Evidence map›Paper›PMID 36282595›Full record

ArticleJCI insight2022

IL-6-targeted therapies to block the cytokine or its receptor drive distinct alterations in T cell function.

Cate Speake, Tania Habib, Katharina Lambert, Christian Hundhausen, Sandra Lord, Matthew J Dufort, Samuel O Skinner, Alex Hu, MacKenzie Kinsman, Britta E Jones and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Review
  3. Selected Cannabinoids, Cannabimimetic Agents andPharmaceuticals (Basel, Switzerland) · 2026
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  5. Memory CD4Frontiers in immunology · 2026
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  9. Article
  10. Current status of pancreatic islet xenotransplantation.Clinical transplantation and research · 2025
    Review
  11. Article
  12. Review
  13. Article
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  15. 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

16 authors at 2 institutions in 2 countries.

Cate SpeakeCenter for Interventional Immunology.
Tania HabibCenter for Translational Immunology.
Katharina LambertCenter for Translational Immunology.
Christian HundhausenCenter for Translational Immunology.
Sandra LordCenter for Interventional Immunology.
Matthew J DufortCenter for Systems Immunology, and.
Samuel O SkinnerCenter for Interventional Immunology.
Alex HuCenter for Systems Immunology, and.
MacKenzie KinsmanCenter for Translational Immunology.
Britta E JonesCenter for Translational Immunology.
Megan D MaerzCenter for Translational Immunology.
Megan TatumCenter for Translational Immunology.
Anne M HockingCenter for Translational Immunology.
Gerald T NepomImmune Tolerance Network, Benaroya Research Institute at Virginia Mason, Seattle, Washington, USA.
Carla J GreenbaumCenter for Interventional Immunology.
Jane H BucknerCenter for Translational Immunology.
Center for Translational Molecular Medicine · NLImmune Tolerance Network · US

Funding

Mechanisms of IL-6 mediated T cell pathogenesis in autoimmunityR01AI132774 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI ALTMAN, MATTHEW C., BUCKNER, JANE HOYT · 2017 to 2020
$6.4M
NIAID NIH HHS R01 AI132774
6 · The paper itself

Abstract

Therapeutics that inhibit IL-6 at different points in its signaling pathway are in clinical use, yet whether the immunological effects of these interventions differ based on their molecular target is unknown. We performed short-term interventions in individuals with type 1 diabetes using anti-IL-6 (siltuximab) or anti-IL-6 receptor (IL-6R; tocilizumab) therapies and investigated the impact of this in vivo blockade on T cell fate and function. Immune outcomes were influenced by the target of the therapeutic intervention (IL-6 versus IL-6R) and by peak drug concentration. Tocilizumab reduced ICOS expression on T follicular helper cell populations and T cell receptor-driven (TCR-driven) STAT3 phosphorylation. Siltuximab reversed resistance to Treg-mediated suppression and increased TCR-driven phosphorylated STAT3 and production of IL-10, IL-21, and IL-27 by T effectors. Together, these findings indicate that the context of IL-6 blockade in vivo drives distinct T cell-intrinsic changes that may influence therapeutic outcomes.

Indexed as

CytokinesReceptors, Antigen, T-CellHumansPhosphorylationSignal TransductionCytokinesReceptors, Antigen, T-CellAutoimmunityCytokinesImmunologyImmunotherapyT cells

Identifiers

PMID36282595
PMCPMC9746808
OpenAlexW4307210278

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.