Evidence map›Paper›PMID 35917442›Full record

ArticleBlood2022

Dual antigen-targeted off-the-shelf NK cells show durable response and prevent antigen escape in lymphoma and leukemia.

Frank Cichocki, Jodie P Goodridge, Ryan Bjordahl, Sajid Mahmood, Zachary B Davis, Svetlana Gaidarova, Ramzey Abujarour, Brian Groff, Alec Witty, Hongbo Wang and 10 more

Abstract read
In one paragraph

Article in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

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  18. Rendering NK Cells Antigen-Specific for the Therapy of Solid Tumours.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Frank CichockiDepartment of Medicine, University of Minnesota, Minneapolis, MN.ORCID 0000-0003-3043-0653
Jodie P GoodridgeFate Therapeutics, San Diego, CA.ORCID 0000-0001-7531-6032
Ryan BjordahlFate Therapeutics, San Diego, CA.
Sajid MahmoodFate Therapeutics, San Diego, CA.
Zachary B DavisDepartment of Medicine, University of Minnesota, Minneapolis, MN.
Svetlana GaidarovaFate Therapeutics, San Diego, CA.ORCID 0000-0003-2793-8472
Ramzey AbujarourFate Therapeutics, San Diego, CA.
Brian GroffFate Therapeutics, San Diego, CA.
Alec WittyFate Therapeutics, San Diego, CA.
Hongbo WangDepartment of Medicine, University of Minnesota, Minneapolis, MN.
Katie TuiningaDepartment of Medicine, University of Minnesota, Minneapolis, MN.
Behiye KodalDepartment of Medicine, University of Minnesota, Minneapolis, MN.
Martin FelicesDepartment of Medicine, University of Minnesota, Minneapolis, MN.
Greg BonelloFate Therapeutics, San Diego, CA.
Janel HuffmanFate Therapeutics, San Diego, CA.
Thomas DaileyFate Therapeutics, San Diego, CA.
Tom T LeeFate Therapeutics, San Diego, CA.
Bruce WalcheckDepartment of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN.ORCID 0000-0003-1933-3887
Bahram ValamehrFate Therapeutics, San Diego, CA.ORCID 0000-0002-5917-3585
Jeffrey S MillerDepartment of Medicine, University of Minnesota, Minneapolis, MN.

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI J SUNIL RAO · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GELLER, MELISSA ANN · 2005 to 2025
$38.2M
Viral priming and targeting NK cells against solid tumor malignanciesR35CA197292 · NCI · UNIVERSITY OF MINNESOTA · PI MILLER, JEFFREY S. · 2015 to 2021
$6.2M
Expression of recombinant Fc receptors by engineered NK cells to enhance cancer cell killingR01CA203348 · NCI · UNIVERSITY OF MINNESOTA · PI WALCHECK, BRUCE K, WU, JIANMING · 2016 to 2025
$4.4M
Bcl11b: A Master Transcription Factor Controlling Human NK Cell DevelopmentR01HL155150 · NHLBI · UNIVERSITY OF MINNESOTA · PI CICHOCKI, FRANK · 2021 to 2025
$1.6M
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS R01 CA203348NCI NIH HHS R35 CA197292NHLBI NIH HHS R01 HL155150
6 · The paper itself

Abstract

Substantial numbers of B cell leukemia and lymphoma patients relapse due to antigen loss or heterogeneity after anti-CD19 chimeric antigen receptor (CAR) T cell therapy. To overcome antigen escape and address antigen heterogeneity, we engineered induced pluripotent stem cell-derived NK cells to express both an NK cell-optimized anti-CD19 CAR for direct targeting and a high affinity, non-cleavable CD16 to augment antibody-dependent cellular cytotoxicity. In addition, we introduced a membrane-bound IL-15/IL-15R fusion protein to promote in vivo persistence. These engineered cells, termed iDuo NK cells, displayed robust CAR-mediated cytotoxic activity that could be further enhanced with therapeutic antibodies targeting B cell malignancies. In multiple in vitro and xenogeneic adoptive transfer models, iDuo NK cells exhibited robust anti-lymphoma activity. Furthermore, iDuo NK cells effectively eliminated both CD19+ and CD19- lymphoma cells and displayed a unique propensity for targeting malignant cells over healthy cells that expressed CD19, features not achievable with anti-CAR19 T cells. iDuo NK cells combined with therapeutic antibodies represent a promising approach to prevent relapse due to antigen loss and tumor heterogeneity in patients with B cell malignancies.

Indexed as

LeukemiaNeoplasmsAntigenic Drift and ShiftHumansKiller Cells, Natural

Identifiers

PMID35917442
PMCPMC9918847

What OpenQuestion holds

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Read underepoch 390

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.