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Papers, explained in our own words

Every entry summarises what the study set out to test, what it found and why it changes how we design delivery systems. Browse research and reviews or search the collection.

706 articles

Showing 49–55 of 55 articles · Keyword: Cancer immunotherapy Clear keyword

Frontiers in Immunology.2017ReviewDrug Delivery

49. Advanced strategies in immune Modulation of cancer Using Lipid-Based Nanoparticles

Mizrahy S, Hazan-Halevy I, Landesman-Milo D, Ng Bd, Peer D

Current cancer immunotherapy shows promise but fails across many tumour types, likely because single-pathway treatments cannot overcome the complex immunosuppressive tumour microenvironment (TME). Lipid-based nanoparticles (LNPs) may allow simultaneous, temporally coordinated delivery of multiple immune modulators to…

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Journal of Controlled Release2016ReviewNon-viral Gene Delivery

50. Materials for Non-Viral Intracellular Delivery of Messenger RNA Therapeutics

Kevin J. Kauffman, Matthew J. Webber, Daniel G. Anderson

mRNA therapeutics have broad potential for protein replacement therapy, cancer immunotherapy, and genomic engineering, but effective intracellular delivery remains a major challenge. A chemically diverse suite of delivery materials—originally developed for DNA and siRNA transfection—has recently shown promise for…

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Nature Nanotechnology2014ResearchNon-viral Gene Delivery

51. A Carbon Nanotube–Polymer Composite for T-Cell Therapy

Tarek R. Fadel, Fiona A. Sharp, Nalini Vudattu, Ragy Ragheb, Justin Garyu, Dongin Kim, Enping Hong, Nan Li, Gary L. Haller, Lisa D. Pfefferle, Sune Justesen, Kevan C. Herold, Tarek M. Fahmy

Adoptive cell transfer of tumour-specific T cells is a promising cancer immunotherapy, but efficient and economical ex vivo expansion of T cells remains a bottleneck. Artificial antigen-presenting cells (aAPCs) with high surface area and modular design could overcome cost and scalability limits of dendritic…

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Cellular Immunology (Elsevier)2014ResearchNon-viral Gene Delivery

52. PLGA-nanoparticle mediated delivery of anti-OX40 monoclonal antibody enhances anti-tumor cytotoxic T cell responses

Mingshui Chen, Haichao Ouyang, Shangyong Zhou, Jieyu Li, Yunbin Ye

Agonistic anti-OX40 monoclonal antibody (mAb) can enhance anti-tumour immunity in preclinical models, but as monotherapy it showed only marginal activity and no objective clinical responses in a phase I trial. A delivery system that improves T cell access, multivalent OX40 engagement, and sustained release of…

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2014ReviewNon-viral Gene Delivery

53. Nanocarrier-based immunotherapy in cancer management and research

Singh Ms, Bhaskar S.

Cancer immunotherapy can induce specific antitumor immunity, control metastases, and provide immunological memory, but faces barriers including immunosuppressive tumour microenvironments and poor delivery of immunomodulators. Nanocarriers offer a versatile way to deliver antigens, adjuvants, cytokines, antibodies…

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Pharmaceutical Research2011ReviewNon-viral Gene Delivery

54. Cancer Immunotherapy and Nanomedicine

Wei-Yun Sheng, Leaf Huang

The immune system can recognise and kill pre-cancer and cancer cells, but surviving tumour cells learn to escape immune surveillance after immunoselection. Cancer immunotherapy aims to overcome these escape mechanisms. Nanomedicine offers tools—nanodiagnostics and nanobiopharmaceuticals—to deliver antigens…

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Advanced Drug Delivery Reviews2005ReviewNon-viral Gene Delivery

55. PLGA microspheres for improved antigen delivery to dendritic cells as cellular vaccines

Ying Waeckerle-Men And Marcus Groettrup

Dendritic cell (DC)-based vaccines are limited by the short persistence of MHC class I/peptide complexes on the DC surface—often only a few hours—when soluble peptides are loaded exogenously. This short presentation limits CTL activation and vaccine efficacy. The authors investigated biodegradable PLGA microspheres…

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