PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
August 6, 2025Frontiers in Medicine16 citationsOpen Access

Clinical trials of nanoparticle-enhanced CAR-T and NK cell therapies in oncology: overcoming translational and clinical challenges - a mini review

View Full Paper
XZXiaoqian ZhaoJXJian XiongDLDanyang Li

Key Points

  • CAR T-cell and NK cell therapies have improved outcomes in hematological malignancies.
  • Nanoparticles enhance immune cell functionality and improve therapeutic delivery in solid tumors.
  • Current clinical trials face regulatory challenges and limitations in design rationales.
  • Advancements in nanotechnology may address key hurdles in immunotherapy translation.

Abstract

Chimeric antigen receptor (CAR) T-cell and natural killer (NK) cell therapeutic approaches have significantly reshaped the immuno-oncology domain for hematological malignancies. These approaches have sustained therapeutic results in patients with treatment-resistant disease and exhibited robust therapeutic efficacy. However, poor immune cell trafficking, tumor-induced immune suppression, and complex ex vivo modification limit their clinical application in solid tumors. The application of nanotechnology has transformed efforts to overcome these limitations by promoting in vivo expression of CARs, enabling tumor-selective immunomodulation, and allowing site-specific dynamic cytokine modulation. This mini review provides critical valuations of the current clinical trials, focusing on the regulatory challenges, design rationale, and translational advances. This article highlights ongoing challenges, recent developments, and future directions for the clinical translation of advanced immunotherapeutic strategies.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Zhao et al. (2025) studied this question.

synapsesocial.com/papers/689a0fa0e6551bb0af8d1770https://doi.org/10.3389/fmed.2025.1655693
Ask AI
Helpful
Bookmark
Share
View Full Paper