Biomimetic Nanovaccines Restore Immunosuppressive Tumor Antigen-Presenting Cells via the Saposin-Feeding Strategy DOI
Bingyuan Fei, Miao Yu, Zheng Wang

и другие.

ACS Biomaterials Science & Engineering, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 19, 2024

Cancer cell membrane-derived biomimetic nanovaccines have shown tremendous potential in cancer immunotherapy. However, their efficacy is restricted by the insufficient cross-presentation of membrane-associated antigens. Saposins (SAs), which are vital for membrane vesicle disintegration and antigen presentation, severely deficient antigen-presenting cells (APCs) within tumors. Herein, we propose a complementary strategy increasing via use SAs. Biomimetic were designed using shells to provide comprehensive array tumor-associated antigens reactive oxygen species (ROS)-responsive nanoparticle cores that allowed codelivery cytosine–guanine dinucleotides (CpGs) The ROS-responsive highly internalized APCs, enabled release CpGs SAs endo/lysosomes APCs. Furthermore, increased activation immunosuppressive APCs enhanced T-cell priming delivering Consequently, loaded with not only suppressed tumor growth but also exhibited excellent therapeutic effects combination immune checkpoint blockade strategies. Overall, our study provides insights into development integrating offers promising effective

Язык: Английский

Harnessing hydrodynamics for high-yield production of extracellular vesicles from stem cells spheroids with specific cargo profiling DOI
Solène Lenoir, Elliot Thouvenot,

Giacomo Gropplero

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2025, Номер unknown

Опубликована: Янв. 3, 2025

ABSTRACT This study presents a novel method and device for the hydrodynamic production of extracellular vesicles (EVs) derived from biomimetic multicellular 3D spheroids, enabling high-throughput particle release that is 10 to 20 times higher than in non-stimulated conditions. The facilitates formation spheroids human mesenchymal stem cells (hMSCs), offering an all-in-one approach both spheroid generation EV release. Production are reduced just few hours, with yield further increased by alternating periods high flow recovery sequential approach. Using this system, we explored impact starvation conditions on protein cargo EVs, identifying distinct markers through proteomics. Specifically, stimulation enriched EVs plasma membrane-derived mitochondrial proteins, revealing divergent biogenesis pathways. Importantly, produced exhibited therapeutic properties, demonstrated effects wound healing, angiogenesis, anti-inflammatory responses, some showing enhanced efficacy under stimulation.

Язык: Английский

Процитировано

0

Akkermansia muciniphila extracellular vesicles: function and theranostic potential in disease DOI Creative Commons
Yudi Wang, Wenlong Lin, Shaohuan Wu

и другие.

LabMed discovery., Год журнала: 2025, Номер unknown, С. 100060 - 100060

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Extracellular vesicles in cancer´s communication: messages we can read and how to answer DOI Creative Commons
Alena Semerádtová, Michaela Liegertová, Regina Herma

и другие.

Molecular Cancer, Год журнала: 2025, Номер 24(1)

Опубликована: Март 19, 2025

Abstract Extracellular vesicles (EVs) are emerging as critical mediators of intercellular communication in the tumor microenvironment (TME), profoundly influencing cancer progression. These nano-sized vesicles, released by both and stromal cells, carry a diverse cargo proteins, nucleic acids, lipids, reflecting dynamic cellular landscape mediating intricate interactions between cells. This review provides comprehensive overview biogenesis, composition, functional roles EVs cancer, highlighting their significance basic research clinical applications. We discuss how cells manipulate EV biogenesis pathways to produce enriched with pro-tumorigenic molecules, explore specific contributions key hallmarks such angiogenesis, metastasis, immune evasion, emphasizing role shaping TME driving therapeutic resistance. Concurrently, we submit recent knowledge on can serve valuable source biomarkers for minimally invasive liquid biopsies, its potential, particularly targeted drug delivery vehicles immunomodulatory agents, showcasing promise enhancing efficacy safety treatments. By deciphering messages carried EVs, gain deeper understanding biology develop more effective strategies early detection, therapy, immunotherapy, paving way new era personalized precise medicine potential significantly improve patient outcomes.

Язык: Английский

Процитировано

0

Extracellular Vesicles: Advanced Tools for Disease Diagnosis, Monitoring, and Therapies DOI Open Access
Pedro Lorite, Jorge N. Domínguez, Teresa Palomeque

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 26(1), С. 189 - 189

Опубликована: Дек. 29, 2024

Extracellular vesicles (EVs) are a heterogeneous group of membrane-encapsulated released by cells into the extracellular space. They play crucial role in intercellular communication transporting bioactive molecules such as proteins, lipids, and nucleic acids. EVs can be detected body fluids, including blood plasma, urine, saliva, amniotic fluid, breast milk, pleural ascites. The complexity diversity require robust standardized approach. By adhering to protocols guidelines, researchers ensure consistency, purity, reproducibility isolated EVs, facilitating their use diagnostics, therapies, research. Exosomes microvesicles represent an exciting frontier modern medicine, with significant potential transform diagnosis treatment various diseases important personalized medicine precision therapy. primary objective this review is provide updated analysis significance highlighting mechanisms action exploring applications diseases. Additionally, addresses existing limitations future offering practical recommendations resolve current challenges enhance viability for clinical use. This comprehensive approach aims bridge gap between EV research its application healthcare.

