Evidence map›Paper›PMID 30631063›Full record

ArticleNature communications2019

Post-exposure immunotherapy for two ebolaviruses and Marburg virus in nonhuman primates.

Jennifer M Brannan, Shihua He, Katie A Howell, Laura I Prugar, Wenjun Zhu, Hong Vu, Sergey Shulenin, Shweta Kailasan, Henna Raina, Gary Wong and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Marburg and Sudan virus outbreaks: are we any closer to a pan-filovirus vaccine?Tropical diseases, travel medicine and vaccines · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Pseudotyped Viruses for Marburgvirus and Ebolavirus.Advances in experimental medicine and biology · 2023
    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

19 authors at 4 institutions in 2 countries.

Jennifer M BrannanUS Army Medical Research Institute of Infectious Diseases, 1425 Porter St, Frederick, MD, 21702, USA.
Shihua HeSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Katie A HowellIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.ORCID http://orcid.org/0000-0003-3110-7022
Laura I PrugarUS Army Medical Research Institute of Infectious Diseases, 1425 Porter St, Frederick, MD, 21702, USA.
Wenjun ZhuSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Hong VuIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.
Sergey ShuleninIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.
Shweta KailasanIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.
Henna RainaIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.
Gary WongSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Md Niaz RahimSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Logan BanadygaSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Kevin TierneySpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada.
Xuelian ZhaoDepartment of Microbiology and Immunology, University of Maryland School of Medicine, 685 West Baltimore Street, Baltimore, MD, 21201, USA.ORCID http://orcid.org/0000-0003-2964-3184
Yuxing LiDepartment of Microbiology and Immunology, University of Maryland School of Medicine, 685 West Baltimore Street, Baltimore, MD, 21201, USA.
Frederick W HoltsbergIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA.
John M DyeUS Army Medical Research Institute of Infectious Diseases, 1425 Porter St, Frederick, MD, 21702, USA. john.m.dye1.civ@mail.mil.
Xiangguo QiuSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, 1015 Arlington Street, Winnipeg, MB, R3E 3R2, Canada. xiangguo.qiu@canada.ca.
M Javad AmanIntegrated BioTherapeutics, Inc., 4 Research Court, Suite 300, Rockville, MD, 20850, USA. javad@integratedbiotherapeutics.com.
Integrated BioTherapeutics (United States) · USPublic Health Agency of Canada · CAUnited States Army Medical Research Institute of Infectious Diseases · USUniversity of Maryland, Baltimore · US

Funding

High-resolution definition of B cell responses to HIV Env for immunogen designR01AI102766 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI LI, YUXING · 2013 to 2024
$6.6M
Evolution of anti-filovirus B cell responses and mechanisms of protectionR01AI126587 · NIAID · INTEGRATED BIOTHERAPEUTICS, INC. · PI AMAN, M JAVAD, LI, YUXING · 2017 to 2021
$3.7M
Structure-guided redesign of monoclonal antibodies targeting conserved filovirus epitopesR43AI124765 · NIAID · INTEGRATED BIOTHERAPEUTICS, INC. · PI AMAN, M JAVAD · 2016 to 2016
$284k
NIAID NIH HHS R01 AI102766NIAID NIH HHS R01 AI126587NIAID NIH HHS R43 AI124765
6 · The paper itself

Abstract

The 2013-2016 Ebola virus (EBOV) disease epidemic demonstrated the grave consequences of filovirus epidemics in the absence of effective therapeutics. Besides EBOV, two additional ebolaviruses, Sudan (SUDV) and Bundibugyo (BDBV) viruses, as well as multiple variants of Marburg virus (MARV), have also caused high fatality epidemics. Current experimental EBOV monoclonal antibodies (mAbs) are ineffective against SUDV, BDBV, or MARV. Here, we report that a cocktail of two broadly neutralizing ebolavirus mAbs, FVM04 and CA45, protects nonhuman primates (NHPs) against EBOV and SUDV infection when delivered four days post infection. This cocktail when supplemented by the anti-MARV mAb MR191 exhibited 100% efficacy in MARV-infected NHPs. These findings provide a solid foundation for clinical development of broadly protective immunotherapeutics for use in future filovirus epidemics.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingEbolavirusFiloviridae InfectionsHost-Pathogen InteractionsImmunotherapyMarburgvirusPrimate DiseasesPrimatesTreatment OutcomeAntibodies, MonoclonalAntibodies, Neutralizing

Identifiers

PMID30631063
PMCPMC6328579
OpenAlexW2910219677

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.