Enhanced Antitumor Immunity Through T Cell Activation with Optimized Tandem Double-OX40L mRNAs

In conclusion, our findings highlight the therapeutic potential of the optimized diOX40L mRNA cancer agent in cancer treatment and its potential as an innovative alternative to protein-based therapies. The study underscores the significance of mRNA-based agents in modulating the immune microenvironment and enhancing antitumor responses.

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Publication Details

Journal
International Journal of Nanomedicine
Published
2025-03-01
DOI
https://doi.org/10.2147/ijn.s479434
Citations
4
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
4.18
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article

Enhanced Antitumor Immunity Through T Cell Activation with Optimized Tandem Double-OX40L mRNAs

Zhaohai Wang, Yuying Tian, Minggen Hu, Zherui Liu et al.
4 citations
International Journal of Nanomedicine
CAR-T cell therapy research
4.18
article

Enhanced Antitumor Immunity Through T Cell Activation with Optimized Tandem Double-OX40L mRNAs

Zhaohai Wang, Yuying Tian, Minggen Hu, Zherui Liu, Zhuoya Deng, Rong Liu, Penghui Yang, Zhaohui Xiao, Yongru Xu, Jing Wang
article en
4 citations

Abstract

In conclusion, our findings highlight the therapeutic potential of the optimized diOX40L mRNA cancer agent in cancer treatment and its potential as an innovative alternative to protein-based therapies. The study underscores the significance of mRNA-based agents in modulating the immune microenvironment and enhancing antitumor responses.

International Journal of NanomedicineVol. Volume 20
Capital Medical University (CN), Peking University (CN), Chinese PLA General Hospital (CN), Peking University People's Hospital (CN), Beijing YouAn Hospital (CN)
Zero hunger
Openalex Percentile: Top 6%
CAR-T cell therapy research
4.18
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Enhanced Antitumor Immunity Through T Cell Activation with Optimized Tandem Double-OX40L mRNAs — Zhaohai Wang, Yuying Tian, et al. · International Journal of Nanomedicine (2025) | TGRS Research Map | TGRS