Evidence map›Paper›PMID 34228761›Full record

ArticlePLoS pathogens2021

Early treatment with a combination of two potent neutralizing antibodies improves clinical outcomes and reduces virus replication and lung inflammation in SARS-CoV-2 infected macaques.

Koen K A Van Rompay, Katherine J Olstad, Rebecca L Sammak, Joseph Dutra, Jennifer K Watanabe, Jodie L Usachenko, Ramya Immareddy, Anil Verma, Yashavanth Shaan Lakshmanappa, Brian A Schmidt and 19 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
  7. Nonhuman primate models of pediatric viral diseases.Frontiers in cellular and infection microbiology · 2024
    Review
  8. Article
  9. Article
  10. Naturally-acquired and Vaccine-induced Human Monoclonal Antibodies tobioRxiv : the preprint server for biology · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

29 authors at 3 institutions in 1 country.

Koen K A Van RompayCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0002-7375-1337
Katherine J OlstadCalifornia National Primate Research Center, University of California, Davis, United States of America.
Rebecca L SammakCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0003-3271-0413
Joseph DutraDepartment of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, California, United States of America.ORCID 0000-0002-5553-5200
Jennifer K WatanabeCalifornia National Primate Research Center, University of California, Davis, United States of America.
Jodie L UsachenkoCalifornia National Primate Research Center, University of California, Davis, United States of America.
Ramya ImmareddyCalifornia National Primate Research Center, University of California, Davis, United States of America.
Anil VermaCenter for Immunology and Infectious Diseases, University of California, Davis, California, United States of America.
Yashavanth Shaan LakshmanappaCenter for Immunology and Infectious Diseases, University of California, Davis, California, United States of America.ORCID 0000-0002-7794-1963
Brian A SchmidtCenter for Immunology and Infectious Diseases, University of California, Davis, California, United States of America.ORCID 0000-0002-3405-4862
Jamin W RohCenter for Immunology and Infectious Diseases, University of California, Davis, California, United States of America.
Sonny R ElizaldiCenter for Immunology and Infectious Diseases, University of California, Davis, California, United States of America.ORCID 0000-0001-7464-8721
A Mark AllenCalifornia National Primate Research Center, University of California, Davis, United States of America.
Frauke MueckschLaboratory of Retrovirology, The Rockefeller University, New York, New York, United States of America.ORCID 0000-0002-0132-5101
Julio C C LorenziLaboratory of Molecular Immunology, The Rockefeller University, New York, New York, United States of America.ORCID 0000-0003-2492-3961
Sarah LockwoodCalifornia National Primate Research Center, University of California, Davis, United States of America.
Rachel E PollardSchool of Veterinary Medicine, University of California, Davis, California, United States of America.ORCID 0000-0003-2986-1827
JoAnn L YeeCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0002-5514-9836
Peter B NhamCalifornia National Primate Research Center, University of California, Davis, United States of America.
Amir ArdeshirCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0002-4330-4659
Jesse D DeereDepartment of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, California, United States of America.ORCID 0000-0002-2539-0338
Jean PattersonTranslational Research Section, Virology Branch, DMID/NIAID/NIH, Rockville, Maryland, United States of America.
Que DangPreclinical Research and Development Branch, Vaccine Research Program, DAIDS/NIAID/NIH, Rockville, Maryland, United States of America.
Theodora HatziioannouLaboratory of Retrovirology, The Rockefeller University, New York, New York, United States of America.ORCID 0000-0002-7889-0766
Paul D BieniaszLaboratory of Retrovirology, The Rockefeller University, New York, New York, United States of America.ORCID 0000-0002-2368-3719
Smita S IyerCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0002-8918-7005
Dennis J Hartigan-O'ConnorCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0003-4822-636X
Michel C NussenzweigLaboratory of Molecular Immunology, The Rockefeller University, New York, New York, United States of America.
J Rachel ReaderCalifornia National Primate Research Center, University of California, Davis, United States of America.ORCID 0000-0003-3864-6731
University of California, Davis · USRockefeller University · USHoward Hughes Medical Institute · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Investigating the Role of T cells in Age-related Neurodegeneration in HIV InfectionRF1AG061001 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI IYER, SWAMINATHAN SMITA, MORRISON, JOHN H · 2018 to 2022
$5.0M
Animal Models of Infectious Diseases Training ProgramT32AI060555 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI MCSORLEY, STEPHEN J · 2004 to 2025
$3.3M
Role of female genital mucosa associated CD4 T cells in vaccine-induced HIV susceptibilityR21AI143454 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI IYER, SWAMINATHAN SMITA · 2019 to 2020
$623k
NIAID NIH HHS R21 AI143454NIAID NIH HHS T32 AI060555NIA NIH HHS RF1 AG061001NIH HHS 1R21AI143454-02S1NIH HHS 3RF1AG061001NIH HHS P51 OD011107
6 · The paper itself

Abstract

There is an urgent need for effective therapeutic interventions against SARS-CoV-2, including new variants that continue to arise. Neutralizing monoclonal antibodies have shown promise in clinical studies. We investigated the therapeutic efficacy of a combination of two potent monoclonal antibodies, C135-LS and C144-LS that carry half-life extension mutations, in the rhesus macaque model of COVID-19. Twelve young adult macaques (three groups of four animals) were inoculated intranasally and intra-tracheally with a high dose of SARS-CoV-2 and 24 hours later, treated intravenously with a high (40 mg/kg) or low (12 mg/kg) dose of the C135-LS and C144-LS antibody combination, or a control monoclonal antibody. Animals were monitored for 7 days. Compared to the control animals, animals treated with either dose of the anti-SARS-CoV-2 antibodies showed similarly improved clinical scores, lower levels of virus replication in upper and lower respiratory tract, and significantly reduced interstitial pneumonia, as measured by comprehensive lung histology. In conclusion, this study provides proof-of-concept in support of further clinical development of these monoclonal antibodies against COVID-19 during early infection.

Indexed as

Virus ReplicationAnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralCOVID-19Disease Models, AnimalFemaleLungMacaca mulattaMaleMultivariate AnalysisRadiographyRespiratory SystemSARS-CoV-2Time FactorsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, Viral

Identifiers

PMID34228761
PMCPMC8284825
OpenAlexW3182861410

What OpenQuestion holds

Textmetadata
LicenceCC0
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.