Evidence map›Paper›PMID 28723576›Full record

ArticleCell reports2017

An Atlas of Human Regulatory T Helper-like Cells Reveals Features of Th2-like Tregs that Support a Tumorigenic Environment.

Leena Halim, Marco Romano, Reuben McGregor, Isabel Correa, Polychronis Pavlidis, Nathali Grageda, Sec-Julie Hoong, Muhammed Yuksel, Wayel Jassem, Rosalind F Hannen and 8 more

Abstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
–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

101 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Cytokines Associated with Activation of CD4International journal of molecular sciences · 2026
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41 more citing papers are in PubMed but not listed here.

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

18 authors.

Leena HalimMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Marco RomanoMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Reuben McGregorMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Isabel CorreaSt. John's Institute of Dermatology, King's College London, Guy's Hospital, SE1 9RT London, UK.
Polychronis PavlidisMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Nathali GragedaMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Sec-Julie HoongMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Muhammed YukselInstitute of Liver Studies and Transplantation, King's College London, King's College Hospital, SE5 9RS London, UK.
Wayel JassemInstitute of Liver Studies and Transplantation, King's College London, King's College Hospital, SE5 9RS London, UK.
Rosalind F HannenCentre for Cell Biology and Cutaneous Research, The Blizard Institute, Barts and the London School of Medicine and Dentistry, E1 2AT London, UK.
Mark OngHistology/Histopathology Laboratory, King's College Hospital, SE5 9RS London, UK.
Olivia MckinneyHistology/Histopathology Laboratory, King's College Hospital, SE5 9RS London, UK.
Bu'Hussain HayeeDepartment of Gastroenterology, King's College Hospital, SE5 9RS London, UK.
Sophia N KaragiannisSt. John's Institute of Dermatology, King's College London, Guy's Hospital, SE1 9RT London, UK.
Nicholas PowellMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK.
Robert I LechlerMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK; King's Health Partners, SE1 9RT London, UK.
Estefania Nova-LampertiMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK. Electronic address: enovalamperti@gmail.com.
Giovanna LombardiMRC Centre for Transplantation, King's College London, Guy's Hospital, SE1 9RT London, UK. Electronic address: giovanna.lombardi@kcl.ac.uk.

Funding

British Heart Foundation RG/13/12/30395British Heart Foundation TG/16/2/32657Medical Research Council MC_PC_14105Medical Research Council MR/J006742/1Medical Research Council MR/L022699/1Medical Research Council MR/L023091/1
6 · The paper itself

Abstract

Regulatory T cells (Tregs) play a pivotal role in maintaining immunological tolerance, but they can also play a detrimental role by preventing antitumor responses. Here, we characterized T helper (Th)-like Treg subsets to further delineate their biological function and tissue distribution, focusing on their possible contribution to disease states. RNA sequencing and functional assays revealed that Th2-like Tregs displayed higher viability and autocrine interleukin-2 (IL-2)-mediated activation than other subsets. Th2-like Tregs were preferentially found in tissues rather than circulation and exhibited the highest migratory capacity toward chemokines enriched at tumor sites. These cellular responses led us to hypothesize that this subset could play a role in maintaining a tumorigenic environment. Concurrently, Th2-like Tregs were enriched specifically in malignant tissues from patients with melanoma and colorectal cancer compared to healthy tissue. Overall, our results suggest that Th2-like Tregs may contribute to a tumorigenic environment due to their increased cell survival, higher migratory capacity, and selective T-effector suppressive ability.

Indexed as

AdultAutocrine CommunicationFemaleHumansInterleukin-2MaleMelanomaTh2 CellsT-Lymphocytes, RegulatoryTumor MicroenvironmentIL2 protein, humanInterleukin-2chemokine receptorimmunoregulationT helper-like regulatory cellstumor immunitytumor immunology

Identifiers

PMID28723576
PMCPMC5529316

What OpenQuestion holds

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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.