Evidence map›Paper›PMID 32457754›Full record

ArticleFrontiers in immunology2020

Engineered IL-21 Cytokine Muteins Fused to Anti-PD-1 Antibodies Can Improve CD8+ T Cell Function and Anti-tumor Immunity.

Shanling Shen, Gail Sckisel, Anupama Sahoo, Almin Lalani, Doug Den Otter, Josh Pearson, Jason DeVoss, Jay Cheng, Stephanie C Casey, Ryan Case and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

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

  1. Pooled it
  2. Article
  3. A modular platform for Sterically Masked Activated Cytokines (SMACks).Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. AttenuatedActa pharmaceutica Sinica. B · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Targeting PD-1Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
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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 at 2 institutions in 1 country.

Shanling ShenDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Gail SckiselDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Anupama SahooDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Almin LalaniDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Doug Den OtterDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Josh PearsonPharmacokinetics and Drug Metabolism, Amgen Research, South San Francisco, CA, United States.
Jason DeVossDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Jay ChengDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Stephanie C CaseyDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Ryan CaseDiscovery Attribute Sciences, Amgen Research, South San Francisco, CA, United States.
Melissa YangBiologics Discovery, Amgen Research, Thousand Oaks, CA, United States.
Ray LowBiologics Discovery, Amgen Research, Thousand Oaks, CA, United States.
Mark DarisBiologics Discovery, Amgen Research, Thousand Oaks, CA, United States.
Bin FanBiologics Discovery, Amgen Research, Thousand Oaks, CA, United States.
Neeraj J AgrawalBiologics Discovery, Amgen Research, Thousand Oaks, CA, United States.
Khaled AliDepartments of Oncology Research, Amgen Research, South San Francisco, CA, United States.
Amgen (United States) · USBiolog (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibitors that block the programmed cell death-1 (PD-1) pathway can potentiate endogenous antitumor immunity and have markedly improved cancer survival rates across a broad range of indications. However, these treatments work for only a minority of patients. The efficacy of anti-PD-1 inhibitors may be extended by cytokines, however, the incorporation of cytokines into therapeutic regimens has significant challenges. In their natural form when administered as recombinant proteins, cytokine treatments are often associated with low response rates. Most cytokines have a short half-life which limits their exposure and efficacy. In addition, cytokines can activate counterregulatory pathways, in the case of immune-potentiating cytokines this can lead to immune suppression and thereby diminish their potential efficacy. Improving the drug-like properties of natural cytokines using protein engineering can yield synthetic cytokines with improved bioavailability and tissue targeting, allowing for enhanced efficacy and reduced off-target effects. Using structure guided engineering we have designed a novel class of antibody-cytokine fusion proteins consisting of a PD-1 targeting antibody fused together with an interleukin-21 (IL-21) cytokine

Indexed as

ImmunotherapyAnimalsAntibodies, MonoclonalB7-H1 AntigenCD8-Positive T-LymphocytesDisease Models, AnimalFemaleHumansInterleukin-21InterleukinsMiceMice, Inbred BALB CMice, SCIDNeoplasmsProtein EngineeringRecombinant Fusion ProteinsAntibodies, MonoclonalB7-H1 AntigenInterleukin-21InterleukinsRecombinant Fusion Proteinsbifunctional fusioncancerengineered cytokineIL-21immunotherapyPD-1

Identifiers

PMID32457754
PMCPMC7225340
OpenAlexW3021420642

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.