Evidence map›Paper›PMID 42569341›Full record

ArticleMolecular therapy. Advances2026

Double activation and low IL-2 manufacturing protocol increase expansion of healthy and patient-derived CAR-Tregs.

Alessia Ugolini, Anna Miceli, Clara Bercher-Brayer, Susanna Cesarano, Barbara Camisa, Pierluigi Carulli, Paolo Monti, Giuseppe Alvise Ramirez, Elisa Bonomi, Laura Rudilosso and 6 more

Abstract read
In one paragraph

Article in Molecular therapy. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Alessia UgoliniExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Anna MiceliExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Clara Bercher-BrayerExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Susanna CesaranoExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Barbara CamisaExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Pierluigi CarulliExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Paolo MontiSan Raffaele Diabetes Research Institute, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Giuseppe Alvise RamirezImmunology, Rheumatology, Allergology and Rare Disease Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Elisa BonomiSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Laura RudilossoSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Lorenzo DagnaImmunology, Rheumatology, Allergology and Rare Disease Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Daniela CesanaSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Raffaella GrecoHematology and Bone Marrow Transplant Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Fabio CiceriVita-Salute San Raffaele University, 20132 Milan, Italy.
Chiara BoniniExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.
Matteo DoglioExperimental Haematology Unit, Division of Immunology, Transplantation and Infectious Diseases (DITID), IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-engineered regulatory T cells (CAR-Tregs) are a promising approach to restore immune tolerance in autoimmune diseases (ADs). However, the low frequency of circulating Tregs, especially in patients with autoimmunity, might limit their applicability as a clinical approach. Thus, an optimal protocol for

Indexed as

adoptive cell therapyCARsCAR-Tregschimeric antigen receptorsengineeringexpansion protocolsmanufacturingregulatory T cellsrestimulationTregs

Identifiers

PMID42569341
PMCPMC13449783

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.