Evidence map›Paper›PMID 25667322›Full record

ArticleThe Journal of general virology2015

Anti-inflammatory activity of intravenous immunoglobulins protects against West Nile virus encephalitis.

Ruchi Srivastava, Chandran Ramakrishna, Edouard Cantin

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06590207 (Administering Convalescent Plasma Rich With Neutralizing Abs. to Hospitalized Adults With WNV - a Double-blind Randomized Controlled Study), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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.

NCT06590207 phase3completednot on this mapstarted 2024, after this paper: background citation

Administering Convalescent Plasma Rich With Neutralizing Abs. to Hospitalized Adults With WNV - a Double-blind Randomized Controlled Study

TypeinterventionalSponsorSheba Medical CenterRan2024 to 2025Enrolled200ConditionsWest Nile Fever With Neurologic Manifestation (Diagnosis), West Nile Fever Without ComplicationsArmsplasma rich with WNV neutralizing antibodies, Saline
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  10. Risk Factors of Neurological Complications in Severe Fever Patients with Thrombolytic Syndrome: A Single-Center Retrospective Study in China.Medical science monitor : international medical journal of experimental and clinical research · 2021
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  11. Article
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  16. Intravenous Immunoglobulin Therapy EliminatesInternational journal of molecular sciences · 2019
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  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

3 authors at 2 institutions in 1 country.

Ruchi SrivastavaDepartment of Virology, Beckman Research Institute of City of Hope, Duarte, CA 91010-3000, USA.
Chandran RamakrishnaDepartment of Virology, Beckman Research Institute of City of Hope, Duarte, CA 91010-3000, USA.
Edouard CantinDepartment of Virology, Beckman Research Institute of City of Hope, Duarte, CA 91010-3000, USA.
Beckman Research InstituteCity of Hope · US

Funding

PHS HHS U54 A1065359
6 · The paper itself

Abstract

West Nile virus (WNV), an important global human pathogen, targets neurons to cause lethal encephalitis, primarily in elderly and immunocompromised patients. Currently, there are no approved therapeutic agents or vaccines to treat WNV encephalitis. Recent studies have suggested that inflammation is a major contributor to WNV encephalitis morbidity. In this study we evaluated the use of IVIG (intravenous immunoglobulins - a clinical product comprising pooled human IgG) as an anti-inflammatory treatment in a model of lethal WNV infection. We report here that IVIG and pooled human WNV convalescent sera (WNV-IVIG) inhibited development of lethal WNV encephalitis by suppressing central nervous system (CNS) infiltration by CD45(high) leukocytes. Pathogenic Ly6C(high) CD11b(+) monocytes were the major infiltrating subset in the CNS of infected control mice, whereas IVIG profoundly reduced infiltration of these pathogenic Ly6C(high) monocytes into the CNS of infected mice. Interestingly, WNV-IVIG was more efficacious than IVIG in controlling CNS inflammation when mice were challenged with a high-dose inoculum (10(5) versus 10(4) p.f.u.) of WNV. Importantly, adsorption of WNV E-glycoprotein neutralizing antibodies did not abrogate IVIG protection, consistent with virus neutralization not being essential for IVIG protection. These findings confirmed the potent immunomodulatory activity of generic IVIG, and emphasized its potential as an effective immunotherapeutic drug for encephalitis and other virus induced inflammatory diseases.

Indexed as

AnimalsAntibodies, ViralBrainDisease Models, AnimalHumansImmunoglobulins, IntravenousMice, Inbred BALB CMice, KnockoutMonocytesSurvival AnalysisTreatment OutcomeWest Nile FeverWest Nile virusAntibodies, ViralImmunoglobulins, Intravenous

Identifiers

PMID25667322
PMCPMC4635485
OpenAlexW1683506383

What OpenQuestion holds

Textmetadata
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.