Evidence map›Paper›PMID 38530780›Full record

ArticleRheumatology (Oxford, England)2024

Effects of interleukin-6 signal inhibition on Treg subpopulations and association of Tregs with clinical outcomes in rheumatoid arthritis.

Hiroto Yoshida, Mayu Magi, Hiroya Tamai, Jun Kikuchi, Keiko Yoshimoto, Kotaro Otomo, Yoshihiro Matsumoto, Mariko Noguchi-Sasaki, Tsutomu Takeuchi, Yuko Kaneko

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Elevated ST2Arthritis research & therapy · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Tocilizumab for Non-Infectious Uveitis: A Systematic Review.Journal of inflammation research · 2025
    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

10 authors at 1 institution in 1 country.

Hiroto YoshidaProduct Research Department, Chugai Pharmaceutical Co. Ltd, Kanagawa, Japan.ORCID 0009-0001-5111-0125
Mayu MagiProduct Research Department, Chugai Pharmaceutical Co. Ltd, Kanagawa, Japan.
Hiroya TamaiDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0001-8784-2224
Jun KikuchiDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Keiko YoshimotoDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Kotaro OtomoDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Yoshihiro MatsumotoProduct Research Department, Chugai Pharmaceutical Co. Ltd, Kanagawa, Japan.
Mariko Noguchi-SasakiProduct Research Department, Chugai Pharmaceutical Co. Ltd, Kanagawa, Japan.
Tsutomu TakeuchiDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Yuko KanekoDivision of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Keio University · JP

Funding

Chugai Pharmaceutical Co. Ltd.Chugai Pharmaceutical Co., Ltd
6 · The paper itself

Abstract

objectivesAnti-IL-6 receptor antibodies are clinically efficacious in the management of RA with an associated increase in Tregs; however, the role of functional Treg subsets has yet to be clarified. This study aimed to evaluate how functional Treg subsets are altered by IL-6 receptor blockade and to analyse the relationship between these Treg subsets and the clinical outcome of RA.

methodsWe collected frozen peripheral blood mononuclear cells (PBMCs) from 40 patients with RA who started tocilizumab (TCZ) with or without MTX and 11 healthy controls (HCs). We fractionated Tregs with flow cytometry based on markers of phenotype and function and measured the proportions of detailed Treg subsets sequentially from baseline to week 52.

resultsThe proportions of resting Tregs (rTregs) and rTregs+activated Tregs (aTregs) were significantly lower in RA patients at baseline than in HCs. The proportions of all those CD127low Tregs, rTregs, aTregs and rTregs+aTregs were significantly increased with TCZ treatment. In patients treated with TCZ without MTX, rTreg were increased. Patients with an increase in the proportion of rTregs at week 12 had significantly less arthritis flares during the observation period.

conclusionsBlocking the IL-6 receptor with TCZ increased the proportion of rTregs, a functional Treg subpopulation. Patients with an early increase in rTregs showed a favourable treatment course and this increase in rTregs may reflect molecular remission induced by IL-6 signal inhibition.

Indexed as

Antibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, RheumatoidMethotrexateT-Lymphocytes, RegulatoryAdultAgedCase-Control StudiesFemaleFlow CytometryHumansInterleukin-6 InhibitorsMaleMiddle AgedReceptors, Interleukin-6Treatment OutcomeAntibodies, Monoclonal, HumanizedAntirheumatic AgentsInterleukin-6 InhibitorsMethotrexateReceptors, Interleukin-6tocilizumabinterleukin-6regulatory T cellrheumatoid arthritistocilizumab

Identifiers

PMID38530780
PMCPMC11371379
OpenAlexW4393185965

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Registered trials

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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.