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035 |a (DE-627)NLM113186584 
035 |a (NLM)11414745 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Chehimi, J  |e verfasserin  |4 aut 
245 1 0 |a Cytokine and chemokine dysregulation in hyper-IgE syndrome 
264 1 |c 2001 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 16.08.2001 
500 |a Date Revised 19.10.2016 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a Copyright 2001 Academic Press. 
520 |a Hyper-IgE syndrome is characterized by severe recurrent staphylococcal infections, eczema, bone abnormalities, and markedly elevated levels of immunoglobulin E (IgE). The genetic basis is not known and the central immunologic defect is largely undefined. Reduced neutrophil chemotaxis is often described, and variable T cell defects have been demonstrated in some patients. It has been hypothesized that hyper-IgE is associated with a Th1/Th2 imbalance. We wished to characterize cytokine and chemokine imbalances that might reflect the underlying disease process or reflect ongoing pathologic processes. Nine patients with hyper-IgE syndrome and six controls were studied. Radioimmunoassays, flow cytometry, and gene array analyses were performed to characterize cytokine and chemokine production. Hyper-IgE patients express more IL-12, while ENA-78, MCP-3, and eotaxin are markedly underexpressed. Underexpression of a set of chemokines could explain a number of features of hyper-IgE syndrome and may offer a new paradigm for the understanding of this disorder 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, P.H.S. 
650 7 |a CCL11 protein, human  |2 NLM 
650 7 |a CCL7 protein, human  |2 NLM 
650 7 |a CXCL5 protein, human  |2 NLM 
650 7 |a Chemokine CCL11  |2 NLM 
650 7 |a Chemokine CCL7  |2 NLM 
650 7 |a Chemokine CXCL5  |2 NLM 
650 7 |a Chemokines  |2 NLM 
650 7 |a Chemokines, CC  |2 NLM 
650 7 |a Chemokines, CXC  |2 NLM 
650 7 |a Cytokines  |2 NLM 
650 7 |a DNA, Complementary  |2 NLM 
650 7 |a Interleukin-8  |2 NLM 
650 7 |a Interleukins  |2 NLM 
650 7 |a Monocyte Chemoattractant Proteins  |2 NLM 
650 7 |a Phytohemagglutinins  |2 NLM 
650 7 |a RNA, Messenger  |2 NLM 
650 7 |a SPP1 protein, human  |2 NLM 
650 7 |a Sialoglycoproteins  |2 NLM 
650 7 |a Tumor Necrosis Factor-alpha  |2 NLM 
650 7 |a Osteopontin  |2 NLM 
650 7 |a 106441-73-0  |2 NLM 
650 7 |a Interleukin-12  |2 NLM 
650 7 |a 187348-17-0  |2 NLM 
650 7 |a Interferon-gamma  |2 NLM 
650 7 |a 82115-62-6  |2 NLM 
650 7 |a Nicotinamide Phosphoribosyltransferase  |2 NLM 
650 7 |a EC 2.4.2.12  |2 NLM 
650 7 |a nicotinamide phosphoribosyltransferase, human  |2 NLM 
650 7 |a EC 2.4.2.12  |2 NLM 
650 7 |a Receptor, trkA  |2 NLM 
650 7 |a EC 2.7.10.1  |2 NLM 
650 7 |a Tetradecanoylphorbol Acetate  |2 NLM 
650 7 |a NI40JAQ945  |2 NLM 
700 1 |a Elder, M  |e verfasserin  |4 aut 
700 1 |a Greene, J  |e verfasserin  |4 aut 
700 1 |a Noroski, L  |e verfasserin  |4 aut 
700 1 |a Stiehm, E R  |e verfasserin  |4 aut 
700 1 |a Winkelstein, J A  |e verfasserin  |4 aut 
700 1 |a Sullivan, K E  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Clinical immunology (Orlando, Fla.)  |d 1999  |g 100(2001), 1 vom: 10. Juli, Seite 49-56  |w (DE-627)NLM098196855  |x 1521-7035  |7 nnns 
773 1 8 |g volume:100  |g year:2001  |g number:1  |g day:10  |g month:07  |g pages:49-56 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_11 
912 |a GBV_ILN_24 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 100  |j 2001  |e 1  |b 10  |c 07  |h 49-56