Evidence map›Paper›PMID 18388924›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2008

Reduced pathology and improved behavioral performance in Alzheimer's disease mice vaccinated with HSV amplicons expressing amyloid-beta and interleukin-4.

Maria E Frazer, Jennifer E Hughes, Michael A Mastrangelo, Jennifer L Tibbens, Howard J Federoff, William J Bowers

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Overview and Current Status of Alzheimer's Disease in Bangladesh.Journal of Alzheimer's disease reports · 2017
    Review
  6. Silibinin ameliorates AβNeurochemical research · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CNS expression of anti-inflammatory cytokine interleukin-4 attenuates Alzheimer's disease-like pathogenesis in APP+PS1 bigenic mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Immune-directed gene therapeutic development for Alzheimer's, prion, and Parkinson's diseases.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2009
    Review
  20. 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

6 authors at 1 institution in 1 country.

Maria E FrazerCenter for Aging and Developmental Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.
Jennifer E Hughes
Michael A Mastrangelo
Jennifer L Tibbens
Howard J Federoff
William J Bowers
University of Rochester · US

Funding

IMPROVED HSV VECTORS--GENE TRANSFER INTO NERVOUS SYSTEMR01NS036420 · NINDS · UNIVERSITY OF ROCHESTER · PI FEDEROFF, HOWARD J. · 1997 to 2005
$2.8M
Novel Mouse Model to Dissect Alzheimer's Disease PathophysiologyR01AG023593 · NIA · UNIVERSITY OF ROCHESTER · PI BOWERS, WILLIAM J. · 2004 to 2008
$1.3M
NIA NIH HHS R01 AG023593NIA NIH HHS R01-AG023593NINDS NIH HHS R01 NS036420NINDS NIH HHS R01-NS036420
6 · The paper itself

Abstract

Immunotherapeutics designed to dissolve existing amyloid plaques or to interrupt amyloid-beta (Abeta) accumulation may be feasible for treatment and/or prevention of Alzheimer's disease (AD). "Shaping" the immune responses elicited against Abeta is requisite toward generating an efficacious and safe outcome; this can be achieved by minimizing the possibility of deleterious inflammatory reactions in the brain as observed in clinical testing of Abeta peptide/adjuvant-based modalities. Herpes simplex virus (HSV)-based amplicons can coexpress multiple antigens and/or immunomodulatory genes due to their large genetic size capacity, thereby facilitating antigen-specific immune response shaping. We have constructed an amplicon (HSV(IE)Abeta(CMV)IL-4) that co-delivers Abeta(1-42) with interleukin-4 (IL-4), a cytokine that promotes the generation of Th2-like T-cell responses, which are favored in the setting of AD immunotherapy. Triple-transgenic AD (3xTg-AD) mice, which progressively develop both amyloid and neurofibrillary tangle pathology, were vaccinated thrice with HSV(IE)Abeta(CMV)IL-4, or a set of control amplicon vectors. Increased Th2-related, Abeta-specific antibodies, improved learning and functioning of memory, and prevention of AD-related amyloid and tau pathological progression were observed significantly more in the HSV(IE)Abeta(CMV)IL-4 vaccinated mice as compared to the other experimental groups. Our study underscores the potential of Abeta immunotherapy for AD and highlights the potency of amplicons in facilitating the immune response modulation to a disease-relevant antigen.

Indexed as

Gene Expression RegulationAlzheimer DiseaseAmyloid beta-PeptidesAnimalsBehavior, AnimalCricetinaeCytokinesGenetic TherapyImmunotherapyInterleukin-4LearningMemoryMiceMice, TransgenicNIH 3T3 CellsSimplexvirusAmyloid beta-PeptidesCytokinesInterleukin-4

Identifiers

PMID18388924
PMCPMC2441486
OpenAlexW2167838391

What OpenQuestion holds

Textmetadata
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.