelina M BilateLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY, United States.
Charles M RiceLaboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, United States.
Norbert PardiDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Daniel MucidaLaboratory of Mucosal Immunology, The Rockefeller University, New York, NY, United States.
Gabriel D VictoraLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Maria Cecilia C CanessoLaboratory of Lymphocyte Dynamics, The Rockefeller University, New York, NY, United States.
Rockefeller University · USUniversity of Pennsylvania · USAcuitas Therapeutics (Canada) · CA

Funding

The longevity and nature of the anti-SARS-CoV-2 cellular and humoral immune responsesP01AI165075 · NIAID · ROCKEFELLER UNIVERSITY · PI BIENIASZ, PAUL D., BJORKMAN, PAMELA J · 2022 to 2023
$10.7M
Lipid nanoparticles as novel adjuvants inducing effective T follicular helper cell and humoral immune responsesR01AI153064 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Michela Locci, Norbert Pardi · 2020 to 2026
$4.2M
Development of Universal Influenza Virus Vaccines Using Nucleoside-Modified Messenger RNAR01AI146101 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PARDI, NORBERT · 2019 to 2023
$3.1M
NIAID NIH HHS R01 AI146101NIAID NIH HHS R01 AI153064
6 · The paper itself

Abstract

Efficient mouse models to study SARS-CoV-2 infection are critical for the development and assessment of vaccines and therapeutic approaches to mitigate the current pandemic and prevent reemergence of COVID-19. While the first generation of mouse models allowed SARS-CoV-2 infection and pathogenesis, they relied on ectopic expression and non-physiological levels of human angiotensin-converting enzyme 2 (hACE2). Here we generated a mouse model carrying the minimal set of modifications necessary for productive infection with multiple strains of SARS-CoV-2. Substitution of only three amino acids in the otherwise native mouse

Indexed as

COVID-19SARS-CoV-2Angiotensin-Converting Enzyme 2AnimalsDisease Models, AnimalHumansMicePandemicsAngiotensin-Converting Enzyme 2lung inflammationmemory B cellsmouse ACE2mRNA vaccineSARS-CoV-2

Identifiers

PMID36451809
PMCPMC9703079
OpenAlexW4308973713

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.