Evidence map›Paper›PMID 23396091›Full record

ArticlemAbs

Prophylactic and therapeutic testing of Nicotiana-derived RSV-neutralizing human monoclonal antibodies in the cotton rat model.

Larry Zeitlin, Ognian Bohorov, Natasha Bohorova, Andrew Hiatt, Do H Kim, Michael H Pauly, Jesus Velasco, Kevin J Whaley, Dale L Barnard, John T Bates and 3 more

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.5field-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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Plant-Based Systems for Producing Therapeutic Proteins: Current Status and Future Prospects.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Therapy for Argentine hemorrhagic fever in nonhuman primates with a humanized monoclonal antibody.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Monoclonal antibody therapy for Junin virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Rapid replacement of human respiratory syncytial virus A with the ON1 genotype having 72 nucleotide duplication in G gene.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2014
    Article
  19. Glycan variants of a respiratory syncytial virus antibody with enhanced effector function and in vivo efficacy.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  20. Review
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

13 authors at 6 institutions in 1 country.

Larry ZeitlinMapp Biopharmaceutical, Inc., San Diego, CA, USA. larry.zeitlin@mappbio.com
Ognian Bohorov
Natasha Bohorova
Andrew Hiatt
Do H Kim
Michael H Pauly
Jesus Velasco
Kevin J Whaley
Dale L Barnard
John T Bates
James E Crowe
Pedro A Piedra
Brian E Gilbert
Mapp Biopharmaceutical (United States) · USUniversity of California, San Diego · USBaylor College of Medicine · USNashville Oncology Associates · USSarepta Therapeutics (United States) · USVanderbilt University Medical Center · US

Funding

T CELL MEMORY TO VIRUSESR01AI030048 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHMED, RAFI · 1990 to 2022
$5.2M
T CELL MEMORY TO VIRUSESR37AI030048 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI · 2001 to 2010
$3.9M
A HUMAN MONOCLONAL COCKTAIL FOR RSV IMMUNOTHERAPYR41AI063681 · NIAID · MAPP BIOPHARMACEUTICAL, INC. · PI ZEITLIN, LARRY · 2006 to 2007
$587k
NIAID NIH HHS HHSN272201000004CNIAID NIH HHS HHSN272201000004INIAID NIH HHS N01 AI030048NIAID NIH HHS N01-AI-30048NIAID NIH HHS R41 AI063681NIAID NIH HHS R41AI063681
6 · The paper itself

Abstract

Severe lower respiratory tract infection in infants and small children is commonly caused by respiratory syncytial virus (RSV). Palivizumab (Synagis(®)), a humanized IgG1 monoclonal antibody (mAb) approved for RSV immunoprophylaxis in at-risk neonates, is highly effective, but pharmacoeconomic analyses suggest its use may not be cost-effective. Previously described potent RSV neutralizers (human Fab R19 and F2-5; human IgG RF-1 and RF-2) were produced in IgG format in a rapid and inexpensive Nicotiana-based manufacturing system for comparison with palivizumab. Both plant-derived (palivizumab-N) and commercial palivizumab, which is produced in a mouse myeloma cell line, showed protection in prophylactic (p < 0.001 for both mAbs) and therapeutic protocols (p < 0.001 and p < 0.05 respectively). The additional plant-derived human mAbs directed against alternative epitopes displayed neutralizing activity, but conferred less protection in vivo than palivizumab-N or palivizumab. Palivizumab remains one of the most efficacious RSV mAbs described to date. Production in plants may reduce manufacturing costs and improve the pharmacoeconomics of RSV immunoprophylaxis and therapy.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingDisease Models, AnimalHumansNicotianaPalivizumabRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsSigmodontinaeTreatment OutcomeAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingPalivizumabantibodymonoclonalNicotianaprophylaxisRSVtherapy

Identifiers

PMID23396091
PMCPMC3893236
OpenAlexW2071760548

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.