Evidence map›Paper›PMID 28387350›Full record

ArticleScientific reports2017

Recombinant Adeno-Associated Virus-Mediated Expression of Methamphetamine Antibody Attenuates Methamphetamine-Induced Hyperactivity in Mice.

Yun-Hsiang Chen, Kuo-Jen Wu, Kuang-Lun Wu, Kun-Lieh Wu, Ho-Min Tsai, Mao-Liang Chen, Yi-Wei Chen, Wei Hsieh, Chun-Ming Lin, Yun Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  6. Association between α1-antitrypsin and acute coronary syndrome.Experimental and therapeutic medicine · 2020
    Article
  7. Neuronal Activation Stimulates Cytomegalovirus Promoter-Driven Transgene Expression.Molecular therapy. Methods & clinical development · 2019
    Article
  8. Article
  9. 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

10 authors at 5 institutions in 1 country.

Yun-Hsiang ChenDepartment of Life Science, Fu-Jen Catholic University, New Taipei City, Taiwan.
Kuo-Jen WuCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Kuang-Lun WuCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Kun-Lieh WuDepartment of Electrical Engineering of I-Shou University, Kaohsiung, Taiwan.
Ho-Min TsaiCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Mao-Liang ChenDepartment of Research, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City, Taiwan.
Yi-Wei ChenDepartment of Life Science, Fu-Jen Catholic University, New Taipei City, Taiwan.
Wei HsiehDepartment of Life Science, Fu-Jen Catholic University, New Taipei City, Taiwan.
Chun-Ming LinDepartment of Microbiology, Soochow University, Taipei, Taiwan.
Yun WangCenter for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
National Health Research Institutes · TWI-Shou University · TWFu Jen Catholic University · TWSoochow University · TWTaipei Tzu Chi Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methamphetamine (Meth) is one of the most frequently abused drugs worldwide. Recent studies have indicated that antibodies with high affinity for Meth reduce its pharmacological effects. The purpose of this study was to develop a technique for virus-based passive immunization against Meth effects. We generated a recombinant adeno-associated virus serotype-8 vector (AAV-MethAb) carrying the gene for a Meth-specific monoclonal antibody (MethAb). Infection of 293 cells with AAV-MethAb resulted in the expression and secretion of antibodies which bind to Meth. The viral vector was then examined in adult ICR mice. Systemic administration of AAV-MethAb resulted in long-term expression of MethAb in the serum for up to 29 weeks. Serum collected from the animals receiving AAV-MethAb retained a high specificity for (+)-Meth. Animals were challenged with Meth five weeks after viral injection. Meth levels in the brain and serum were reduced while Meth-induced locomotor activity was significantly attenuated. In conclusion, AAV-MethAb administration effectively depletes Meth from brain and serum while reducing the behavioral response to Meth, and thus is a potential therapeutic approach for Meth abuse.

Indexed as

Amphetamine-Related DisordersAnimalsAntibodies, NeutralizingDependovirusHEK293 CellsHumansHyperkinesisImmunization, PassiveMaleMethamphetamineMiceMice, Inbred ICRAntibodies, NeutralizingMethamphetamine

Identifiers

PMID28387350
PMCPMC5384190
OpenAlexW2605055331

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.