Liposomal Fc Domain Conjugated to a Cancer Vaccine Enhances Both Humoral and Cellular Immunity

التفاصيل البيبلوغرافية
العنوان: Liposomal Fc Domain Conjugated to a Cancer Vaccine Enhances Both Humoral and Cellular Immunity
المؤلفون: Abhishek Vartak, Steven J. Sucheck, Kamal Hossain, Katherine A. Wall
المصدر: ACS Omega, Vol 4, Iss 3, Pp 5204-5208 (2019)
ACS Omega
سنة النشر: 2019
مصطلحات موضوعية: 0303 health sciences, Cellular immunity, biology, Chemistry, General Chemical Engineering, Antigen presentation, General Chemistry, Article, 3. Good health, lcsh:Chemistry, 03 medical and health sciences, 0302 clinical medicine, Immune system, Antibody Isotype, lcsh:QD1-999, Antigen, 030220 oncology & carcinogenesis, Immunology, biology.protein, Cancer vaccine, Antibody, MUC1, 030304 developmental biology
الوصف: Targeted delivery of antigens to antigen-presenting cells (APCs) by utilizing natural anticarbohydrate antibodies is a promising approach for selective uptake and enhanced antigen presentation. Previously, we reported that in the presence of a natural antibody, anti-rhamnose antibody (anti-Rha), the bacterial sugar rhamnose conjugated with liposomal cancer antigen MUC1-Tn enhances antigen presentation by APCs such as dendritic cells by targeting Fc gamma receptors. The idea was to utilize the natural human anti-Rha antibodies present in human serum for targeted delivery of cancer-specific antigens. Recently, we found that the IgG3 antibody isotype was the most prevalent anti-Rha antibody generated in mice immunized with rhamnose-Ficoll (Rha-Ficoll) antigen. In this manuscript, we have conjugated the murine IgG3-Fc with a MUC1-containing cancer vaccine and compared the humoral and cellular immune response to this vaccine with one targeted via the human anti-Rha antibody and to the MUC1 vaccine alone. This Fc approach enhanced antibody production and T-cell proliferation almost to the same level as using the anti-Rha antibody. These results suggest that targeting Fc directly to dendritic cells can be an alternative approach to human anti-Rha for generating effective antigen-primed T-cells.
تدمد: 2470-1343
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8200473e4da5aba128d300384069430f
https://pubmed.ncbi.nlm.nih.gov/30949616
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....8200473e4da5aba128d300384069430f
قاعدة البيانات: OpenAIRE