Evidence map›Paper›PMID 35136603›Full record

ArticleClinical & translational immunology2022

Allogeneic CD20-targeted γδ T cells exhibit innate and adaptive antitumor activities in preclinical B-cell lymphoma models.

Kevin P Nishimoto, Taylor Barca, Aruna Azameera, Amani Makkouk, Jason M Romero, Lu Bai, Mary M Brodey, Jackie Kennedy-Wilde, Hui Shao, Stephanie Papaioannou and 18 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
10.0field-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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Efficient multiplex non-viral engineering and expansion of polyclonal γδ CAR-T cells for immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  6. Article
  7. Review
  8. Article
  9. Review
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  11. Article
  12. Harnessing Vδ1Frontiers in immunology · 2026
    Review
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  15. Article
  16. Review
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  19. Article
  20. Review

15 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

28 authors at 2 institutions in 1 country.

Kevin P NishimotoAdicet Bio, Inc. Menlo Park CA USA.
Taylor BarcaAdicet Bio, Inc. Menlo Park CA USA.
Aruna AzameeraAdicet Bio, Inc. Menlo Park CA USA.
Amani MakkoukAdicet Bio, Inc. Menlo Park CA USA.
Jason M RomeroAdicet Bio, Inc. Menlo Park CA USA.
Lu BaiAdicet Bio, Inc. Menlo Park CA USA.
Mary M BrodeyAdicet Bio, Inc. Menlo Park CA USA.
Jackie Kennedy-WildeAdicet Bio, Inc. Menlo Park CA USA.
Hui ShaoAdicet Bio, Inc. Menlo Park CA USA.
Stephanie PapaioannouAdicet Bio, Inc. Menlo Park CA USA.
Amy DoanAdicet Bio, Inc. Menlo Park CA USA.
Cynthia MasriAdicet Bio, Inc. Menlo Park CA USA.
Ngoc T HoangAdicet Bio, Inc. Menlo Park CA USA.
Hayden TessmanAdicet Bio, Inc. Menlo Park CA USA.
Vidhya Dhevi RamanathanAdicet Bio, Inc. Menlo Park CA USA.
Ana Giner-RubioAdicet Bio, Inc. Menlo Park CA USA.
Frank DelfinoRegeneron Pharmaceuticals, Inc. Tarrytown NY USA.
Kriti SharmaRegeneron Pharmaceuticals, Inc. Tarrytown NY USA.
Kevin BrayRegeneron Pharmaceuticals, Inc. Tarrytown NY USA.
Matthew HoopesAdicet Bio, Inc. Menlo Park CA USA.
Daulet SatpayevAdicet Bio, Inc. Menlo Park CA USA.
Ranjita SenguptaAdicet Bio, Inc. Menlo Park CA USA.
Marissa HerrmanAdicet Bio, Inc. Menlo Park CA USA.
Stewart E AbbotAdicet Bio, Inc. Menlo Park CA USA.
Blake T AftabAdicet Bio, Inc. Menlo Park CA USA.ORCID https://orcid.org/0000-0003-4020-2718
Zili AnAdicet Bio, Inc. Menlo Park CA USA.
Swapna PanugantiAdicet Bio, Inc. Menlo Park CA USA.
Sandra M HayesAdicet Bio, Inc. Menlo Park CA USA.
Menlo School · USRegeneron (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAutologous chimeric antigen receptor (CAR) αβ T-cell therapies have demonstrated remarkable antitumor efficacy in patients with haematological malignancies; however, not all eligible cancer patients receive clinical benefit. Emerging strategies to improve patient access and clinical responses include using premanufactured products from healthy donors and alternative cytotoxic effectors possessing intrinsic tumoricidal activity as sources of CAR cell therapies. γδ T cells, which combine innate and adaptive mechanisms to recognise and kill malignant cells, are an attractive candidate platform for allogeneic CAR T-cell therapy. Here, we evaluated the manufacturability and functionality of allogeneic peripheral blood-derived CAR

methodsDonor-derived Vδ1 γδ T cells from peripheral blood were

resultsAnti-CD20 CAR

conclusionThese preclinical data support the clinical evaluation of ADI-001, an allogeneic CD20 CAR

Indexed as

adoptive cell therapyB‐cell lymphomaCD20chimeric antigen receptorγδ T cells

Identifiers

PMID35136603
PMCPMC8809437
OpenAlexW4210450192

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.