Evidence map›Paper›PMID 37735552›Full record

ReviewBritish journal of haematology2023

The role of T cells and myeloid-derived suppressor cells in refractory immune thrombocytopenia.

Karina Yazdanbakhsh, Drew Provan, John W Semple

Open access · greenAbstract readReview
In one paragraph

Review in British journal of haematology, 2023. 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
6.4field-weighted citation impact, top 3% 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, 22 citations in OpenAlex.

  1. Review
  2. The Immunology of Transfusion Medicine: Past, Present, and Future.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  3. Analysis of Galectin Binding to Blood Group Expressing Bacteria.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Refractory ITP: revisiting definitions, diagnostics, and management paradigms.Hematology. American Society of Hematology. Education Program · 2025
    Review
  5. Haemostasis alterations in immune thrombocytopenia and their clinical significance.Research and practice in thrombosis and haemostasis · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. 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

3 authors at 3 institutions in 4 countries.

Karina YazdanbakhshLaboratory of Complement Biology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, USA.ORCID 0000-0002-1968-0101
Drew ProvanDepartment of Haematology, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID 0000-0002-5110-8455
John W SempleDivision of Hematology and Transfusion Medicine, Lund University, Lund, Sweden.ORCID 0000-0002-1510-0077
New York Blood Center · USQueen Mary University of London · GBUniversity of Toronto · CA

Funding

Sickle cell bone marrow niche and regulation of platelet activation and erythropoiesisP01HL149626 · NHLBI · NEW YORK BLOOD CENTER · PI Karina Yazdanbakhsh · 2020 to 2026
$24.4M
Immune Pathophysiology of Sickle Cell DiseaseR35HL161239 · NHLBI · NEW YORK BLOOD CENTER · PI Karina Yazdanbakhsh · 2022 to 2026
$4.5M
NHLBI NIH HHS P01 HL149626NHLBI NIH HHS R35 HL161239
6 · The paper itself

Abstract

Immune thrombocytopenia (ITP) is characterized by a dysregulated immune response against platelets, affecting both their destruction and production. A role for an abnormal T-cell compartment has been established in ITP pathogenesis and treatments that increase platelet counts in patients with ITP have shown improvements in T-cell profiles. On the other hand, patients who were refractory to treatment appear to retain the T-cell abnormalities as before. Myeloid-derived suppressive cells (MDSCs) are also emerging as key contributors to the immune pathology of ITP and response to treatment. In this review, we will discuss how various treatments affect the T-cell and MDSC compartments in ITP. The review will focus on studies that have examined the underlying mechanisms and/or genetic basis responsible for refractoriness to a given treatment and highlight remaining challenges in identifying factors and mechanisms to predict response to treatment.

Indexed as

Myeloid-Derived Suppressor CellsPurpura, Thrombocytopenic, IdiopathicThrombocytopeniaHumansMyeloid CellsT-Lymphocytesmyeloid-derived suppressive cellsrefractory immune thrombocytopeniaresponder/non-responderrole of T cellsthrombopoietin receptor agonistsT regulatory

Identifiers

PMID37735552
PMCPMC11493757
OpenAlexW4386945459

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.