Evidence map›Paper›PMID 41918222›Full record

ArticleImmunology and cell biology2026

IL-1β and IL-6 synergistically drive murine TFH cell differentiation and maintenance in vitro.

Juliana Restrepo Munera, S Rameeza Allie

Abstract read
In one paragraph

Article in Immunology and cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Juliana Restrepo MuneraDepartment of Cell and Biological Systems, Penn State College of Medicine, Hershey, PA, USA.
S Rameeza AllieDepartment of Cell and Biological Systems, Penn State College of Medicine, Hershey, PA, USA.ORCID https://orcid.org/0000-0001-8877-1931

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T follicular helper (TFH) cells are critical in supporting B-cell responses, which ultimately establish long-term protective immunity against infection and some cancers by producing protective B cells, including antibody-secreting cells and memory cells. However, this same GC output can also promote autoimmune pathology. Therefore, TFH cells are at the core of humoral immunity, underscoring TFH cells as targets for long-term protective and/or pathologic immune responses. Here we define conditions that promote physiologically relevant TFH cell differentiation in vitro. We demonstrate that in addition to T-cell receptor (TCR) signaling, IL-6 and IL-1β individually and jointly promote TFH cell differentiation. These findings highlight key requirements for generating functional TFH cells, providing a model to study therapeutic impacts on TFH cells across diverse disease settings.

Indexed as

Cell DifferentiationInterleukin-1betaInterleukin-6T Follicular Helper CellsAnimalsB-LymphocytesMiceMice, Inbred C57BLReceptors, Antigen, T-CellSignal TransductionInterleukin-1betaInterleukin-6Receptors, Antigen, T-CellCytokinesDifferentiationIL‐1βIL‐6In vitroTFH cell

Identifiers

PMID41918222
PMCPMC13155040

What OpenQuestion 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 OpenQuestion graph.