Evidence map›Paper›PMID 41772634›Full record

ArticleJournal of neuroinflammation2026

Interferon-induced protein IFIT3 as a molecular nexus of neuroinflammation in Alzheimer's disease and HIV-associated neurocognitive disorders.

Ranjit Kumar Das, Nirakar Sahoo, Deepa Roy, Lauren Nguyen, Hansapani Rodrigo, Asim K Duttaroy, Jerel Adam Fields, Upal Roy

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Increased Amyloidogenic Neuronal Injury in HIV-1-infected APP-KI Alzheimer's disease mice.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. 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

8 authors.

Ranjit Kumar DasDepartment of Health and Biomedical Sciences, University of Texas Rio Grande Valley, One West University Blvd, Brownsville, Texas, 78520, USA.
Nirakar SahooSchool of Integrative Biological and Chemical Sciences, University of Texas Rio Grande Valley, Edinburg, Texas, USA.
Deepa RoyDepartment of Health and Biomedical Sciences, University of Texas Rio Grande Valley, One West University Blvd, Brownsville, Texas, 78520, USA.
Lauren NguyenDepartment of Psychiatry, University of California School of Medicine, San Diego, CA, USA.
Hansapani RodrigoSchool of Mathematical and Statistical Sciences, University of Texas Rio Grande Valley, Edinburg, TX, USA.
Asim K DuttaroyDepartment of Nutrition, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway.
Jerel Adam FieldsDepartment of Psychiatry, University of California School of Medicine, San Diego, CA, USA.
Upal RoyDepartment of Health and Biomedical Sciences, University of Texas Rio Grande Valley, One West University Blvd, Brownsville, Texas, 78520, USA. upal.roy@utrgv.edu.

Funding

NASA-MUREP, NASA-MOSAIC, UTRGV-Resource Centers for Minority Aging Research (RCMAR) P30AG059305National Institute of Health, USA R15NS108815 and R01AI147731NIMHD grant U54MD019970UTRGV internal funding SC2GM139715
6 · The paper itself

Abstract

Alzheimer’s disease (AD) and HIV-associated neurocognitive disorder (HAND) are significant global health concerns characterized by cognitive impairment and shared pathological features, including chronic neuroinflammation, amyloid deposition, and immune dysregulation. However, the precise molecular connections between these disorders remain unclear. Here, we identify IFIT3 as a critical shared mediator of neuroinflammatory responses in both AD and HAND. Using complementary approaches, including neuronal and microglial cell cultures, the APP/PS1 mouse model, and human postmortem brain tissues, we demonstrate consistent IFIT3 upregulation in response to amyloid-beta (Aβ) and HIV-1 exposure, with notably enhanced expression under combined conditions. Treatment with combination antiretroviral therapy (cART) partially mitigated IFIT3 induction. Additionally, siRNA-mediated silencing of IFIT3 significantly reduced key inflammatory mediators, including mitochondrial antiviral signaling protein (MAVS), nuclear factor-κB, and proinflammatory cytokines. Clinically, elevated IFIT3 expression was associated with early HAND and progressively increased across advancing AD Braak stages. Together, these findings identify IFIT3 as a potential molecular bridge between HAND and AD, highlighting its promise as both a biomarker and a therapeutic target for inflammation-driven neurodegeneration.

Indexed as

AIDS Dementia ComplexAlzheimer DiseaseNeuroinflammatory DiseasesAmyloid beta-PeptidesAnimalsBrainCells, CulturedFemaleHumansIntracellular Signaling Peptides and ProteinsMaleMiceMice, TransgenicMicrogliaRNA-Binding ProteinsAmyloid beta-PeptidesIFIT3 protein, humanIntracellular Signaling Peptides and ProteinsRNA-Binding ProteinsAgingAlzheimer’s diseaseBiomarkerHANDIFIT3Neuroinflammation

Identifiers

PMID41772634
PMCPMC13059446

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.