Evidence map›Paper›PMID 30476132›Full record

ArticleThe Journal of infectious diseases2019

Anti-OspA DNA-Encoded Monoclonal Antibody Prevents Transmission of Spirochetes in Tick Challenge Providing Sterilizing Immunity in Mice.

Yang Wang, Rianne Esquivel, Seleeke Flingai, Zachary A Schiller, Aurélie Kern, Sangya Agarwal, Jacqueline Chu, Ami Patel, Katherine Sullivan, Megan C Wise and 4 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Protection againstHuman vaccines & immunotherapeutics · 2020
    Article
  9. Article
  10. DNA vaccines: prime time is now.Current opinion in immunology · 2020
    Review
  11. In Vivo Delivery of Nucleic Acid-Encoded Monoclonal Antibodies.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2020
    Review
  12. 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

14 authors.

Yang WangMassBiologics of University of Massachusetts Medical School, Boston.
Rianne EsquivelVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Seleeke FlingaiVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Zachary A SchillerMassBiologics of University of Massachusetts Medical School, Boston.
Aurélie KernSackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts.
Sangya AgarwalVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Jacqueline ChuVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Ami PatelVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Katherine SullivanMassBiologics of University of Massachusetts Medical School, Boston.
Megan C WiseInovio Pharmaceuticals, Plymouth Meeting, Pennsylvania.
Kate E BroderickInovio Pharmaceuticals, Plymouth Meeting, Pennsylvania.
Linden HuSackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts.
David B WeinerVaccine and Immunotherapy Center, Wistar Institute, Philadelphia, Pennsylvania.
Mark S KlempnerMassBiologics of University of Massachusetts Medical School, Boston.

Funding

University of Massachusetts Center for Clinical Science and Translational SupplementUL1TR001453 · NCATS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2015 to 2024
$39.0M
Training in Emerging Infectious DiseasesT32AI055400 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI CHERRY, SARA, HENSLEY, SCOTT ERIC · 2003 to 2022
$4.4M
NCATS NIH HHS UL1 TR001453NIAID NIH HHS T32 AI055400
6 · The paper itself

Abstract

We recently developed anti-OspA human immunoglobulin G1 monoclonal antibodies (HuMAbs) that are effective in preventing Borrelia transmission from ticks in a murine model. Here, we investigated a novel approach of DNA-mediated gene transfer of HuMAbs that provide protection against Lyme disease. Plasmid DNA-encoded anti-OspA HuMAbs inoculated in mice achieved a serum antibody concentration of >6 μg/mL. Among mice injected with DNA-encoded monoclonal antibodies, 75%-77% were protected against an acute challenge by Borrelia-infected ticks. Our results represent the first demonstration of employing DNA transfer as a delivery system for antibodies that block transmission of Borrelia in animal models.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedAntigens, SurfaceBacterial Outer Membrane ProteinsBacterial VaccinesBorrelia burgdorferiDNA, BacterialFemaleHEK293 CellsHumansLipoproteinsLyme DiseaseMiceMice, Inbred C3HMice, SCIDPlasmidsAntibodies, Monoclonal, HumanizedAntigens, SurfaceBacterial Outer Membrane ProteinsBacterial VaccinesDNA, BacterialLipoproteinsOspA proteinDMAbhuman monoclonal antibodyLyme diseaseOspA

Identifiers

PMID30476132
PMCPMC6420172

What OpenQuestion holds

Textmetadata
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.