An Interleukin 4 (II,-4) Mutant Protein Inhibits both IL-4 or II.-13-induced Human Immunoglobulin G4 (IgG4) and IgE Synthesis and B Cell Proliferation: Support for a Common Component Shared by II,-4 and IL-13 Receptors
نویسندگان
چکیده
L-4 directs mouse and human B cells to produce, respectively, IgG1 and IgE or IgG4 and IgE (1-6) . Recently, we (7) and others (8) cloned and expressed another T cellderived cytokine (IL-13) . As with IL-4, IL-13 induces human B cells to switch to IgG4 and IgE production in an IL-4independent fashion (7-9, 10) . IL-13 shares many other properties with IL-4 . Like IL-4, it has growth-promoting effects on preactivated B cells (7, 9) and it suppresses the production of the proinflammatory rytokines (IL-la, (3, IL-6, IL-8, and TNF-ca) and other monokines (GM-CSF, M-CSF, GCSF, IL-10, and IL-12) by activated monocytes, whereas, it enhances the production of the IL-1R antagonist (10a) . In addition, IL-13 modulates the expression of various surface molecules
منابع مشابه
An interleukin 4 (IL-4) mutant protein inhibits both IL-4 or IL-13- induced human immunoglobulin G4 (IgG4) and IgE synthesis and B cell proliferation: support for a common component shared by IL-4 and IL-13 receptors
Interleukin 4 (IL-4) and IL-13 share many biological functions. Both cytokines promote growth of activated human B cells and induce naive human surface immunoglobulin D+ (sIgD+) B cells to produce IgG4 and IgE. Here we show that a mutant form of human IL-4, in which the tyrosine residue at position 124 is replaced by aspartic acid (hIL-4.Y124D), specifically blocks IL-4 and IL-13-induced prolif...
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تاریخ انتشار 2003