Evidence map›Paper›PMID 34274825›Full record

ArticleJournal of autoimmunity2021

CD8 follicular T cells localize throughout the follicle during germinal center reactions and maintain cytolytic and helper properties.

Kristen M Valentine, Genevieve N Mullins, Oscar A Davalos, Lek Wei Seow, Katrina K Hoyer

Open access · greenAbstract read
In one paragraph

Article in Journal of autoimmunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Tissue-distinct Features of Follicular Cytotoxic CD8bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. The role of CD40L-expressing CXCR5Immunologic research · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. An angel or a devil? Current view on the role of CD8Journal of translational medicine · 2024
    Review
  10. CXCR5Frontiers in medicine · 2022
    Review
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

5 authors at 1 institution in 1 country.

Kristen M ValentineQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, CA, 95343, USA.
Genevieve N MullinsQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, CA, 95343, USA.
Oscar A DavalosQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, CA, 95343, USA.
Lek Wei SeowDepartment of Molecular and Cell Biology, School of Natural Sciences, University of California Merced, Merced, CA, 95343, USA.
Katrina K HoyerQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, CA, 95343, USA; Department of Molecular and Cell Biology, School of Natural Sciences, University of California Merced, Merced, CA, 95343, USA; Health Sciences Research Institute, University of California Merced, Merced, CA, 95343, USA. Electronic address: khoyer2@ucmerced.edu.
University of California, Merced · US

Funding

Cytokine Dysregulation in Autoimmune Hemolytic AnemiaR00HL090706 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI HOYER, KATRINA K · 2012 to 2014
$716k
Experimental and mathematical modeling of CD8 T cell dynamics in autoimmune diseaseR15HL146779 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI HOYER, KATRINA K · 2018 to 2020
$554k
NHLBI NIH HHS R00 HL090706NHLBI NIH HHS R15 HL146779
6 · The paper itself

Abstract

Follicular CXCR5+ PD-1+ CD8 T cells (CD8 Tfc) arise in multiple models of systemic autoimmunity yet their functional contribution to disease remains in debate. Here we define the follicular localization and functional interactions of CD8 Tfc with B cells during autoimmune disease. The absence of functional T regulatory cells in autoimmunity allows for CD8 Tfc development that then expands with lymphoproliferation. CD8 Tfc are identifiable within the lymph nodes and spleen during systemic autoimmunity, but not during tissue-restricted autoimmune disease. Autoimmune CD8 Tfc cells are polyfunctional, producing helper cytokines IL-21, IL-4, and IFNγ while maintaining cytolytic proteins CD107a, granzyme B, and TNF. During autoimmune disease, IL-2-KO CD8 T cells infiltrate the B cell follicle and germinal center, including the dark zone, and in vitro induce activation-induced cytidine deaminase in naïve B cells via IL-4 secretion. CD8 Tfc represent a unique CD8 T cell population with a diverse effector cytokine repertoire that can contribute to pathogenic autoimmune B cell response.

Indexed as

Cytotoxicity, ImmunologicAICDA (Activation-Induced Cytidine Deaminase)AnimalsAutoimmune DiseasesB-LymphocytesCD8-Positive T-LymphocytesCytidine DeaminaseCytokine-Induced Killer CellsFemaleGerminal CenterMaleMiceMice, Inbred BALB CT Follicular Helper CellsAICDA (Activation-Induced Cytidine Deaminase)Cytidine DeaminaseAutoimmunityCD8 T follicular CellsCXCR5+ CD8 T cellGerminal centerT regulatory cell

Identifiers

PMID34274825
PMCPMC9374523
OpenAlexW3183436358

What OpenQuestion holds

Textmetadata
LicenceTDM
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.