Evidence map›Paper›PMID 27413067›Full record

ArticleClinical and vaccine immunology : CVI2016

A Tetraspecific VHH-Based Neutralizing Antibody Modifies Disease Outcome in Three Animal Models of Clostridium difficile Infection.

Diane J Schmidt, Gillian Beamer, Jacqueline M Tremblay, Jennifer A Steele, Hyeun Bum Kim, Yaunkai Wang, Michele Debatis, Xingmin Sun, Elena A Kashentseva, Igor P Dmitriev and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Monoclonal Antibodies Targeting Bacterial Infections: A Broad Review of the Field.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. The state of play of rodent models for the study ofJournal of medical microbiology · 2024
    Review
  6. Article
  7. Immunization Strategies Against Clostridioides difficile.Advances in experimental medicine and biology · 2024
    Review
  8. Article
  9. Article
  10. Structure-guided design of a potentFrontiers in microbiology · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Neutralizing epitopes onFrontiers in immunology · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. A VFrontiers in plant science · 2021
    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

13 authors at 4 institutions in 3 countries.

Diane J SchmidtDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.ORCID http://orcid.org/0000-0001-6606-4398
Gillian BeamerDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Jacqueline M TremblayDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Jennifer A SteeleDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Hyeun Bum KimDepartment of Animal Resources Science, Dankook University, Cheonan, Republic of Korea.
Yaunkai WangSchool of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai Key Laboratory of Veterinary Biotechnology, Key Laboratory of Urban Agriculture (South) Ministry of Agriculture, Shanghai, People's Republic of China.
Michele DebatisDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Xingmin SunDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Elena A KashentsevaDepartment of Radiation Oncology, Washington University, St. Louis, Missouri, USA.
Igor P DmitrievDepartment of Radiation Oncology, Washington University, St. Louis, Missouri, USA.
David T CurielDepartment of Radiation Oncology, Washington University, St. Louis, Missouri, USA.
Charles B ShoemakerDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA.
Saul TziporiDepartment of Infectious Disease and Global Health, Cummings School of Veterinary Medicine, Tufts University, North Grafton, Massachusetts, USA saul.tzipori@tufts.edu.
Tufts University · USWashington University in St. Louis · USDankook University · KRShanghai Jiao Tong University · CN

Funding

Development of Vaccines against Clostridium difficile InfectionR01AI088748 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI FENG, HANPING, TZIPORI, SAUL R · 2010 to 2014
$3.1M
NIAID NIH HHS R01 AI088748
6 · The paper itself

Abstract

Clostridium difficile infection (CDI), a leading cause of nosocomial infection, is a serious disease in North America, Europe, and Asia. CDI varies greatly from asymptomatic carriage to life-threatening diarrhea, toxic megacolon, and toxemia. The incidence of community-acquired infection has increased due to the emergence of hypervirulent antibiotic-resistant strains. These new strains contribute to the frequent occurrence of disease relapse, complicating treatment, increasing hospital stays, and increasing morbidity and mortality among patients. Therefore, it is critical to develop new therapeutic approaches that bypass the development of antimicrobial resistance and avoid disruption of gut microflora. Here, we describe the construction of a single heteromultimeric VHH-based neutralizing agent (VNA) that targets the two primary virulence factors of Clostridium difficile, toxins A (TcdA) and B (TcdB). Designated VNA2-Tcd, this agent has subnanomolar toxin neutralization potencies for both C. difficile toxins in cell assays. When given systemically by parenteral administration, VNA2-Tcd protected against CDI in gnotobiotic piglets and mice and to a lesser extent in hamsters. Protection from CDI was also observed in gnotobiotic piglets treated by gene therapy with an adenovirus that promoted the expression of VNA2-Tcd.

Indexed as

AdenoviridaeAnimalsAntibodies, BacterialAntibodies, NeutralizingAntitoxinsBacterial ProteinsBacterial ToxinsClostridioides difficileClostridium InfectionsDisease Models, AnimalDrug CarriersDrug Evaluation, PreclinicalEnterotoxinsGenetic TherapyMesocricetusMice, Inbred C57BLAntibodies, BacterialAntibodies, NeutralizingAntitoxinsBacterial ProteinsBacterial ToxinsDrug CarriersEnterotoxinstcdA protein, Clostridium difficiletoxB protein, Clostridium difficile

Identifiers

PMID27413067
PMCPMC5014919
OpenAlexW2474833575

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.