Electronic Resource

Selective tumor antigen vaccine delivery to human CD169+ antigen-presenting cells using ganglioside-liposomes

التفاصيل البيبلوغرافية
العنوان: Selective tumor antigen vaccine delivery to human CD169+ antigen-presenting cells using ganglioside-liposomes
المؤلفون: Affandi, Alsya J, Grabowska, Joanna, Olesek, Katarzyna, Lopez Venegas, Miguel, Barbaria, Arnaud, Rodríguez, Ernesto, Mulder, Patrick P G, Pijffers, Helen J, Ambrosini, Martino, Kalay, Hakan, O'Toole, Tom, Zwart, Eline S, Kazemier, Geert, Nazmi, Kamran, Bikker, Floris J, Stöckl, Johannes, van den Eertwegh, Alfons J M, de Gruijl, Tanja D, Storm, Gert, van Kooyk, Yvette, den Haan, Joke M M
المصدر: Proceedings of the National Academy of Sciences of the United States of America vol.117 (2020) date: 2020-11-02 nr.44 p.27528-27539 [ISSN 0027-8424]
بيانات النشر: 2020
نوع الوثيقة: Electronic Resource
مستخلص: Priming of CD8+ T cells by dendritic cells (DCs) is crucial for the generation of effective antitumor immune responses. Here, we describe a liposomal vaccine carrier that delivers tumor antigens to human CD169/Siglec-1+ antigen-presenting cells using gangliosides as targeting ligands. Ganglioside-liposomes specifically bound to CD169 and were internalized by in vitro-generated monocyte-derived DCs (moDCs) and macrophages and by ex vivo-isolated splenic macrophages in a CD169-dependent manner. In blood, high-dimensional reduction analysis revealed that ganglioside-liposomes specifically targeted CD14+ CD169+ monocytes and Axl+ CD169+ DCs. Liposomal codelivery of tumor antigen and Toll-like receptor ligand to CD169+ moDCs and Axl+ CD169+ DCs led to cytokine production and robust cross-presentation and activation of tumor antigen-specific CD8+ T cells. Finally, Axl+ CD169+ DCs were present in cancer patients and efficiently captured ganglioside-liposomes. Our findings demonstrate a nanovaccine platform targeting CD169+ DCs to drive antitumor T cell responses.
مصطلحات الفهرس: Siglec-1, CD169, dendritic cells, CD8+ T cells, vaccination, Gangliosides, Humans, Immunogenicity, Vaccine, Leukocytes, Mononuclear, Liposomes, Macrophages/immunology, Neoplasms/immunology, Primary Cell Culture, Proto-Oncogene Proteins/metabolism, Receptor Protein-Tyrosine Kinases/metabolism, Sialic Acid Binding Ig-like Lectin 1/metabolism, THP-1 Cells, Vaccination/methods, Vaccines, Subunit/administration & dosage, Article
URL: https://research-portal.uu.nl/en/publications/c76b00a3-3485-4423-801b-ece26acc545f
https://dspace.library.uu.nl/bitstream/handle/1874/411301/27528.full.pdf?sequence=1
https://dspace.library.uu.nl/bitstream/handle/1874/411301/27528.full.pdf?sequence=1
الاتاحة: Open access content. Open access content
info:eu-repo/semantics/openAccess
ملاحظة: DOI: 10.1073/pnas.2006186117
English
Other Numbers: QGJ oai:research-portal.uu.nl:publications/c76b00a3-3485-4423-801b-ece26acc545f
1445817739
المصدر المساهم: UNIVERSITEIT UTRECHT
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رقم الانضمام: edsoai.on1445817739
قاعدة البيانات: OAIster