Evidence map›Paper›PMID 37531660›Full record

ArticleBlood advances2023

Sézary syndrome originates from heavily mutated hematopoietic progenitors.

Carly M Harro, Kimberly B Sprenger, Ricardo A Chaurio, John J Powers, Patrick Innamarato, Carmen M Anadon, Yumeng Zhang, Subir Biswas, Gunjan Mandal, Jessica A Mine and 10 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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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

20 authors at 4 institutions in 2 countries.

Carly M HarroDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-0683-217X
Kimberly B SprengerDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-8711-9068
Ricardo A ChaurioDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
John J PowersDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0003-3800-2645
Patrick InnamaratoDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Carmen M AnadonDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Yumeng ZhangDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Subir BiswasDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Gunjan MandalDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Jessica A MineDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Carla CortinaDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-4353-4008
Mate Z NagyDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0001-5845-0926
Alexandra L MartinDepartment of Gynecologic Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Katelyn F HandleyDepartment of Gynecologic Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-3020-5731
Gustavo J BorjasDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-8857-0299
Pei-Ling ChenDepartment of Pathology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Javier Pinilla-IbarzDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Lubomir SokolDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Xiaoqing YuDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Jose R Conejo-GarciaDepartment of Immunology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Moffitt Cancer Center · USDuke University · USTata Memorial Hospital · INUniversity of South Florida · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
Vascular Leukocytes Influence the Tumor MicroenvironmentR01CA124515 · NCI · WISTAR INSTITUTE · PI Jose R Conejo-Garcia · 2007 to 2026
$7.1M
Initiation and Evolution of the Ovarian Cancer MicroenvironmentR01CA157664 · NCI · WISTAR INSTITUTE · PI CONEJO-GARCIA, JOSE R · 2011 to 2020
$3.8M
Targetable epigenetic mechanism driving Cutaneous T cell LymphomaR01CA240434 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CONEJO-GARCIA, JOSE R, PINILLA, JAVIER · 2019 to 2023
$2.6M
Spontaneous humoral responses open opportunities for novel immunotherapies against human cancerK99CA266947 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BISWAS, SUBIR · 2022 to 2023
$215k
NCI NIH HHS K99 CA266947NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA124515NCI NIH HHS R01 CA157664NCI NIH HHS R01 CA240434
6 · The paper itself

Abstract

The pathogenesis of cutaneous T-cell lymphoma (CTCL) remains unclear. Using single-cell RNA or T-cell receptor (TCR) sequencing of 32 619 CD3+CD4+ and CD26+/CD7+ and 29 932 CD3+CD4+ and CD26-/CD7- lymphocytes from the peripheral blood of 7 patients with CTCL, coupled to single-cell ATAC-sequencing of 26,411 CD3+CD4+ and CD26+/CD7+ and 33 841 CD3+CD4+ and CD26-/CD7- lymphocytes, we show that tumor cells in Sézary syndrome and mycosis fungoides (MF) exhibit different phenotypes and trajectories of differentiation. When compared to MF, Sézary cells exhibit narrower repertoires of TCRs and exhibit clonal enrichment. Surprisingly, we identified ≥200 mutations in hematopoietic stem cells from multiple patients with Sézary syndrome. Mutations in key oncogenes were also present in peripheral Sézary cells, which also showed the hallmarks of recent thymic egression. Together our data suggest that CTCL arises from mutated lymphocyte progenitors that acquire TCRs in the thymus, which complete their malignant transformation in the periphery.

Indexed as

Lymphoma, T-Cell, CutaneousMycosis FungoidesSezary SyndromeSkin NeoplasmsDipeptidyl Peptidase 4HumansReceptors, Antigen, T-CellDipeptidyl Peptidase 4Receptors, Antigen, T-Cell

Identifiers

PMID37531660
PMCPMC10514084
OpenAlexW4385479065

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.