CD23 : a novel multifunctional regulator of the immune system that binds IgE
著者
書誌事項
CD23 : a novel multifunctional regulator of the immune system that binds IgE
(Monographs in allergy, vol. 29)
Karger, 1991
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注記
Includes bibliographical references and index
内容説明・目次
内容説明
This study is devoted to CD23, the 45-kilodalton glycoprotein which is also referred to as the low affinity IgE receptor. International research groups describe multi-functional aspects of soluble CD23 with respect to lymphocyte physiology and discuss its likely role in vivo as well as its signficance in antigen presentation. Following an historical overview, a molecular description of CD23 in both mouse and man is presented. The majority of contributions then concentrate on the function of this molecule where new development reveals its pleiotropic role in immune and haemopoietic regulation. Some papers focus on the potential role of CD23 in regulating IgE synthesis, while others consider its participation in non-IgE-related functions.
目次
- Its discovery and possible functions, H.L. Spiegelberg
- murine CD23/Fc Rll structure and function and comparison with the human counterpart, D.H. Conrad
- CD23/Fc Rll C-type lectin membrane protein with a split personality, H. Gould et al
- human recombinant CD23 (full length and soluble forms) expressed in insect cells bind IgE, K.U. Jansen et al
- the low affinity receptor for IgE on eosinophils and platelets, M. Capron and M. Joseph
- pharmacological modulation of the expression of the low affinity IgE receptor, B. Dugas et al
- regulation of CD23 in allergic diseases, W. Konig et al
- Fc Rll and the activation of B lymphocytes, M.L. Richards and D.H. Katz
- transduction through CD23 different signalling pathways in human B cells and monocytes, J.P. Kolb et al
- role of membrane and soluble CD23 in lymphocyte physiology, J. Gordon et al
- regulation of specific antibody production via CD23, R.H. Stevens et al
- the role of CD23 on early human haematopoietic precursors, M. Mossalayi et al
- CD23 and epithelial cells, G. Rousselet et al.
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