Evidence map›Paper›PMID 30250191›Full record

ArticleCell death & disease2018

A novel human IL-2 mutein with minimal systemic toxicity exerts greater antitumor efficacy than wild-type IL-2.

Xi Chen, Xiaojie Ai, Chunlian Wu, Heyong Wang, Gang Zeng, Peixin Yang, Gentao Liu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

32 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  15. Article
  16. IL-2-driven CD8Trends in immunology · 2023
    Review
  17. Collagen-Anchored Interleukin-2 and Interleukin-12 Safely Reprogram the Tumor Microenvironment in Canine Soft-Tissue Sarcomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  18. Review
  19. Engineering cytokine therapeutics.Nature reviews bioengineering · 2023
    Review
  20. Article
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

7 authors at 6 institutions in 2 countries.

Xi ChenShanghai Biomed-Union Biotechnology Co. Ltd, Shanghai, China.
Xiaojie AiSchool of Agriculture and Biology, Shanghai Jiaotong University, Shanghai, China.
Chunlian WuShanghai Biomed-Union Biotechnology Co. Ltd, Shanghai, China.
Heyong WangCentral Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Gang ZengDepartment of Urology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Peixin YangDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. pyang@fpi.umaryland.edu.
Gentao LiuShanghai Biomed-Union Biotechnology Co. Ltd, Shanghai, China. liugt@tongji.edu.cn.
Tongji University · CNChina West Normal University · CNShanghai East Hospital · CNShanghai Jiao Tong University · CNUniversity of California, Los Angeles · USUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IL-2 is critical to the activation, growth, and survival of T cells and NK cells, and maintains the delicate balance between auto-immunity and anti-neoplasm surveillance. High IL-2 doses have clear antitumor capabilities, but also have severe side effects that limit its clinical use. Side effects include the vascular leak syndrome (VLS), which results in lung edema and liver damage. Therefore, a new version of IL-2 that does not induce organ toxicity would improve IL-2-based immunotherapy. We conducted a systematic screening by changing one amino acid at a time at the interaction area of IL-2 with its receptor IL-2R to select one particular mutant IL-2, FSD13, in which the proline at position 65 was substituted by lysine (P65L). FSD13 had a greater ability than wild-type IL-2 in stimulating CD4

Indexed as

ImmunotherapyAmino Acid SubstitutionAnimalsAntineoplastic AgentsApoptosisCD8-Positive T-LymphocytesCell ProliferationCoculture TechniquesDisease Models, AnimalDrug DiscoveryHumansInterleukin-2K562 CellsKiller Cells, NaturalLung NeoplasmsLymphocyte ActivationAntineoplastic AgentsInterleukin-2

Identifiers

PMID30250191
PMCPMC6155133
OpenAlexW2892948281

What OpenQuestion holds

Textmetadata
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.