Evidence map›Paper›PMID 37402814›Full record

ArticleNature communications2023

An immunostimulatory glycolipid that blocks SARS-CoV-2, RSV, and influenza infections in vivo.

Moriya Tsuji, Manoj S Nair, Kazuya Masuda, Candace Castagna, Zhenlu Chong, Tamarand L Darling, Kuljeet Seehra, Youngmin Hwang, Ágata Lopes Ribeiro, Geovane Marques Ferreira and 8 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.5field-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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  10. IL-27 regulates the differentiation of follicular helper NKT cells via metabolic adaptation of mitochondria.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  15. Multi-viral defence in one sweep.Nature reviews. Microbiology · 2023
    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

18 authors at 4 institutions in 2 countries.

Moriya Tsuji *Aaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA. mt3432@cumc.columbia.edu.ORCID 0000-0001-8587-277X
Manoj S Nair *Aaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA.ORCID 0000-0002-5994-3957
Kazuya Masuda *Aaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA.ORCID 0000-0003-3041-1305
Candace Castagna *Institute of Comparative Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Zhenlu ChongDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Tamarand L DarlingDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Kuljeet SeehraDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Youngmin HwangColumbia Center for Human Development, Pulmonary Allergy & Critical Care Medicine, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Ágata Lopes RibeiroBasic and Applied Virology Laboratory, Department of Microbiology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Geovane Marques FerreiraBasic and Applied Virology Laboratory, Department of Microbiology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Laura CorredorInstitute of Comparative Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Jordana Grazziela Alves Coelho-Dos-ReisBasic and Applied Virology Laboratory, Department of Microbiology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Yukiko TsujiAaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Munemasa MoriColumbia Center for Human Development, Pulmonary Allergy & Critical Care Medicine, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Adrianus C M BoonDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID 0000-0002-4700-8224
Michael S DiamondDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.ORCID 0000-0002-8791-3165
Yaoxing HuangAaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA. yh3253@cumc.columbia.edu.ORCID 0000-0001-6270-1644
David D HoAaron Diamond AIDS Research Center, Columbia University Irving Medical Center, New York, NY, 10032, USA. dh2994@cumc.columbia.edu.ORCID 0000-0003-1627-149X
Aaron Diamond AIDS Research Center · USWashington University in St. Louis · USColumbia University Irving Medical Center · USUniversidade Federal de Minas Gerais · BR

Funding

COLLABORATIVE INFLUENZA VACCINE INNOVATION CENTER: UNIVERSAL INFLUENZA VACCINE RESEARCH75N93019C00051 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KRAMMER, FLORIAN · 2019 to 2025
$105.4M
NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
Emerging infections: surveillance, epidemiology and pathogenesisU01AI151810 · NIAID · WASHINGTON UNIVERSITY · PI Adrianus CM Boon, DAVID WANG · 2020 to 2026
$10.0M
Human antibody-based countermeasures against the Wuhan Coronavirus SARS-CoV-2R01AI157155 · NIAID · WASHINGTON UNIVERSITY · PI BARIC, RALPH S, CROWE, JAMES E · 2020 to 2024
$6.0M
NIAID NIH HHS 75N93019C00051NIAID NIH HHS 75N93021C00016NIAID NIH HHS R01 AI157155NIAID NIH HHS U01 AI151810
6 · The paper itself

Abstract

Prophylactic vaccines for SARS-CoV-2 have lowered the incidence of severe COVID-19, but emergence of viral variants that are antigenically distinct from the vaccine strains are of concern and additional, broadly acting preventive approaches are desirable. Here, we report on a glycolipid termed 7DW8-5 that exploits the host innate immune system to enable rapid control of viral infections in vivo. This glycolipid binds to CD1d on antigen-presenting cells and thereby stimulates NKT cells to release a cascade of cytokines and chemokines. The intranasal administration of 7DW8-5 prior to virus exposure significantly blocked infection by three different authentic variants of SARS-CoV-2, as well as by respiratory syncytial virus and influenza virus, in mice or hamsters. We also found that this protective antiviral effect is both host-directed and mechanism-specific, requiring both the CD1d molecule and interferon-[Formula: see text]. A chemical compound like 7DW8-5 that is easy to administer and cheap to manufacture may be useful not only in slowing the spread of COVID-19 but also in responding to future pandemics long before vaccines or drugs are developed.

Indexed as

COVID-19Influenza, HumanInfluenza VaccinesAnimalsCOVID-19 VaccinesHumansMiceSARS-CoV-2COVID-19 VaccinesInfluenza Vaccines

Identifiers

PMID37402814
PMCPMC10319732
OpenAlexW4383105850

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.