Evidence map›Paper›PMID 41800025›Full record

ReviewImmune network2026

Advances in IL-2 Family Cytokine-Based Cancer Therapies: Overcoming Challenges Through Molecular Engineering and Delivery Strategies.

Hyunseo An, Jiwon Oh, Joonbeom Bae

Abstract readReview
In one paragraph

Review in Immune network, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Precision Genome Engineering in Human Disease: Expanding Therapeutic Roles of CRISPR Technologies.Nigerian medical journal : journal of the Nigeria Medical Association
    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

3 authors.

Hyunseo AnDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.ORCID https://orcid.org/0009-0007-5769-7768
Jiwon OhDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.ORCID https://orcid.org/0009-0009-7918-6672
Joonbeom BaeDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.ORCID https://orcid.org/0000-0002-2502-9147

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokines of the common γ-chain family (IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21) are pivotal in regulating immune responses and hold significant promise for cancer immunotherapy. However, their clinical efficacy has been hindered by short serum half-life, pleiotropic off-target effects, and dose-limiting systemic toxicities such as cytokine release syndrome. This review provides a comprehensive overview of recent advancements designed to overcome these limitations. Molecular engineering strategies, including PEGylation, Fc-fusion, muteins, and next-generation approaches like pro-cytokines and split-cytokines, which aim to enhance stability and receptor specificity. To minimize systemic toxicity and achieve high, tumor-localized cytokine concentrations, a variety of innovative delivery systems have been developed, ranging from polymer- and lipid-based nanoparticles to biological vehicles such as oncolytic viruses and cell-based therapies. Furthermore, these delivery systems are designed to respond to both intrinsic and extrinsic stimuli, enabling spatial and temporal control over cytokine activity. By synthesizing current progress and remaining challenges, this review outlines the future trajectory of cytokine-based therapeutics in achieving precise and safe anti-tumor immunity.

Indexed as

CytokinesDrug delivery systemsIL-2ImmunotherapyT lymphocytesTumor microenvironment

Identifiers

PMID41800025
PMCPMC12962837

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.