Evidence map›Paper›PMID 24493798›Full record

ArticleThe Journal of experimental medicine2014

Antiviral drug ganciclovir is a potent inhibitor of microglial proliferation and neuroinflammation.

Zhaoqing Ding, Vidhu Mathur, Peggy P Ho, Michelle L James, Kurt M Lucin, Aileen Hoehne, Haitham Alabsi, Sanjiv S Gambhir, Lawrence Steinman, Jian Luo and 1 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06436534 (A Randomized, Double-blind, Placebo-controlled, Single-center Clinical Trial of Ganciclovir Capsules in the Treatment of Refractory Moderate-to-severe Allergic Rhinitis), which is not on this map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 4% 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.

NCT06436534 narecruitingnot on this mapstarted 2024, after this paper: background citation

A Randomized, Double-blind, Placebo-controlled, Single-center Clinical Trial of Ganciclovir Capsules in the Treatment of Refractory Moderate-to-severe Allergic Rhinitis

TypeinterventionalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2024 to 2026Enrolled50ConditionsRhinitis, AllergicArmsGanciclovir Oral Capsule, Ganciclovir Simulant Oral Capsule, Mometasone Nasal
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Zhaoqing DingStanford, Department of Radiology; Stanford University School of Medicine, Stanford, CA 94305.
Vidhu Mathur
Peggy P Ho
Michelle L James
Kurt M Lucin
Aileen Hoehne
Haitham Alabsi
Sanjiv S Gambhir
Lawrence Steinman
Jian Luo
Tony Wyss-Coray
Stanford University · USVA Palo Alto Health Care System · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
TGFbeta signaling in neurodegeneration and Alzhimer'sR01AG027505 · NIA · STANFORD UNIVERSITY · PI WYSS-CORAY, TONY · 2006 to 2010
$1.3M
Role of Microglia Proliferation in Experimental Autoimmune EncephalomyelitisF31NS066676 · NINDS · STANFORD UNIVERSITY · PI DING, ZHAOQING · 2010 to 2011
$64k
NIAID NIH HHS T32 AI007290NIAID NIH HHS T32 AI07290NIA NIH HHS R01 AG027505NIA NIH HHS R01AG27505NINDS NIH HHS F31 NS066676
6 · The paper itself

Abstract

Aberrant microglial responses contribute to neuroinflammation in many neurodegenerative diseases, but no current therapies target pathogenic microglia. We discovered unexpectedly that the antiviral drug ganciclovir (GCV) inhibits the proliferation of microglia in experimental autoimmune encephalomyelitis (EAE), a mouse model for multiple sclerosis (MS), as well as in kainic acid-induced excitotoxicity. In EAE, GCV largely prevented infiltration of T lymphocytes into the central nervous system (CNS) and drastically reduced disease incidence and severity when delivered before the onset of disease. In contrast, GCV treatment had minimal effects on peripheral leukocyte distribution in EAE and did not inhibit generation of antibodies after immunization with ovalbumin. Additionally, a radiolabeled analogue of penciclovir, [(18)F]FHBG, which is similar in structure to GCV, was retained in areas of CNS inflammation in EAE, but not in naive control mice, consistent with the observed therapeutic effects. Our experiments suggest GCV may have beneficial effects in the CNS beyond its antiviral properties.

Indexed as

AnimalsAntiviral AgentsBrainCD4-Positive T-LymphocytesCell ProliferationEncephalomyelitis, Autoimmune, ExperimentalGanciclovirImmunosuppressive AgentsMiceMice, Inbred C57BLMicrogliaOvalbuminT-Lymphocyte SubsetsAntiviral AgentsGanciclovirImmunosuppressive AgentsOvalbumin

Identifiers

PMID24493798
PMCPMC3920559
OpenAlexW2116414892

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.