Evidence map›Paper›PMID 33408188›Full record

ArticleScience translational medicine2021

Neuronal delivery of antibodies has therapeutic effects in animal models of botulism.

Patrick M McNutt, Edwin J Vazquez-Cintron, Luis Tenezaca, Celinia A Ondeck, Kyle E Kelly, Mark Mangkhalakhili, James B Machamer, Christopher A Angeles, Elliot J Glotfelty, Jaclyn Cika and 5 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Neuroscience in prostate cancer.Prostate cancer and prostatic diseases · 2026
    Review
  2. Article
  3. Botulinum neurotoxin: from molecular pathogenesis to emerging countermeasures.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
    Review
  4. Equine botulism.Equine veterinary journal · 2026
    Review
  5. Article
  6. Gut mucin fucosylation dictates the entry of botulinum toxin complexes.bioRxiv : the preprint server for biology · 2025
    Article
  7. Targeted degradation of α-Synuclein using an evolved botulinum toxin protease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. The Degradation of Botulinum Neurotoxin Light Chains Using PROTACs.International journal of molecular sciences · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  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

15 authors at 6 institutions in 1 country.

Patrick M McNuttWake Forest School of Medicine, Wake Forest Institute for Regenerative Medicine, Winston-Salem, NC 27101, USA.ORCID 0000-0002-5703-4565
Edwin J Vazquez-CintronUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.ORCID 0000-0002-4397-3713
Luis TenezacaDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0002-2952-847X
Celinia A OndeckUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.ORCID 0000-0002-6437-3856
Kyle E KellyUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.
Mark MangkhalakhiliUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.ORCID 0000-0002-4868-7476
James B MachamerUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.ORCID 0000-0003-3532-8068
Christopher A AngelesDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0002-8160-0352
Elliot J GlotfeltyUnited States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.ORCID 0000-0001-5125-8720
Jaclyn CikaDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0003-2911-5648
Cesar H BenjumeaDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA.ORCID 0000-0003-2363-4893
Justin T WhitfieldCytoDel Inc., New York, NY 10016, USA.ORCID 0000-0001-5911-6655
Philip A BandDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Charles B ShoemakerDepartment of Infectious Diseases and Global Health, Cummings School of Veterinary Medicine at Tufts University, North Grafton, MA 01536, USA.ORCID 0000-0001-9738-1361
Konstantin IchtchenkoDepartment of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY 10016, USA. konstantin.ichtchenko@nyulangone.org.ORCID 0000-0002-2198-1325
United States Army · USNew York University · USCytoDel (United States) · USCity College of New York · USForest Institute · USTufts University · US

Funding

Novel therapeutic approaches to treatment of botulinum neurotoxin poisoning.R01AI093504 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Konstantin Ichtchenko · 2011 to 2026
$13.9M
Novel therapeutic approaches to treatment of botulinum neurotoxin poisoning.U01AI093504 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ICHTCHENKO, KONSTANTIN · 2019 to 2021
$3.4M
NIAID NIH HHS R01 AI093504NIAID NIH HHS U01 AI093504
6 · The paper itself

Abstract

Botulism is caused by a potent neurotoxin that blocks neuromuscular transmission, resulting in death by asphyxiation. Currently, the therapeutic options are limited and there is no antidote. Here, we harness the structural and trafficking properties of an atoxic derivative of botulinum neurotoxin (BoNT) to transport a function-blocking single-domain antibody into the neuronal cytosol where it can inhibit BoNT serotype A (BoNT/A1) molecular toxicity. Post-symptomatic treatment relieved toxic signs of botulism and rescued mice, guinea pigs, and nonhuman primates after lethal BoNT/A1 challenge. These data demonstrate that atoxic BoNT derivatives can be harnessed to deliver therapeutic protein moieties to the neuronal cytoplasm where they bind and neutralize intracellular targets in experimental models. The generalizability of this platform might enable delivery of antibodies and other protein-based therapeutics to previously inaccessible intraneuronal targets.

Indexed as

Botulinum Toxins, Type ABotulismSingle-Domain AntibodiesAnimalsGuinea PigsMiceModels, AnimalNeurotoxinsBotulinum Toxins, Type ANeurotoxinsSingle-Domain Antibodies

Identifiers

PMID33408188
PMCPMC8176400
OpenAlexW3118568467

What OpenQuestion holds

Textmetadata
LicenceTDM
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.