Evidence map›Paper›PMID 30372487›Full record

ArticlePLoS pathogens2018

CD4 T cells control development and maintenance of brain-resident CD8 T cells during polyomavirus infection.

Taryn E Mockus, Shwetank, Matthew D Lauver, Heather M Ren, Colleen S Netherby, Tarik Salameh, Yuka Imamura Kawasawa, Feng Yue, James R Broach, Aron E Lukacher

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 14% 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.

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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Evolving role of CD8Frontiers in immunology · 2026
    Review
  3. Observational
  4. Unraveling the complexities of neurotropic virus infection and immune evasion.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  5. Review
  6. Article
  7. Protective function and differentiation cues of brain-resident CD8+ T cells during surveillance of latentProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Article
  10. Tissue-resident immune cells in the pathogenesis of multiple sclerosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  11. Review
  12. Review
  13. Review
  14. Memory CD8Immunology · 2021
    Article
  15. High anti-JCPyV serum titers coincide with high CSF cell counts in RRMS patients.Multiple sclerosis (Houndmills, Basingstoke, England) · 2021
    Article
  16. Interleukin-21 in Viral Infections.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Review
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Taryn E MockusDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.
ShwetankDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0002-5069-603X
Matthew D LauverDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0002-7001-9730
Heather M RenDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.
Colleen S NetherbyDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0001-5676-768X
Tarik SalamehDepartment of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0002-2344-4670
Yuka Imamura KawasawaDepartment of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0002-8638-6738
Feng YueDepartment of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA, United States of America.
James R BroachDepartment of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0003-1197-0312
Aron E LukacherDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, United States of America.ORCID 0000-0002-7969-2841
Penn State Milton S. Hershey Medical Center · USPennsylvania State University · US

Funding

Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
NRSA Training CoreTL1TR002016 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI THOMAS, GAIL D. · 2016 to 2025
$3.4M
A Mouse Model to Define Immunovirologic Determinants of Polyomavirus CNS DiseaseR01NS088367 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LUKACHER, ARON ELIOT · 2014 to 2021
$2.8M
Pathogenesis of Mouse Polyomavirus-associated CNS DemyelinationR01NS092662 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LUKACHER, ARON ELIOT · 2016 to 2022
$2.1M
Generation of CNS-resident memory T cells and mechanisms of glial cell dysfunction during polyomavirus encephalitisF32NS106730 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI NETHERBY-WINSLOW, COLLEEN S · 2018 to 2020
$136k
NCATS NIH HHS TL1 TR002016NCATS NIH HHS UL1 TR002014NINDS NIH HHS F32 NS106730NINDS NIH HHS R01 NS088367NINDS NIH HHS R01 NS092662
6 · The paper itself

Abstract

Tissue-resident memory CD8 T (TRM) cells defend against microbial reinfections at mucosal barriers; determinants driving durable TRM cell responses in non-mucosal tissues, which often harbor opportunistic persistent pathogens, are unknown. JC polyomavirus (JCPyV) is a ubiquitous constituent of the human virome. With altered immunological status, JCPyV can cause the oft-fatal brain demyelinating disease progressive multifocal leukoencephalopathy (PML). JCPyV is a human-only pathogen. Using the mouse polyomavirus (MuPyV) encephalitis model, we demonstrate that CD4 T cells regulate development of functional antiviral brain-resident CD8 T cells (bTRM) and renders their maintenance refractory to systemic CD8 T cell depletion. Acquired CD4 T cell deficiency, modeled by delaying systemic CD4 T cell depletion until MuPyV-specific CD8 T cells have infiltrated the brain, impacted the stability of CD8 bTRM, impaired their effector response to reinfection, and rendered their maintenance dependent on circulating CD8 T cells. This dependence of CD8 bTRM differentiation on CD4 T cells was found to extend to encephalitis caused by vesicular stomatitis virus. Together, these findings reveal an intimate association between CD4 T cells and homeostasis of functional bTRM to CNS viral infection.

Indexed as

AnimalsBrainCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationFemaleImmunologic MemoryLymphocyte DepletionMaleMiceMice, Inbred C57BLPolyomavirusPolyomavirus Infections

Identifiers

PMID30372487
PMCPMC6224182
OpenAlexW2899192123

What Socratic holds

Textmetadata
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 Socratic graph.