Evidence map›Paper›PMID 41793185›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Nanomedicine Meets Immunotherapy: Advancing Adoptive Cell Therapy with Nanoparticles in the Treatment of Cancer with Sustainability Perspectives.

Erica Frostegård, Tatiana Bobrova, Amalie Leinebø, Thibault Leray, Shayamita Ghosh, Lorena García-Hevia, Chiara Puccinelli, Lorenzo Riccio, Jacopo Sorani, Davide Bonifazi and 10 more

Abstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

20 authors.

Erica FrostegårdCNRS, Immunology, Immunopathology and Therapeutic Chemistry, UPR 3572, University of Strasbourg, Strasbourg, France.
Tatiana BobrovaINSERM UMR 1186, Integrative Tumor Immunology and Immunotherapy, Gustave Roussy, Fac. de Médecine-University Paris-Sud, Université Paris-Saclay, Villejuif, France.
Amalie LeinebøUniversity of Paris City, CNRS, Inserm, NABI, Paris, France.
Thibault LerayTranslational Research Unit, Section for Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
Shayamita GhoshThe Nanomedicine Group, Universidad de Cantabria-Instituto de Investigación Valdecilla-IDIVAL Avda Herrera Oria s/n, Santander, Spain.
Lorena García-HeviaThe Nanomedicine Group, Universidad de Cantabria-Instituto de Investigación Valdecilla-IDIVAL Avda Herrera Oria s/n, Santander, Spain.
Chiara PuccinelliInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Lorenzo RiccioInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Jacopo SoraniSwiss Federal Laboratories for Materials Science and Technology (Empa), Technology and Society Laboratory, St. Gallen, Switzerland.
Davide BonifaziInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Julien CaumartinExosiris, Le Vésinet, France.
Emmanuel DonnadieuINSERM UMR 1186, Integrative Tumor Immunology and Immunotherapy, Gustave Roussy, Fac. de Médecine-University Paris-Sud, Université Paris-Saclay, Villejuif, France.
Florence GazeauUniversity of Paris City, CNRS, Inserm, NABI, Paris, France.
Roland HischierSwiss Federal Laboratories for Materials Science and Technology (Empa), Technology and Society Laboratory, St. Gallen, Switzerland.
Else Marit InderbergTranslational Research Unit, Section for Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
Mónica L FanarragaThe Nanomedicine Group, Universidad de Cantabria-Instituto de Investigación Valdecilla-IDIVAL Avda Herrera Oria s/n, Santander, Spain.
Maria LoustauExosiris, Le Vésinet, France.
Bernd NowackSwiss Federal Laboratories for Materials Science and Technology (Empa), Technology and Society Laboratory, St. Gallen, Switzerland.
Sébastien WälchliTranslational Research Unit, Section for Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.
Cécilia Ménard-MoyonCNRS, Immunology, Immunopathology and Therapeutic Chemistry, UPR 3572, University of Strasbourg, Strasbourg, France.ORCID https://orcid.org/0000-0003-0348-2466

Funding

Agence Nationale de la Recherche ANRCentre National de la Recherche Scientifique CNRSEuropean Regional Development Fund, and IDIVAL DTEC25/02Interdisciplinary Thematic Institute SysChem via IdEx Unistra ANR-10-IDEX-0002L.G.H. PI23/00261Norwegian Health Authority South-East 2025022Research and Innovation Program (Marie Skłodowska-Curie Actions - Doctoral Networks) 101073025Spanish Instituto de Salud Carlos III DTS24/000237 PI22/00030Swiss State Secretariat for Education, Research and Innovation 22.00287
6 · The paper itself

Abstract

Immunotherapy has achieved remarkable clinical success in certain cancers, particularly through adoptive cell therapy (ACT), where T cell engineering with chimeric antigen receptor (CAR) has driven major clinical breakthroughs in the treatment of hematologic malignancies. However, efficacy against solid tumors remains limited due to multiple barriers, including the scarcity of tumor-specific antigens, antigen heterogeneity, immunosuppressive tumor microenvironment, and physical obstruction of T cell infiltration by dense extracellular matrix. Nanoparticle (NP)-based approaches can overcome these obstacles and enhance ACT by improving tumor immunogenicity and vascular permeability, while reducing off-target toxicity to healthy tissues. This review discusses different strategies leveraging NPs to enhance ACT, including the delivery of immunomodulators and chemotherapeutics, NP-mediated hyperthermia, magnetic guidance to improve T cell accumulation in tumors, and in vivo NP-mediated generation and activation of CAR T cells. While prioritizing patient safety is essential, it does not fully reflect the range of risks and challenges associated with novel nanomedicines. In this regard, we discuss how integrating environmental impact assessments early in the development process is crucial for identifying key impact areas of concern and steering innovation towards more sustainable and responsible designs. Finally, we also identify current challenges, and discuss potential solutions and future research directions, including safety and sustainability.

Indexed as

ImmunotherapyImmunotherapy, AdoptiveNanomedicineNanoparticlesNeoplasmsAnimalsHumansReceptors, Chimeric AntigenT-LymphocytesTumor MicroenvironmentReceptors, Chimeric Antigenchimeric antigen receptordrug deliveryimmunomodulatormagnetic hyperthermiaphotothermal therapy

Identifiers

PMID41793185
PMCPMC13292234

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.