Evidence map›Paper›PMID 31085590›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Widespread Tau-Specific CD4 T Cell Reactivity in the General Population.

Cecilia S Lindestam Arlehamn, John Pham, Roy N Alcalay, April Frazier, Evan Shorr, Chelsea Carpenter, John Sidney, Rekha Dhanwani, Julian Agin-Liebes, Francesca Garretti and 7 more

Registry-linked trialOpen access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04239079 (Autoimmune Features of Neurodegenerative Disorders), which is not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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.

NCT04239079 recruitingnot on this map

Autoimmune Features of Neurodegenerative Disorders

TypeobservationalSponsorColumbia UniversityRan2019 to 2028Enrolled120ConditionsParkinson Disease, Alzheimer Disease, Mild Cognitive Impairment
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. CD4Cells · 2024
    Review
  8. PINK1 is a target of T cell responses in Parkinson's disease.bioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. T cell aging and Alzheimer's disease.Frontiers in immunology · 2023
    Review
  11. Article
  12. CD11bJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  13. Article
  14. Review
  15. T cells, α-synuclein and Parkinson disease.Handbook of clinical neurology · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Inflammation in Experimental Models of α-Synucleinopathies.Movement disorders : official journal of the Movement Disorder Society · 2021
    Review
  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

17 authors at 4 institutions in 2 countries.

Cecilia S Lindestam ArlehamnDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.ORCID 0000-0001-7302-8002
John PhamDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.
Roy N AlcalayDepartment of Neurology, Columbia University Irving Medical Center, New York State Psychiatric Institute, New York, NY 10032.
April FrazierDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.
Evan ShorrDepartment of Psychiatry, Columbia University Irving Medical Center, New York State Psychiatric Institute, New York, NY 10032.ORCID 0000-0003-4521-3993
Chelsea CarpenterDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.
John SidneyDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.ORCID 0000-0002-0987-405X
Rekha DhanwaniDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.ORCID 0000-0002-6592-8657
Julian Agin-LiebesDepartment of Psychiatry, Columbia University Irving Medical Center, New York State Psychiatric Institute, New York, NY 10032.
Francesca GarrettiDepartment of Psychiatry, Columbia University Irving Medical Center, New York State Psychiatric Institute, New York, NY 10032.ORCID 0000-0002-6609-8034
Amy W AmaraDepartment of Neurology, University of Alabama at Birmingham, Birmingham, AL 35233.ORCID 0000-0003-0762-9656
David G StandaertDepartment of Neurology, University of Alabama at Birmingham, Birmingham, AL 35233.ORCID 0000-0003-2921-8348
Elizabeth J PhillipsVanderbilt University School of Medicine, Nashville, TN 37235.
Simon A MallalVanderbilt University School of Medicine, Nashville, TN 37235.ORCID 0000-0002-7036-1309
Bjoern PetersDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.ORCID 0000-0002-8457-6693
David SulzerDepartment of Neurology, Columbia University Irving Medical Center, New York State Psychiatric Institute, New York, NY 10032.
Alessandro SetteDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037; alex@lji.org.ORCID 0000-0001-7013-2250
La Jolla Institute for Immunology · USColumbia University Irving Medical Center · USMurdoch University · AUUniversity of Alabama at Birmingham · US

Funding

Project 3: LRRK2 mediated macrophage responses in PDP50NS108675 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STANDAERT, DAVID G. · 2018 to 2022
$9.9M
Autoimmune Features of Neurodegenerative DisordersR01NS095435 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SETTE, ALESSANDRO, SULZER, DAVID · 2018 to 2022
$4.2M
NINDS NIH HHS P50 NS108675NINDS NIH HHS R01 NS095435
6 · The paper itself

Abstract

Tau protein is found to be aggregated and hyperphosphorylated (p-tau) in many neurologic disorders, including Parkinson disease (PD) and related parkinsonisms, Alzheimer disease, traumatic brain injury, and even in normal aging. Although not known to produce autoimmune responses, we hypothesized that the appearance of aggregated tau and p-tau with disease could activate the immune system. We thus compared T cell responses to tau and p-tau-derived peptides between PD patients, age-matched healthy controls, and young healthy controls (<35 y old; who are less likely to have high levels of tau aggregates). All groups exhibited CD4

Indexed as

AdultAgedAged, 80 and overAutoimmunityCD4-Positive T-LymphocytesCells, CulturedClonal Selection, Antigen-MediatedFemaleHumansImmune ToleranceMaleMiddle AgedPeptidesPhosphorylationProtein Aggregation, Pathologicaltau ProteinsPeptidestau Proteins

Identifiers

PMID31085590
PMCPMC6581570
OpenAlexW2945307828

What OpenQuestion holds

Textmetadata
LicenceTDM
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.