|
|
|
|
LEADER |
01000caa a22002652 4500 |
001 |
NLM155173553 |
003 |
DE-627 |
005 |
20250206092131.0 |
007 |
tu |
008 |
231223s2005 xx ||||| 00| ||eng c |
028 |
5 |
2 |
|a pubmed25n0517.xml
|
035 |
|
|
|a (DE-627)NLM155173553
|
035 |
|
|
|a (NLM)15870021
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Sutton, Steven A
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a Anti-IL-5 and hypereosinophilic syndromes
|
264 |
|
1 |
|c 2005
|
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 30.06.2005
|
500 |
|
|
|a Date Revised 19.11.2015
|
500 |
|
|
|a published: Print
|
500 |
|
|
|a Citation Status MEDLINE
|
520 |
|
|
|a Hypereosinophilic syndromes represent a heterogeneous group of disorders characterized by peripheral eosinophilia and end-organ damage associated with eosinophil infiltrations. In many instances, the eosinophilia is refractory to standard therapies and clinicians rely on potentially toxic alternatives. This group of disorders has recently gained attention with the description of patients that harbor a genetic rearrangement that produces a constitutively active tyrosine kinase, often responsive to anti-tyrosine kinase therapy. In addition, the recent expansion in our understanding of the mechanisms by which eosinophils develop and become activated, involving the cytokine interleukin-5 (IL-5), has led to advances in therapeutic options. A new therapy currently in clinical trials is the humanized monoclonal antibody against IL-5. This review will discuss the etiology, classification, and treatment options for the hypereosinophilic syndromes, with particular emphasis on anti-interleukin-5 therapy
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a Review
|
650 |
|
7 |
|a Antibodies, Monoclonal
|2 NLM
|
650 |
|
7 |
|a Benzamides
|2 NLM
|
650 |
|
7 |
|a Interleukin-5
|2 NLM
|
650 |
|
7 |
|a Piperazines
|2 NLM
|
650 |
|
7 |
|a Protein Kinase Inhibitors
|2 NLM
|
650 |
|
7 |
|a Pyrimidines
|2 NLM
|
650 |
|
7 |
|a Imatinib Mesylate
|2 NLM
|
650 |
|
7 |
|a 8A1O1M485B
|2 NLM
|
700 |
1 |
|
|a Assa'ad, Amal H
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Rothenberg, Marc E
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 115(2005), 1 vom: 01. Apr., Seite 51-60
|w (DE-627)NLM098196855
|x 1521-6616
|7 nnns
|
773 |
1 |
8 |
|g volume:115
|g year:2005
|g number:1
|g day:01
|g month:04
|g pages:51-60
|
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 115
|j 2005
|e 1
|b 01
|c 04
|h 51-60
|