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Titlebook: Dendritic Cells in Fundamental and Clinical Immunology; Volume 3 Paola Ricciardi-Castagnoli Book 1997 The Editor(s) (if applicable) and The

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書目名稱Dendritic Cells in Fundamental and Clinical Immunology
副標(biāo)題Volume 3
編輯Paola Ricciardi-Castagnoli
視頻videohttp://file.papertrans.cn/266/265519/265519.mp4
叢書名稱Advances in Experimental Medicine and Biology
圖書封面Titlebook: Dendritic Cells in Fundamental and Clinical Immunology; Volume 3 Paola Ricciardi-Castagnoli Book 1997 The Editor(s) (if applicable) and The
描述These proceedings contain selected contributions from the participants to the Fourth International Symposium on Dendritic cells that was held in Venice (Lido) Italy, from Oc- tober 5 to 10, 1996. The symposium was attended by more than 500 scientists coming from 24 different countries. Studies on dendritic cells (DC) have been greatly hampered by the difficulties in preparing sufficient cell numbers and in a reasonable pure form. At this meeting it has been shown that large quantities of DC can be generated from precursors in both mice and humans, and this possibility has enormously encouraged studies aimed to characterize DC physiology and DC-specific genes, and to employ DC therapeutically as adjuvants for im- munization. The possibility of generating large numbers of autologous DC that can be used in the manipulation of the immune response against cancer and infectious diseases has tremendously boosted dendritic cell research and the role of DC in a number of medi- cal areas has been heatedly discussed.
出版日期Book 1997
關(guān)鍵詞Antigen; HIV; infections; infectious disease; interferon; physiology
版次1
doihttps://doi.org/10.1007/978-1-4757-9966-8
isbn_softcover978-1-4757-9968-2
isbn_ebook978-1-4757-9966-8Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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https://doi.org/10.1007/978-3-031-35260-7 and maturation of LC cultured by other investigators, would be essential. Our efforts were ultimately rewarded by the development of stable DC lines, termed the “XS series”, from specimens of epidermis in newborn BALB/c mice (1). These XS DC lines resemble resident LC in many respects, including: a
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Johannes K?stler,Sven Gebauer,Hans P. Reiserestion whether marginal DC are capable of endocytosing particulate antigens ., since the spleen is important in the initiation of immune responses against circulating antigens. In immature developmental stages, DC may show uptake of solutes by means of macropinocytosis, but their phagocytic capaciti
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0065-2598 ses has tremendously boosted dendritic cell research and the role of DC in a number of medi- cal areas has been heatedly discussed.978-1-4757-9968-2978-1-4757-9966-8Series ISSN 0065-2598 Series E-ISSN 2214-8019
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CD34+ Hematopoietic Progenitors from Human Cord Blood Differentiate Along two Independent Dendritic ures with CD40-activated naive B cells only the CD 14. derived DC can induced the production of IgM in presence of IL-2. These results suggest that the CD14-derived DC type might be preferentially involved in development of humoral responses, while both populations can induce T cell priming.
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