Evidence map›Paper›PMID 41499853›Full record

ArticleVeterinary microbiology2026

Beyond macrophages: FIPV tropism includes T and B lymphocytes.

Aadhavan Balakumar, Patrawin Wanakumjorn, Kazuto Kimura, Ehren McLarty, Katherine Farrell, Terza Brostoff, Jully Pires, Tamar Cohen-Davidyan, Jennifer M Cassano, Brian Murphy and 2 more

Abstract read
In one paragraph

Article in Veterinary microbiology, 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. 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

12 authors.

Aadhavan BalakumarPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Patrawin WanakumjornPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Kazuto KimuraPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Ehren McLartyVeterinary Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA, USA.
Katherine FarrellVeterinary Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA, USA.
Terza BrostoffPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Jully PiresThe Veterinary Center for Clinical Trials, School of Veterinary Medicine, University of California, Davis, CA, USA.
Tamar Cohen-DavidyanThe Veterinary Center for Clinical Trials, School of Veterinary Medicine, University of California, Davis, CA, USA.
Jennifer M CassanoThe Regenerative Medicine Laboratory, Veterinary Institute for Regenerative Cures, School of Veterinary Medicine, University of California, Davis, CA, USA.
Brian MurphyPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Krystle ReaganVeterinary Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA, USA.
Amir KolPathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, CA, USA. Electronic address: akol@ucdavis.edu.

Funding

Multi-pronged therapy for immune system regeneration and recovery in a FIP model of MIS-CR21HD106027 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KOL, AMIR · 2021 to 2022
$432k
NICHD NIH HHS R21 HD106027
6 · The paper itself

Abstract

If untreated, feline infectious peritonitis (FIP) is a fatal disease that is caused by feline infectious peritonitis virus (FIPV), a virulent biotype of feline coronavirus (FCoV) that disseminates broadly and triggers severe systemic inflammation. While the prevailing model holds that FIPV selectively infects monocytes/macrophages, the full range of susceptible cell types and the mechanisms of immune cell invasion remain poorly defined. Here, we applied single-cell RNA sequencing, multiplex immunofluorescence, and in situ hybridization to mesenteric lymph node aspirates and formalin fixed and paraffin embedded lymph node tissues from cats with naturally occurring effusive FIP. We identified FIPV RNA and nucleocapsid protein in T and B lymphocytes and myeloid cells, and subgenomic viral RNA in T cells, demonstrating cell entry and viral genomic replication across multiple immune compartments. Rare FIPV RNA-positive lymphocytes persisted after antiviral treatment cessation and resolution of clinical signs. These findings revise current models of FIPV pathogenesis and reveal new insights into coronavirus-driven immune dysregulation, viral persistence, and relapse. Our study highlights the utility of FIP as a naturally occurring animal model for exploring adaptive immune cell infection in coronavirus diseases, providing a translational platform for understanding virus-host interactions that drive chronic or relapsing immunopathology.

Indexed as

B-LymphocytesCoronavirus, FelineFeline Infectious PeritonitisMacrophagesT-LymphocytesViral TropismAnimalsCatsLymph NodesRNA, ViralRNA, ViralFeline infectious peritonitis virusLymphocyte infectionViral tropism

Identifiers

PMID41499853
PMCPMC13088912

What OpenQuestion holds

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LicenceCC BY
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.