Evidence map›Paper›PMID 41993267›Full record

ArticlebioRxiv : the preprint server for biology2026

Viral Microglia Reprogramming Clears Oligomeric Neurotoxic Debris.

Griffin P Carter, Zachary P McKay, Mark A Katz, Lisbeth Disla, Dasean T Nardone-White, Derek Southwell, Michael C Brown, Matthias Gromeier

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Griffin P CarterDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0003-0448-3989
Zachary P McKayDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0002-9198-9891
Mark A KatzDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0009-0001-2438-4542
Lisbeth DislaDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0009-0004-9220-4293
Dasean T Nardone-WhiteDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0001-9523-3445
Derek SouthwellDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0001-6465-3869
Michael C BrownDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0002-3957-1164
Matthias GromeierDepartment of Molecular Genetics & Microbiology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0003-4538-0302

Funding

Innate Antiviral Signals for Cancer ImmunotherapyR01NS108773 · NINDS · DUKE UNIVERSITY · PI Matthias Gromeier, Smita K. Nair · 2018 to 2026
$3.3M
Resolving Spatiotemporal Dynamics of Recombinant Poliovirus ImmunotherapyR01CA281320 · NCI · DUKE UNIVERSITY · PI Matthias Gromeier · 2023 to 2026
$1.7M
Reviving cancer immune surveillance with CD4 T cell helpR00CA263021 · NCI · DUKE UNIVERSITY · PI BROWN, MICHAEL CLAVON · 2022 to 2024
$737k
Leica Stellaris Confocal for a Campus-wide Shared ResourceS10OD034340 · OD · DUKE UNIVERSITY · PI CAMERON, LISA A. · 2024 to 2024
$686k
NCI NIH HHS R00 CA263021NCI NIH HHS R01 CA281320NIH HHS S10 OD034340NINDS NIH HHS R01 NS108773
6 · The paper itself

Abstract

Owing to pivotal roles in CNS debris clearance and homeostasis, microglia are central targets for the therapy of neurodegenerative diseases. Intricate proximity to neurons, the inherent danger of neuroimmune toxicity, and intrinsically high plasticity and adaptability, impose high hurdles on microglia modulation. Attenuated viruses are being tested extensively against CNS malignancies (i.e., cancer virotherapy); yet, aside from viral vector-mediated payload delivery, virotherapy for non-neoplastic CNS disease remains unexplored. Here we report disseminated targeting of microglia with the highly attenuated polio:rhinovirus chimera, PVSRIPO, that culminated in profound, durable microglia reprogramming. This phenotype, rooted in extended cytoplasmic viral (v)RNA replication, was non-cytopathogenic and did not yield virus progeny or dissemination. vRNA replication in microglia triggered selective interferon (IFN) regulatory factor (IRF) 3/IRF7 transcriptional programs in the relative absence of NFκB-driven proinflammatory cytokine responses and elicited robust phagocytosis of both tumor cells and amyloid-beta. Targeting of microglia with PVSRIPO mediated immunotherapy in a mouse glioma model and the clearance of oligomeric amyloid-beta deposits in an injectable model of neurotoxic amyloid accumulation. This work identifies attenuated virotherapy as an approach to safely and effectively invigorate microglia function in immune surveillance and neurotoxic debris clearance.

Identifiers

PMID41993267
PMCPMC13082030

What OpenQuestion holds

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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.