In situ tumor cell engineering reverses immune escape to enhance immunotherapy effect DOI Creative Commons
Shujun Liu,

Shijun Yuan,

Meichen Liu

и другие.

Acta Pharmaceutica Sinica B, Год журнала: 2024, Номер 15(1), С. 627 - 641

Опубликована: Сен. 2, 2024

The underlying cause of low response rates to existing immunotherapies is that tumor cells dominate immune escape through surface antigen deficiency and inducing immunosuppressive microenvironment (TIME). Here, we proposed an in situ cell engineering strategy disrupt at the root by restoring MHC-I/tumor-specific complex (MHC-I/TSA) expression promote T-cell recognition silencing CD55 increase ICOSL+ B-cell proportion reverse TIME. A doxorubicin (DOX) dual-gene plasmid (MAC pDNA, encoding both MHC-I/ASMTNMELM CD55-shRNA) coloaded drug delivery system (LCPN@ACD) with targeting charge/size dual-conversion properties was prepared. LCPN@ACD-induced ICD promoted DC maturation enhanced activation infiltration. LCPN@ACD enabled effective MHC-I/TSA on cells, increasing ability killing. downregulated expression, increased B CTLs, reversed TIME, thus greatly improving efficacy αPD-1 CAR-T therapies. application this eliminated source escape, providing new ideas for solving challenges clinical immunotherapy.

Язык: Английский

Metformin-based nanomedicines for reprogramming tumor immune microenvironment DOI
Jieyu Liu, Xiaoling Li, Yinggang Li

и другие.

Theranostics, Год журнала: 2024, Номер 15(3), С. 993 - 1016

Опубликована: Дек. 2, 2024

Immunotherapy has transformed current cancer management, and it achieved significant progress over last decades. However, an immunosuppressive tumor microenvironment (TME) diminishes the effectiveness of immunotherapy by suppressing activity immune cells facilitating immune-evasion. Adenosine monophosphate-activated protein kinase (AMPK), a key modulator cellular energy metabolism homeostasis, gained growing attention in anti-tumor immunity. Metformin is usually considered as cornerstone diabetes its role activating AMPK pathway also been extensively explored therapy although findings on remain inconsistent. nanomedicine formulation found to hold potential reprogramming TME through immunometabolic modulation both cells. This review elaborates foundation via metformin-based nanomedicines, offering valuable insights for next generation therapy.

Язык: Английский

Процитировано

38

Dendrimer-Mediated Generation of a Metal-Phenolic Network for Antibody Delivery to Elicit Improved Tumor Chemo/Chemodynamic/Immune Therapy DOI
Zhiqiang Wang, Yunqi Guo, Gaoming Li

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2025, Номер unknown

Опубликована: Янв. 9, 2025

To simplify the composition and improve efficacy of metal-phenolic network (MPN)-based nanomedicine, herein, we designed an MPN platform to deliver programmed death ligand-1 (PD-L1) antibody (anti-PD-L1) for combined tumor chemo/chemodynamic/immune therapy. Here, generation 5 poly(amidoamine) dendrimers conjugated with gossypol (Gos) through boronic ester bonds were used as a synthetic polyphenol coordinate Mn2+, then complexed anti-PD-L1 obtain nanocomplexes (for short, DPGMA). The prepared DPGMA exhibited good water dispersibility hydrodynamic size 166.3 nm tumor-microenvironment-responsive drug release behavior. integration Gos Mn2+ within resulted in significant inhibition immunogenic cell activation Gos-mediated chemotherapy Mn2+-catalyzed chemodynamic therapy, respectively, thereby leading dendritic maturation due role played mediate stimulator interferon genes (STING) pathway. Moreover, promoted recognition uptake by PD-L1-overexpressed tumors targeting, achieving combinational therapy mouse melanoma model, where immunotherapy modes three parts via chemotherapy/CDT-mediated ICD, Mn2+-mediated STING activation, antibody-mediated immune checkpoint blockade. With Mn2+-endowed r1 relaxivity (1.38 mM–1 s–1), can also be MR imaging. dendrimer-mediated may developed advanced nanomedicine tackle other cancer types.

