Evidence map›Paper›PMID 23460798›Full record

ArticlePloS one2013

Partial MHC/neuroantigen peptide constructs: a potential neuroimmune-based treatment for methamphetamine addiction.

Jennifer M Loftis, Clare J Wilhelm, Arthur A Vandenbark, Marilyn Huckans

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  15. Neuroimmune basis of methamphetamine toxicity.International review of neurobiology · 2014
    Review
  16. Review
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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

4 authors at 2 institutions in 1 country.

Jennifer M LoftisResearch and Development, Portland VA Medical Center, Portland, Oregon, United States of America. loftisj@ohsu.edu
Clare J Wilhelm
Arthur A Vandenbark
Marilyn Huckans
Portland VA Medical Center · USOregon Health & Science University · US

Funding

Traditional Service Core [Translational Service Core (TSC)]P50DA018165 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI BELKNAP, JOHN K · 2006 to 2016
$13.0M
REGULATION OF EAE WITH RECOMBINANT TCR LIGANDSR01NS047661 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI VANDENBARK, ARTHUR A. · 2005 to 2014
$3.2M
Pre-clinical testing of a novel immunotherapy [recombinant T cell receptor ligandRC1DA028537 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI HUCKANS, MARILYN, LOFTIS, JENNIFER M · 2009 to 2010
$944k
Novel RTL treatment to promote brain repair and cognitive recovery following methR41DA029345 · NIDA · VIROGENOMICS, INC. · PI HUCKANS, MARILYN, LOFTIS, JENNIFER M · 2010 to 2010
$173k
NIDA NIH HHS P50 DA018165NIDA NIH HHS P50DA018165NIDA NIH HHS R41 DA029345NIDA NIH HHS R41DA029345NIDA NIH HHS RC1 DA028537NIDA NIH HHS RC1DA028537NINDS NIH HHS R01 NS047661
6 · The paper itself

Abstract

Relapse rates following current methamphetamine abuse treatments are very high (∼40-60%), and the neuropsychiatric impairments (e.g., cognitive deficits, mood disorders) that arise and persist during remission from methamphetamine addiction likely contribute to these high relapse rates. Pharmacotherapeutic development of medications to treat addiction has focused on neurotransmitter systems with only limited success, and there are no Food and Drug Administration approved pharmacotherapies for methamphetamine addiction. A growing literature shows that methamphetamine alters peripheral and central immune functions and that immune factors such as cytokines, chemokines, and adhesion molecules play a role in the development and persistence of methamphetamine induced neuronal injury and neuropsychiatric impairments. The objective of this study was to evaluate the efficacy of a new immunotherapy, partial MHC/neuroantigen peptide construct (RTL551; pI-A(b)/mMOG-35-55), in treating learning and memory impairments induced by repeated methamphetamine exposure. C57BL/6J mice were exposed to two different methamphetamine treatment regimens (using repeated doses of 4 mg/kg or 10 mg/kg, s.c.). Cognitive performance was assessed using the Morris water maze and CNS cytokine levels were measured by multiplex assay. Immunotherapy with RTL551 improved the memory impairments induced by repeated methamphetamine exposure in both mouse models of chronic methamphetamine addiction. Treatment with RTL551 also attenuated the methamphetamine induced increases in hypothalamic interleukin-2 (IL-2) levels. Collectively, these initial results indicate that neuroimmune targeted therapies, and specifically RTL551, may have potential as treatments for methamphetamine-induced neuropsychiatric impairments.

Indexed as

AnimalsAntigensCognitionCytokinesMajor Histocompatibility ComplexMaleMemory DisordersMethamphetamineMiceMice, Inbred C57BLNeuropeptidesRecombinant ProteinsSubstance-Related DisordersAntigensCytokinesMethamphetamineNeuropeptidesRecombinant Proteins

Identifiers

PMID23460798
PMCPMC3584080
OpenAlexW2002556051

What OpenQuestion holds

Textmetadata
LicenceCC0
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.