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Titlebook: In Vivo Immunology; Regulatory Processes E. Heinen,M. P. Defresne,V. Geenen Book 1994 The Editor(s) (if applicable) and The Author(s), unde

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In Vivo Antigen Presentation Capacity of Dendritic Cells from Oral Mucosa and Skin Draining Lymph Nonal lymph nodes. Using fluoresceinated antigen, it has been possible to identify the cells within the population of interdigitating dendritic cells (DC) which are extremely potent antigen presenting cells [1,2]. No B-cells, T-cells or macrophages were bearing detectable levels of antigen [3].
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Analysis by in Situ Hybridization of Cytokine Mrnas Expression in Thymic Nurse Cells isolated from foetuses of CBA mice (Carding et al., 1989). Later on, we demonstrated on frozen sections that mRNAs for IL-1, IL-2, IL-4, IL-6, TNFά and γIFN were present in the thymus during ontogeny following a chronological sequence (Deman. et al., 1992, 1993).
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Book 1994s refer to these conferences as the "Germinal Centre Conferences or GCC". In the 1960s, the germinal centres were the subject of such considerable study and speculation that a group of dynamic people decided to devote an international conference centered on that topic. This led to the fIrst GCC orga
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Thymic Neuroendocrine Self Peptides and t Cell Selectiono-cell signaling in specialized microenvironments constituted by large “nursing” epithelial cells (like TEC/TNC in the thymus, or Sertoli cells in the testis) enclosing cell populations that migrate and differentiate at their very close contact (respectively, T cells and spermatids).. In the general
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Towards Identification of Memory B Cells in Human Tonsilsated from tonsils and found that expression of CD10, CD38 and CD44 distinguished two major B cell subsets among the IgD- B cell compartment. We subsequently separated the two B cell types and performed further phenotypical analysis and functional studies which showed that one of these IgD- B cell po
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