Evidence map›Paper›PMID 20205645›Full record

ReviewCNS & neurological disorders drug targets2010

Impact of the CD40-CD40L dyad in Alzheimer's disease.

Brian Giunta, Kavon Rezai-Zadeh, Jun Tan

Open access · greenAbstract readReview
In one paragraph

Review in CNS & neurological disorders drug targets, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. CD40-CD40L in Neurological Disease.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Regulatory role of cytosolic phospholipase AJournal of neuroinflammation · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Inflammation, immunity, and Alzheimer's disease.CNS & neurological disorders drug targets · 2010
    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

3 authors at 1 institution in 1 country.

Brian GiuntaDepartment of Psychiatry & Behavioral Medicine, Institute for Research in Psychiatry Neuroimmunology Laboratory, University of South Florida College of Medicine, Tampa, FL 33613, USA. bgiunta@health.usf.edu
Kavon Rezai-Zadeh
Jun Tan
University of South Florida · US

Funding

The Role of HIV-1 Tat in Alzheimer's DiseaseK08MH082642 · NIMH · UNIVERSITY OF SOUTH FLORIDA · PI GIUNTA, BRIAN · 2008 to 2011
$576k
Oral administration of TeaMemTM inhibits Alzheimer's disease pathogenesisR43AT004871 · NCCIH · NATURA THERAPEUTICS, INC. · PI SANBERG, CYNDY DAVIS, TAN, JUN · 2008 to 2009
$179k
DiosMemTM, a natural gamma-secretase inhibitor, opposes AD pathogenesisR43AG033417 · NIA · NATURA THERAPEUTICS, INC. · PI SANBERG, CYNDY DAVIS, TAN, JUN · 2009 to 2009
$165k
HUCBC modulation of Alzheimer-like pathology and behavioral changesR41AG031586 · NIA · SANERON CCEL THERAPEUTICS, INC. · PI TAN, JUN · 2007 to 2007
$140k
NCCIH NIH HHS 1R43AT004871-01NCCIH NIH HHS R43 AT004871NIA NIH HHS 1R41AG031586-01NIA NIH HHS 1R43AG033417-01NIA NIH HHS R41 AG031586NIA NIH HHS R43 AG033417NIMH NIH HHS 1 K08 MH082642-01A1NIMH NIH HHS K08 MH082642
6 · The paper itself

Abstract

As the number of elderly individuals rises, Alzheimer's disease (AD), marked by amyloid-beta deposition, neurofibrillary tangle formation, and low-level neuroinflammation, is expected to lead to an ever-worsening socioeconomic burden. AD pathoetiologic mechanisms are believed to involve chronic microglial activation. This phenomenon is associated with increased expression of membrane-bound CD40 with its cognate ligand, CD40 ligand (CD40L), as well as increased circulating levels of soluble forms of CD40 (sCD40) and CD40L (sCD40L). Here, we review the role of this inflammatory dyad in the pathogenesis of AD. In addition, we examine potential therapeutic strategies such as statins, flavonoids, and human umbilical cord blood transplantation, all of which have been shown to modulate CD40-CD40L interaction in mouse models of AD. Importantly, therapeutic approaches focusing on CD40-CD40L dyad regulation, either alone or in combination with amyloid-beta immunotherapy, may provide for a safe and effective AD prophylaxis or treatment in the near future.

Indexed as

Alzheimer DiseaseAlzheimer VaccinesAmyloid beta-PeptidesAnimalsCD40 AntigensCD40 LigandCord Blood Stem Cell TransplantationEncephalitisFlavonoidsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMiceModels, NeurologicalAlzheimer VaccinesAmyloid beta-PeptidesCD40 AntigensCD40 LigandFlavonoidsHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID20205645
PMCPMC2892111
OpenAlexW2115366527

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.