Язык: Английский

Процитировано

3

Emerging Cancer Immunotherapies: Cutting-Edge Advances and Innovations in Development DOI Creative Commons

Monica Maccagno,

Marta Tapparo, Gabriele Saccu

и другие.

Medical Sciences, Год журнала: 2024, Номер 12(3), С. 43 - 43

Опубликована: Авг. 28, 2024

The rise in biological therapies has revolutionized oncology, with immunotherapy leading the charge through breakthroughs such as CAR-T cell therapy for melanoma and B-ALL. Modified bispecific antibodies cells are being developed to enhance their effectiveness further. However, currently relies on a costly ex vivo manufacturing process, necessitating alternative strategies overcome this bottleneck. Targeted viral transduction offers promising avenue but remains under-optimized. Additionally, novel approaches emerging, vaccine boosting of strengthen immune response against tumors, dendritic cell-based vaccines under investigation. Beyond cells, mRNA therapeutics represent another avenue. delivery DNA/RNA using lipid nanoparticles (LNPs) shows potential, LNPs can be directed T cells. Moreover, CRISPR editing demonstrated ability precisely edit genome, enhancing effector function persistence synthetic Enveloped vehicles packaging Cas9 modified offer virus-free method safe effective molecule release. While platform still transduction, from healthy donors or induced pluripotent stem reduce costs, simplify manufacturing, expand treatment patients low-quality use allogeneic cancer gained attraction its potential lower costs broaden accessibility. This review emphasizes critical improving selectivity efficacy immunotherapies, paving way more targeted successful fight cancer.

Язык: Английский

Процитировано

1

Exploring the potential of the convergence between extracellular vesicles and CAR technology as a novel immunotherapy approach DOI Creative Commons

O. Bar,

Angel Porgador, Tomer Cooks

и другие.

Journal of Extracellular Biology, Год журнала: 2024, Номер 3(9)

Опубликована: Сен. 1, 2024

Abstract Cancer therapy is a dynamically evolving field, witnessing the emergence of innovative approaches that offer promising outlook for patients grappling with persistent disease. Within realm therapeutic exploration, chimeric antigen receptor (CAR) T cells as well CAR NK cells, have surfaced novel approaches, each possessing unique attributes and transformative potential. Immune engineered to express CARs recognizing tumour‐specific antigens, shown remarkable promise in treating terminal cancers by combining precision antibody specificity potent cytotoxic function cells. However, their application solid tumours still its nascent stages, presenting major challenges. On same note, distinct immunotherapeutic approach, utilizing on providing advantages safety, manufacturing simplicity, broader scope cancer treatment. Extracellular vesicles (EVs) emerged agents due ability carry crucial biomarkers biologically active molecules, serving vital messengers intercellular communication network. In context cancer, potential EVs lies delivering tumour‐suppressing proteins, nucleic acid components, or targeting drugs precision, thereby redefining paradigm medicine. The fusion technology capabilities has given rise new frontier. EVs, leveraging power alleviate challenges associated live‐cell therapies. are suggested reduce side effects linked cell hold revolutionize penetrance tumours. act carriers pro‐apoptotic molecules RNA enhancing immune responses expanding this review article, we navigate dynamic landscapes, our objective being evaluate comparative efficacy, safety profiles, complexities, clinical applicability.

Язык: Английский

Процитировано

1

Biomimetic Nanovaccines Restore Immunosuppressive Tumor Antigen-Presenting Cells via the Saposin-Feeding Strategy DOI
Bingyuan Fei, Miao Yu, Zheng Wang

и другие.

ACS Biomaterials Science & Engineering, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 19, 2024

Cancer cell membrane-derived biomimetic nanovaccines have shown tremendous potential in cancer immunotherapy. However, their efficacy is restricted by the insufficient cross-presentation of membrane-associated antigens. Saposins (SAs), which are vital for membrane vesicle disintegration and antigen presentation, severely deficient antigen-presenting cells (APCs) within tumors. Herein, we propose a complementary strategy increasing via use SAs. Biomimetic were designed using shells to provide comprehensive array tumor-associated antigens reactive oxygen species (ROS)-responsive nanoparticle cores that allowed codelivery cytosine–guanine dinucleotides (CpGs) The ROS-responsive highly internalized APCs, enabled release CpGs SAs endo/lysosomes APCs. Furthermore, increased activation immunosuppressive APCs enhanced T-cell priming delivering Consequently, loaded with not only suppressed tumor growth but also exhibited excellent therapeutic effects combination immune checkpoint blockade strategies. Overall, our study provides insights into development integrating offers promising effective

Язык: Английский

Процитировано

0