Evidence map›Paper›PMID 24550909›Full record

ArticleFrontiers in immunology2014

Immunological Outcome in Haploidentical-HSC Transplanted Patients Treated with IL-10-Anergized Donor T Cells.

Rosa Bacchetta, Barbarella Lucarelli, Claudia Sartirana, Silvia Gregori, Maria T Lupo Stanghellini, Patrick Miqueu, Stefan Tomiuk, Maria Hernandez-Fuentes, Monica E Gianolini, Raffaella Greco and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

81 citing papers in PubMed, 140 citations in OpenAlex.

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  17. Highly purified and functionally stableFrontiers in immunology · 2023
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21 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

19 authors at 6 institutions in 4 countries.

Rosa BacchettaDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy.
Barbarella LucarelliDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy.
Claudia SartiranaDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy.
Silvia GregoriDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy.
Maria T Lupo StanghelliniHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Patrick MiqueuTcLand Expression S. A. , Nantes , France.
Stefan TomiukMiltenyi Biotec GmbH , Bergisch-Gladbach , Germany.
Maria Hernandez-FuentesMRC Center for Transplantation, King's College London , London , UK.
Monica E GianoliniDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy.
Raffaella GrecoHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Massimo BernardiHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Elisabetta ZapponeHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Silvano RossiniUnit of Immunohaematology and Transfusion Medicine Service, San Raffaele Hospital , Milan , Italy.
Uwe JanssenMiltenyi Biotec GmbH , Bergisch-Gladbach , Germany.
Alessandro AmbrosiCenter for Statistics in Biomedical Sciences, San Raffaele Scientific Institute , Milan , Italy.
Monica SalomoniMolMed SpA , Milan , Italy.
Jacopo PeccatoriHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Fabio CiceriHematology and BMT Unit, San Raffaele Hospital , Milan , Italy.
Maria-Grazia RoncaroloDivision of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, San Raffaele Telethon Institute for Gene Therapy , Milan , Italy ; Vita-Salute San Raffaele University , Milan , Italy.
The San Raffaele Telethon Institute for Gene Therapy · ITMiltenyi Biotec (Germany) · DEExpression Génétique Microbienne · FRKing's College London · GBMolMed (Italy) · ITVita-Salute San Raffaele University · IT

Funding

Medical Research Council G0600698Medical Research Council G0801537Medical Research Council MR/J006742/1Telethon TGT11A04
6 · The paper itself

Abstract

T-cell therapy after hematopoietic stem cell transplantation (HSCT) has been used alone or in combination with immunosuppression to cure hematologic malignancies and to prevent disease recurrence. Here, we describe the outcome of patients with high-risk/advanced stage hematologic malignancies, who received T-cell depleted (TCD) haploidentical-HSCT (haplo-HSCT) combined with donor T lymphocytes pretreated with IL-10 (ALT-TEN trial). IL-10-anergized donor T cells (IL-10-DLI) contained T regulatory type 1 (Tr1) cells specific for the host alloantigens, limiting donor-vs.-host-reactivity, and memory T cells able to respond to pathogens. IL-10-DLI were infused in 12 patients with the goal of improving immune reconstitution after haplo-HSCT without increasing the risk of graft-versus-host-disease (GvHD). IL-10-DLI led to fast immune reconstitution in five patients. In four out of the five patients, total T-cell counts, TCR-Vβ repertoire and T-cell functions progressively normalized after IL-10-DLI. These four patients are alive, in complete disease remission and immunosuppression-free at 7.2 years (median follow-up) after haplo-HSCT. Transient GvHD was observed in the immune reconstituted (IR) patients, despite persistent host-specific hypo-responsiveness of donor T cells in vitro and enrichment of cells with Tr1-specific biomarkers in vivo. Gene-expression profiles of IR patients showed a common signature of tolerance. This study provides the first indication of the feasibility of Tr1 cell-based therapy and paves way for the use of these Tr1 cells as adjuvant treatment for malignancies and immune-mediated disorders.

Indexed as

cell therapyhaploidenticalhematopoietic stem cell transplantationIL-10toleranceT regulatory type 1 cells

Identifiers

PMID24550909
PMCPMC3907718
OpenAlexW2116169090

What OpenQuestion holds

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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.