Evidence map›Paper›PMID 40238916›Full record

ArticleScience translational medicine2025

Preclinical development of anti-CD21 chimeric antigen receptor T cells to treat T cell acute lymphoblastic leukemia.

Nicola Maciocia, Malika Hoekx, Ciaran Acuna, Brandon Wade, Amy Burley, Saumya Ramanayake, Francesco Nannini, Patrycja A Wawrzyniecka, Thaneswari Karpanasamy, Maria Schuldt and 11 more

Abstract read
In one paragraph

Article in Science translational medicine, 2025. 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

21 authors.

Nicola MaciociaDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-3865-3723
Malika HoekxDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0009-0005-7772-2268
Ciaran AcunaDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0009-0002-1765-1929
Brandon WadeDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0009-0003-4015-5269
Amy BurleyDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0003-3074-6439
Saumya RamanayakeDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0003-4718-8728
Francesco NanniniDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0001-9589-5107
Patrycja A WawrzynieckaDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Thaneswari KarpanasamyDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-5109-3695
Maria SchuldtDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0009-0003-8152-485X
Stephanie NgDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0009-0004-2760-9307
Mathieu FerrariAutolus Ltd., Mediaworks, 191 Wood Lane, White City, London W12 7FP, UK.ORCID 0000-0001-8535-7348
Teresa MarafiotiDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0003-1223-6275
Giuseppe GrittiDepartment of Haematology, Ospedale Papa Giovanni XXIII, Piazza OMS 1, 24127 Bergamo, Italy.ORCID 0000-0002-6789-5123
Shimobi OnuohaAutolus Ltd., Mediaworks, 191 Wood Lane, White City, London W12 7FP, UK.
David O'ConnorDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0003-3542-5976
Lydia LeeDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-6092-8949
Marc MansourDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0001-6835-3791
Asim KhwajaDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-6834-5625
Martin PuleDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-8347-9867
Paul MaciociaDepartment of Haematology, Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.ORCID 0000-0002-9757-8073

Funding

Cancer Research UK RCCPOB-NOV22/100002Medical Research Council MR/T000821/1
6 · The paper itself

Abstract

Patients with relapsed/refractory (r/r) T cell acute lymphoblastic leukemia (T-ALL) have a dismal prognosis, highlighting the urgent need for effective therapies. Chimeric antigen receptor (CAR)-T cell approaches targeting pan-T cell antigens may be limited by T cell aplasia and fratricide, necessitating "rescue" allogeneic hematopoietic stem cell transplantation. In this study, we identify CD21, a pan-B cell marker, as a promising target for T-ALL immunotherapy. CD21 is expressed in 50% of T-ALL cases at diagnosis but in fewer than 10% of mature T cells. We observed that CAR-T cells targeting membrane-distal CD21 epitopes were ineffective, likely because of the bulky, glycosylated nature of the antigen. However, when we engineered CAR-T cells to target membrane-proximal CD21 epitopes using an antigen-binding fragment (Fab)-CAR design, we demonstrated robust activity against T-ALL cell lines, primary tumors, and patient-derived xenografts in both in vitro and in vivo models. The enhanced efficacy of this Fab-CAR design was driven by its high stability and reduced surface expression, addressing limitations of traditional CAR constructs. In addition, pharmacological inhibition of the phosphatidylinositol 3-kinase axis up-regulated CD21 expression in T-ALL, further enhancing the potency of anti-CD21 CAR-T cells in vitro and in a patient-derived xenograft in vivo model. This study establishes CD21 as a viable CAR-T target and highlights advances in CAR design for bulky antigens, as well as the potential for pharmacological strategies to augment target expression. Anti-CD21 CAR-T cells represent a promising therapeutic option for improving outcomes for patients with T-ALL.

Indexed as

Precursor T-Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenT-LymphocytesAnimalsCell Line, TumorHumansImmunotherapy, AdoptiveMiceMice, Inbred NODMice, SCIDXenograft Model Antitumor AssaysReceptors, Chimeric Antigen

Identifiers

PMID40238916
PMCPMC7617635

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.