Evidence map›Paper›PMID 42799424›Full record

ReviewPolymer science & technology (Washington, D.C.)2026

Polymeric Materials in Cancer Immunotherapy: Advances, Challenges, and Future Directions.

Cong Wang, Jichuan Zhang, Jiayu Li, Kaiqi Fan, Shiqi Yin, Yong-Guang Yang, Wenbo Yao, Yuning Zhang, Tianmeng Sun

Abstract readReview
In one paragraph

Review in Polymer science & technology (Washington, D.C.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Cong WangKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Jichuan ZhangKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Jiayu LiKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Kaiqi FanKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Shiqi YinKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Yong-Guang YangKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.
Wenbo YaoKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.ORCID https://orcid.org/0000-0002-8488-4450
Yuning ZhangKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.ORCID https://orcid.org/0000-0002-9597-9578
Tianmeng SunKey Laboratory of Organ Regeneration and Transplantation of Ministry of Education, The First Hospital, Jilin University, Changchun, Jilin 130061, China.ORCID https://orcid.org/0000-0003-2261-4532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite revolutionary advances in tumor immunotherapy, its efficacy is often limited by antigen heterogeneity, immune exhaustion, and impaired immune cell infiltration caused by the immunosuppressive tumor microenvironment (TME). Polymer nanocarriers, leveraging their tunable physicochemical properties, modular architecture, and high design flexibility, offer an ideal platform to overcome these bottlenecks. They can not only protect immunotherapeutic agents (e.g., antigens, adjuvants, checkpoint inhibitors) and enable their targeted and controlled release but also enhance antigen presentation, reinvigorate effector immune cell functions, and reprogram the immunosuppressive network through spatiotemporally precise immune regulation. Furthermore, the versatility of polymer platforms empowers various cutting-edge therapeutic modalities, including cancer vaccines, adoptive cell therapies, and oncolytic viruses, demonstrating broad application potential. This review systematically explores the design principles and targeting strategies of polymer materials for tumor immunotherapy, their key roles in modulating anti-tumor immunity, and the core challenges in their clinical translation. Finally, this review envisions a new intelligent research paradigm driven by artificial intelligence (AI)-aided design and validated by clinically relevant systems such as humanized animal models to accelerate the development of next-generation polymer-based immunotherapies.

Indexed as

Immune microenvironment reprogrammingPolymer nanocarriersTargeted deliveryTumor immunotherapy

Identifiers

PMID42799424
PMCPMC13614125

What Socratic holds

Textmetadata
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 Socratic graph.