Evidence map›Paper›PMID 34329335›Full record

ArticlePloS one2021

Attenuating nicotine's effects with high affinity human anti-nicotine monoclonal antibodies.

Michael D Raleigh, Nicola Beltraminelli, Stephanie Fallot, Mark G LeSage, Amy Saykao, Paul R Pentel, Steve Fuller, Thomas Thisted, Zuzanna Biesova, Stephen Horrigan and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. 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 5 institutions in 1 country.

Michael D RaleighHennepin Healthcare Research Institute, Minneapolis, Minnesota, United States of America.ORCID 0000-0002-9715-6962
Nicola BeltraminelliBlink Biomedical, Marseille, France.
Stephanie FallotBlink Biomedical, Marseille, France.
Mark G LeSageHennepin Healthcare Research Institute, Minneapolis, Minnesota, United States of America.
Amy SaykaoHennepin Healthcare Research Institute, Minneapolis, Minnesota, United States of America.
Paul R PentelHennepin Healthcare Research Institute, Minneapolis, Minnesota, United States of America.
Steve FullerNic•mAb Strategic Alliance, San Diego, California, United States of America.
Thomas ThistedNic•mAb Strategic Alliance, San Diego, California, United States of America.
Zuzanna BiesovaAntidote Therapeutics, Inc., Woodbine, Maryland, United States of America.
Stephen HorriganNoble Life Sciences, Woodbine, Maryland, United States of America.
Darryl SampeyNic•mAb Strategic Alliance, San Diego, California, United States of America.
Bin ZhouNic•mAb Strategic Alliance, San Diego, California, United States of America.
Matthew W KalnikNic•mAb Strategic Alliance, San Diego, California, United States of America.
Hennepin Healthcare Research Institute · USBioFactura (United States) · USNoble Life Sciences (United States) · USScripps Research Institute · USUniversity of Minnesota · US

Funding

Lead Optimization and Preclinical Development of Human Nicotine-Specific mAbsR01DA038877 · NIDA · ANTIDOTE THERAPEUTICS, INC. · PI KALNIK, MATTHEW W · 2014 to 2016
$8.5M
NIDA NIH HHS R01 DA038877
6 · The paper itself

Abstract

Use of nicotine-specific monoclonal antibodies (mAbs) to sequester and reduce nicotine distribution to brain has been proposed as a therapeutic approach to treat nicotine addiction (the basis of tobacco use disorder). A series of monoclonal antibodies with high affinity for nicotine (nic•mAbs) was isolated from B-cells of vaccinated smokers. Genes encoding 32 unique nicotine binding antibodies were cloned, and the mAbs expressed and tested by surface plasmon resonance to determine their affinity for S-(-)-nicotine. The highest affinity nic•mAbs had binding affinity constants (KD) between 5 and 67 nM. The 4 highest affinity nic•mAbs were selected to undergo additional secondary screening for antigen-specificity, protein properties (including aggregation and stability), and functional in vivo studies to evaluate their capacity for reducing nicotine distribution to brain in rats. The 2 most potent nic•mAbs in single-dose nicotine pharmacokinetic experiments were further tested in a dose-response in vivo study. The most potent lead, ATI-1013, was selected as the lead candidate based on the results of these studies. Pretreatment with 40 and 80 mg/kg ATI-1013 reduced brain nicotine levels by 56 and 95%, respectively, in a repeated nicotine dosing experiment simulating very heavy smoking. Nicotine self-administration was also significantly reduced in rats treated with ATI-1013. A pilot rat 30-day repeat-dose toxicology study (4x200mg/kg ATI-1013) in the presence of nicotine indicated no drug-related safety concerns. These data provide evidence that ATI-1013 could be a potential therapy for the treatment of nicotine addiction.

Indexed as

Antibodies, MonoclonalAntibody AffinityNicotineTobacco Use DisorderAnimalsAntigen-Antibody ComplexBrainHumansRatsRats, Sprague-DawleyAntibodies, MonoclonalAntigen-Antibody ComplexNicotine

Identifiers

PMID34329335
PMCPMC8323890
OpenAlexW3183824930

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.