Evidence map›Paper›PMID 35475885›Full record

ArticleBlood advances2022

A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease.

Jennifer S Whangbo, Sarah Nikiforow, Haesook T Kim, Jonathan Wahl, Carol G Reynolds, Sharmila C Rai, Soomin Kim, Andrew Burden, Ana C Alho, João F Lacerda and 7 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01937468 (A Phase I Trial of Regulatory T-cells Plus Low-Dose Interleukin-2 for Steroid-Refractory Chronic Graft-versus-Host-Disease), which is not on this map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
4.7field-weighted citation impact, top 4% 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.

NCT01937468 phase1active not recruitingnot on this map

A Phase I Trial of Regulatory T-cells Plus Low-Dose Interleukin-2 for Steroid-Refractory Chronic Graft-versus-Host-Disease

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2013 to 2026Enrolled25ConditionsChronic Graft Versus Host Disease, Chronic GVHD, Complications of Organ Transplant Stem CellsArmsTreg-enriched infusion, Interleukin-2
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  7. Decoding TNF receptor superfamily control of CD4Cell communication and signaling : CCS · 2026
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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

17 authors at 4 institutions in 2 countries.

Jennifer S WhangboDivision of Hematology-Oncology, Boston Children's Hospital, Boston, MA.ORCID 0000-0002-5759-2532
Sarah NikiforowHarvard Medical School, Boston, MA.
Haesook T KimDepartment of Data Sciences, Dana-Farber Cancer Institute, Boston, MA.
Jonathan WahlDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.
Carol G ReynoldsDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.
Sharmila C RaiDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.
Soomin KimDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-8938-2559
Andrew BurdenDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.
Ana C AlhoInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.ORCID 0000-0001-8803-3453
João F LacerdaInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.ORCID 0000-0003-1351-2809
Edwin P AlyeaDivision of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA.
Corey S CutlerHarvard Medical School, Boston, MA.
Vincent T HoHarvard Medical School, Boston, MA.
Joseph H AntinHarvard Medical School, Boston, MA.
Robert J SoifferHarvard Medical School, Boston, MA.
Jerome RitzHarvard Medical School, Boston, MA.
John KorethHarvard Medical School, Boston, MA.
Dana-Farber Cancer Institute · USHarvard University · USUniversity of Lisbon · PTBoston Children's Hospital · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI JENNIFER W MACK · 1985 to 2026
$330.6M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME · 2009 to 2019
$17.5M
Single Cell Analysis and ImmunogeneticsP01HL158505 · NHLBI · DANA-FARBER CANCER INST · PI Corey S Cutler · 2022 to 2026
$15.3M
Single Cell and ImmunogenomicsP01CA229092 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME · 2019 to 2023
$13.8M
NCI NIH HHS P01 CA142106NCI NIH HHS P01 CA229092NCI NIH HHS P30 CA006516NHLBI NIH HHS P01 HL158505
6 · The paper itself

Abstract

Chronic graft-versus-host disease (cGVHD) remains a frequent cause of nonrelapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Despite recent advances, options for steroid-refractory (SR) cGVHD are limited. In previous trials of low-dose interleukin-2 (LD IL-2), the immunomodulatory properties of regulatory T cells (Tregs) have been harnessed to treat SR-cGVHD safely and effectively. In the present study, we combined a single infusion of Treg-enriched lymphocytes (Treg DLI) from the original stem cell donor with in vivo Treg expansion using LD IL-2 (1 × 106 IU/m2 per day for 8 weeks) in 25 adult patients with SR-cGVHD. Treg were not expanded ex vivo. Treg DLI was initiated at 0.1 × 106 cells per kg patient and escalated to a maximum dose of 1 × 106 cells per kg. Treg DLI plus LD IL-2 was well tolerated and led to partial responses (PR) in 5 of 25 patients (20%) after 8 weeks of therapy. Ten additional patients (40%) had stable disease with minor responses not meeting PR criteria. Patients at all dose levels had similar Treg expansion without significant changes in CD4+ conventional T cells or CD8+ T cells. High-throughput sequencing of the T-cell receptor β locus showed selective improvement of Treg diversity. A subset of DLI-derived Treg clones showed preferential expansion at week 8 and long-term persistence 1-year postinfusion. We demonstrate for the first time that infusion of polyclonal healthy donor Tregs followed by expansion with LD IL-2 is safe in patients with SR-cGVHD, thus establishing a foundation for future adoptive Treg therapies in the posttransplant setting. This trial was registered at www.clinicaltrials.gov as #NCT01937468.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationAdultHumansInterleukin-2SteroidsT-Lymphocytes, RegulatoryInterleukin-2Steroids

Identifiers

PMID35475885
PMCPMC9647832
OpenAlexW4225010683

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.