By Jiri Mestecky, Michael W. Russell, Susan Jackson, Suzanne M. Michalek, Helena TlaskalováHogenová, Jaroslav Sterzl
355 articles prepared less than the subsequent sections:B and T Cells of the Mucosal Immune process: Trafficking and Cytokine law. Nonlymphoid Cells of the Mucosal Immune method: Epithelial Cells, APC, and different telephone kinds. improvement of Mucosal Immunity: Reproductive Tract, Ontogeny, Phylogeny, and Immunodeficiency. Gnotobiology, Environmental, dietary, and Intrinsic components in Mucosal Immunology. constitution, Proteolysis, and serve as of Mucosal Immunoglobulins: mobile Receptors. scientific Immunology, Immunopathology, Immunodeficiency, and Allergology. Microbial, Parasite, and HIV Mucosal Infections. Immunology of the Liver. Oral Immunology and Immunopathology. Autoimmunity, Oral Tolerance, and getting older. persistent irritation, Inflammatory Bowel ailments and Celiac disorder. Induction of Mucosal Immune Responses and Vaccine supply Systems. Index.
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Advances in Mucosal Immunology: Part A
355 articles prepared lower than the next sections:B and T Cells of the Mucosal Immune procedure: Trafficking and Cytokine rules. Nonlymphoid Cells of the Mucosal Immune approach: Epithelial Cells, APC, and different mobile varieties. improvement of Mucosal Immunity: Reproductive Tract, Ontogeny, Phylogeny, and Immunodeficiency.
Extra resources for Advances in Mucosal Immunology: Part A
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M. Calderon, 1659 e. Perez, C. 1. Melendro ORAL lMMUNIZATION AGAINST MUCOSAL CANDIDIASIS IN A MOUSE MODEL............................................................................ 1663 D. l. Challacombe AUTHOR INDEX 1667 SUBJECT INDEX 1677 xliii INDUCTION AND RECALL OF THE SECONDARY IMMUNE RESPONSE ENTIREL Y IN TISSUE CUL TU RE Jaroslav Sterzl, Jaroslava Milerova, Lucie Mackova, and Jiri Travnicek Department of Immunology, Institute of Microbiology, Czech Academy of Sciences, Prague 4, Czech Republic INTRODUCTION Biological systems acquire new information which is stored and retrieved through the mechanisms of memory.
C. Li, V. Stewart, R. W. Alt, Mol. Cell. Biol. 10: 1672(1990). 9. J. Sanchez and 1. Holmgren, Prac. Nat!. Acad. Sei. USA 86:481 (1989). 10. H. Karasuyama and F. Melchers, Eur. Immunol. 18:94 (1988). 11. M. M. Harnett, M. J. Holman, and G. B. Klaus, J. Immunol. 147:3831 (1991). 12. N. Lycke, T. Tsuji, and J. Holmgren, Eur. J. Immunol. 22:2277 (1992). 1. 20 TRANSFORMING GROWTH FACTOR BETA (TGFß) DIRECTS IgAl AND IgA2 SWITCHING IN HUMAN NAIVE B CELLS Francine Briere, 1 Thierry Defrance,2 Beatrice Vanbervliet,l lean-Michel Bridon,l Isabelle Durand, 1 Francoise Rousset,l and lacques Banchereau I I Schering-Plough, Laboratory for Immunological Research, 27 ch.
IgM and IgG Secondary Responses in Tissue Culture and In Vivo The observation that the IgM secondary response in tissue culture exceeded that number of IgG was a surprising. The cellular basis of this phenomenon was analyzed by transferring isolated B-MC into tissue cultures, into SCID mice, and into diffusion chambers (Fig. 5); under these conditions the IgM response prevailed. The same donors from which 3 8,000 6,000 fi a.. 4,000 2,000 seiD mlc. IgM (JlgG 300 '00 10 6 10 Doses 01 antigen (SRBC) Figure 6.