Evidence map›Paper›PMID 41824575›Full record

ArticleScience advances2026

IL-7/IL-15/IL-21 cytokine-fusion scaffold generates highly functional CAR T cells enriched in long-lived T memory stem cells.

Erin B Cole, Sara Lamcaj, Agnes V Sydenstricker, Adilyn G Voss, Christopher R Hiner, Hong B Hur, Manoj Kandpal, Natalia Valderrama Pena, Jian Hua Zheng, Ying Xiong and 6 more

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
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  6. Review
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.

Erin B ColeDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0009-0004-9590-8966
Sara LamcajDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0001-8842-4518
Agnes V SydenstrickerDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Adilyn G VossDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Christopher R HinerDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0001-7983-5833
Hong B HurRUH Bioinformatics, Center for Clinical and Translational Science, Rockefeller University Hospital, New York, NY 10065, USA.ORCID 0000-0002-4088-9188
Manoj KandpalRUH Bioinformatics, Center for Clinical and Translational Science, Rockefeller University Hospital, New York, NY 10065, USA.
Natalia Valderrama PenaHCW Biologics Inc., Miramar, FL 33025, USA.ORCID 0009-0005-3117-7487
Jian Hua ZhengDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Ying XiongCaring Cross, Gaithersburg, MD 20878, USA.ORCID 0000-0001-7412-1727
Zhongyu ZhuCaring Cross, Gaithersburg, MD 20878, USA.
Cheng Cheng ZhangDepartment of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0003-4763-3887
Niraj ShresthaHCW Biologics Inc., Miramar, FL 33025, USA.ORCID 0000-0003-3115-6940
Boro DropulicHCW Biologics Inc., Miramar, FL 33025, USA.ORCID 0000-0002-3861-7677
Hing C WongHCW Biologics Inc., Miramar, FL 33025, USA.ORCID 0000-0002-6865-4313
Harris GoldsteinDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.ORCID 0000-0003-0543-6025

Funding

Amplifying and Redirecting CMV-specific CD8 T cells to provide sustained control of HIV infectionR01AI172607 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ALMO, STEVEN C., GOLDSTEIN, HARRIS · 2022 to 2025
$4.4M
Developing and evaluating cell-specific lentivectors capable of selective in vivo generation of anti-HIV T cells to cure HIVR01AI174275 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI HARRIS GOLDSTEIN · 2024 to 2026
$2.2M
Reprogramming myeloid cells to inhibit cancer developmentR01CA263079 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHENGCHENG ZHANG · 2022 to 2026
$1.9M
NCI NIH HHS R01 CA263079NIAID NIH HHS R01 AI172607NIAID NIH HHS R01 AI174275
6 · The paper itself

Abstract

Functional persistence of chimeric antigen receptor T cells (CAR T cells) is limited by conventional CAR T cell manufacturing using anti-CD3/CD28 (αCD3/28) stimulation, which generates terminally differentiated and shorter-lived CAR T cells. We demonstrated that HCW9206, a unique protein scaffold linking interleukin-7 (IL-7), an IL-15/IL-15 receptor α (IL-15Rα) complex, and IL-21, generates CAR T cells without requiring αCD3/28 activation, which are highly enriched in long-lived T memory stem cells (T

Indexed as

Interleukin-15Interleukin-7InterleukinsMemory T CellsReceptors, Chimeric AntigenAnimalsHIV InfectionsHumansImmunologic MemoryImmunotherapy, AdoptiveInterleukin-21MiceInterleukin-15Interleukin-21Interleukin-7InterleukinsReceptors, Chimeric Antigen

Identifiers

PMID41824575
PMCPMC12985740

What OpenQuestion holds

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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.