Evidence map›Paper›PMID 32005809›Full record

ArticleNature communications2020

Persistence of adoptively transferred T cells with a kinetically engineered IL-2 receptor agonist.

Giulia Parisi, Justin D Saco, Felix B Salazar, Jennifer Tsoi, Paige Krystofinski, Cristina Puig-Saus, Ruixue Zhang, Jing Zhou, Gardenia C Cheung-Lau, Alejandro J Garcia and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

61 citing papers in PubMed, 94 citations in OpenAlex.

  1. Trial
  2. Bempegaldesleukin Plus Nivolumab in First-Line Metastatic Melanoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
    Trial
  3. Article
  4. Review
  5. Review
  6. An Engineered Soluble Single-Chain TCR Engager for KRAS-G12V Specific Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Article
  8. The role of exosomes in bladder cancer immunotherapy.Journal of the National Cancer Center · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. PD-L1Frontiers in immunology · 2025
    Article
  16. Proteomics appending a complementary dimension to precision oncotherapy.Computational and structural biotechnology journal · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Article

1 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

21 authors at 6 institutions in 1 country.

Giulia ParisiDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Justin D SacoDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Felix B SalazarDepartment of Medical and Molecular Pharmacology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Jennifer TsoiDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Paige KrystofinskiDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Cristina Puig-SausDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Ruixue ZhangDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Jing ZhouIsoplexis Corporation, Branford, CT, USA.
Gardenia C Cheung-LauDepartment of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Alejandro J GarciaDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Catherine S GrassoDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Richard TavaréRegeneron Pharmaceuticals, Inc., Tarrytown, NY, USA.
Siwen Hu-LieskovanDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Sean MackayIsoplexis Corporation, Branford, CT, USA.
Jonathan ZalevskyNektar Therapeutics, San Francisco, CA, USA.
Chantale BernatchezDepartment of Melanoma Medical Oncology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adi DiabDepartment of Melanoma Medical Oncology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Anna M WuDepartment of Medical and Molecular Pharmacology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0001-8487-823X
Begoña Comin-AnduixDepartment of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Deborah CharychNektar Therapeutics, San Francisco, CA, USA.
Antoni RibasDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. aribas@mednet.ucla.edu.ORCID http://orcid.org/0000-0003-3669-8458
University of California, Los Angeles · USIsoPlexis (United States) · USNektar Therapeutics (United States) · USThe University of Texas MD Anderson Cancer Center · USRegeneron (United States) · USUniversity of Southern California · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTON, PETER A · 1991 to 2018
$39.9M
Project 3: Modeling and overcoming resistance to melanoma immunotherapyP01CA244118 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MORICEAU, GATIEN P · 2020 to 2024
$12.8M
Next Generation Cancer Immunotherapies to Defeat MelanomaR35CA197633 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTONI RIBAS · 2015 to 2026
$10.4M
UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
TARGETED COMBINATORIAL TREATMENT OF BRAF MELANOMASP01CA168585 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RIBAS, ANTONI · 2013 to 2017
$8.4M
NCI NIH HHS P01 CA168585NCI NIH HHS P01 CA244118NCI NIH HHS P30 CA016042NCI NIH HHS R35 CA197633NCI NIH HHS T32 CA009120NIAID NIH HHS P30 AI028697
6 · The paper itself

Abstract

Interleukin-2 (IL-2) is a component of most protocols of adoptive cell transfer (ACT) therapy for cancer, but is limited by short exposure and high toxicities. NKTR-214 is a kinetically-engineered IL-2 receptor βγ (IL-2Rβγ)-biased agonist consisting of IL-2 conjugated to multiple releasable polyethylene glycol chains resulting in sustained signaling through IL-2Rβγ. We report that ACT supported by NKTR-214 increases the proliferation, homing and persistence of anti-tumor T cells compared to ACT with IL-2, resulting in superior antitumor activity in a B16-F10 murine melanoma model. The use of NKTR-214 increases the number of polyfunctional T cells in murine spleens and tumors compared to IL-2, and enhances the polyfunctionality of T and NK cells in the peripheral blood of patients receiving NKTR-214 in a phase 1 trial. In conclusion, NKTR-214 may have the potential to improve the antitumor activity of ACT in humans through increased in vivo expansion and polyfunctionality of the adoptively transferred T cells.

Indexed as

Adoptive TransferAnimalsHumansInterleukin-2Lymphocyte ActivationMelanomaMelanoma, ExperimentalMiceMice, Inbred C57BLPolyethylene GlycolsReceptors, Interleukin-2T-LymphocytesbempegaldesleukinInterleukin-2Polyethylene GlycolsReceptors, Interleukin-2

Identifiers

PMID32005809
PMCPMC6994533
OpenAlexW3003503441

What OpenQuestion holds

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LicenceCC BY
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.