Evidence map›Paper›PMID 37735656›Full record

ReviewJournal of nanobiotechnology2023

Nano-immunotherapy: overcoming delivery challenge of immune checkpoint therapy.

Seyed Hossein Kiaie, Hossein Salehi-Shadkami, Mohammad Javad Sanaei, Marzieh Azizi, Mahdieh Shokrollahi Barough, Mohammad Sadegh Nasr, Mohammad Sheibani

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Journal of nanobiotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
15.6field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
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  13. Embracing cancer immunotherapy with manganese particles.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  14. Application of nanomedicines in tumor immunotherapy.Journal of molecular cell biology · 2025
    Review
  15. Nanocarriers for cutting-edge cancer immunotherapies.Journal of translational medicine · 2025
    Review
  16. Programmed cell death protein 1 in cancer cells.Cell communication and signaling : CCS · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Seyed Hossein KiaieDepartment of Formulation Development, ReNAP Therapeutics, Tehran, Iran. hosseinkiaie@gmail.com.
Hossein Salehi-ShadkamiDepartment of Formulation Development, ReNAP Therapeutics, Tehran, Iran.
Mohammad Javad SanaeiCellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, 8815713471, Iran.
Marzieh AziziInstitute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran.
Mahdieh Shokrollahi BaroughDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, 1449614535, Iran.
Mohammad Sadegh NasrDepartment of Computer Science and Engineering Multi-Interprofessional Center for Health Informatics (MICHI), The University of Texas at Arlington, Arlington, TX, USA.
Mohammad SheibaniDepartment of Pharmacology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. Mohammad.sheibani89@gmail.com.
Iran University of Medical Sciences · IRUniversity of Tehran · IRShahrekord University of Medical Sciences · IRTehran University of Medical Sciences · IRThe University of Texas at Arlington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint (ICP) molecules expressed on tumor cells can suppress immune responses against tumors. ICP therapy promotes anti-tumor immune responses by targeting inhibitory and stimulatory pathways of immune cells like T cells and dendritic cells (DC). The investigation into the combination therapies through novel immune checkpoint inhibitors (ICIs) has been limited due to immune-related adverse events (irAEs), low response rate, and lack of optimal strategy for combinatorial cancer immunotherapy (IMT). Nanoparticles (NPs) have emerged as powerful tools to promote multidisciplinary cooperation. The feasibility and efficacy of targeted delivery of ICIs using NPs overcome the primary barrier, improve therapeutic efficacy, and provide a rationale for more clinical investigations. Likewise, NPs can conjugate or encapsulate ICIs, including antibodies, RNAs, and small molecule inhibitors. Therefore, combining the drug delivery system (DDS) with ICP therapy could provide a profitable immunotherapeutic strategy for cancer treatment. This article reviews the significant NPs with controlled DDS using current data from clinical and pre-clinical trials on mono- and combination IMT to overcome ICP therapeutic limitations.

Indexed as

AntibodiesImmunotherapyCombined Modality TherapyDrug Delivery SystemsImmune Checkpoint InhibitorsAntibodiesImmune Checkpoint InhibitorsChemoimmunotherapyCTLA-4Immune checkpointNanoparticlesPD-1 and PD-L1Tumor microenvironment

Identifiers

PMID37735656
PMCPMC10512572
OpenAlexW4386929113

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.