Язык: Английский

Процитировано

0

Multi‐Slit Diffraction in Scaled Space‐Time DOI Creative Commons
James M. Feagin

Natural Sciences, Год журнала: 2025, Номер unknown

Опубликована: Фев. 18, 2025

ABSTRACT We revisit multi‐slit diffraction with a scaling of space and time to exploit an equivalence wave packets describing quantum free harmonic oscillator (HO) motion. introduce co‐moving frame coordinates define effective, time‐independent, HO potential that confines directs initially displaced along the classical phase oscillator. ‐slit in lab from slits distant detector familiar spreading propagating front is then described as propagation over just quarter cycle confined well. show features are preserved well characterized both near far fields by trajectories space.

Язык: Английский

Процитировано

0

PD-L1 blockade peptide-functionalized NaGdF4 nanodots for efficient magnetic resonance imaging-guided immunotherapy for breast cancer DOI Creative Commons
Zhenzhen Hu,

Yunkai Bao,

Xiaodong Li

и другие.

RSC Advances, Год журнала: 2025, Номер 15(12), С. 9027 - 9033

Опубликована: Янв. 1, 2025

PD-L1 blockade peptide-functionalized NaGdF 4 nanodots were demonstrated as an efficient nanomedicine for the MRI-guided immunotherapy of TNBC.

Язык: Английский

Процитировано

0

Rational Construct of Extracellular Matrix Mimics via Peptide-Co-assembling Nanofibers for Efficient Bone Regeneration DOI
Xiuhui Wang, Mingkui Shen,

Mengze Ma

и другие.

Advanced Fiber Materials, Год журнала: 2025, Номер unknown

Опубликована: Апрель 2, 2025

Язык: Английский

Процитировано

0

Hypoxia-responsive oncolytic conjugate triggers type-II immunogenic cell death for enhanced photodynamic immunotherapy DOI

Maomao Ren,

Xin Sun, Jiayi Lin

и другие.

Journal of Controlled Release, Год журнала: 2025, Номер unknown, С. 113717 - 113717

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Peptide-based drugs in immunotherapy: current advances and future prospects DOI

Dipanjan Karati,

Shreyasi Meur,

Soumi Das

и другие.

Medical Oncology, Год журнала: 2025, Номер 42(5)

Опубликована: Апрель 23, 2025

Язык: Английский

Процитировано

0

Therapeutic peptides: chemical strategies fortify peptides for enhanced disease treatment efficacy DOI Creative Commons
Qingmei Li,

Chao Wen,

Lijuan Qiu

и другие.

Amino Acids, Год журнала: 2025, Номер 57(1)

Опубликована: Май 8, 2025

Язык: Английский

Процитировано

0

PD-L1-targeted polymer-peptide-immune nanomedicine synergizes radiotherapy for durable tumor control DOI

Jincheng Du,

Chuwen Luo,

Ya Liu

и другие.

Bioactive Materials, Год журнала: 2025, Номер 51, С. 531 - 542

Опубликована: Май 22, 2025

Язык: Английский

Процитировано

0

In situ tumor cell engineering reverses immune escape to enhance immunotherapy effect DOI Creative Commons
Shujun Liu,

Shijun Yuan,

Meichen Liu

и другие.

Acta Pharmaceutica Sinica B, Год журнала: 2024, Номер 15(1), С. 627 - 641

Опубликована: Сен. 2, 2024

The underlying cause of low response rates to existing immunotherapies is that tumor cells dominate immune escape through surface antigen deficiency and inducing immunosuppressive microenvironment (TIME). Here, we proposed an in situ cell engineering strategy disrupt at the root by restoring MHC-I/tumor-specific complex (MHC-I/TSA) expression promote T-cell recognition silencing CD55 increase ICOSL+ B-cell proportion reverse TIME. A doxorubicin (DOX) dual-gene plasmid (MAC pDNA, encoding both MHC-I/ASMTNMELM CD55-shRNA) coloaded drug delivery system (LCPN@ACD) with targeting charge/size dual-conversion properties was prepared. LCPN@ACD-induced ICD promoted DC maturation enhanced activation infiltration. LCPN@ACD enabled effective MHC-I/TSA on cells, increasing ability killing. downregulated expression, increased B CTLs, reversed TIME, thus greatly improving efficacy αPD-1 CAR-T therapies. application this eliminated source escape, providing new ideas for solving challenges clinical immunotherapy.

Язык: Английский

Процитировано

0