التفاصيل البيبلوغرافية
| العنوان: |
The expression of legumain, an asparaginyl endopeptidase that controls antigen processing, is reduced in endotoxin-tolerant monocytes. |
| المؤلفون: |
Wolk, K.1, Grütz, G.1, Witte, K.1, Volk, H.-D.1, Sabat, R.1 robert.sabat@charite.de |
| المصدر: |
Genes & Immunity. Aug2005, Vol. 6 Issue 5, p452-456. 5p. |
| مصطلحات موضوعية: |
*MONOCYTES, *ENDOTOXINS, *ENDOPEPTIDASES, *ANTIGENS, *B cells |
| مستخلص: |
The exposition of monocytes to lipopolysaccharide (LPS) primarily causes a massive inflammatory response that is then followed by a hyporesponsive state of these cells. This latter state is called endotoxin tolerance and is characterized by (i) the attenuated production of proinflammatory mediators after repeated LPS treatment, and (ii) the diminished antigen presentation and T-cell stimulation capacity. The data presented here indicate that LPS priming causes a specific decrease in the expression of legumain (the asparaginyl endopeptidase responsible for the key step in antigen processing) in monocytes. In these cells, the fraction of major histocompatibility complex (MHC) class II loaded with CLIP was increased. In contrast to monocytes, LPS priming provoked an increase of legumain expression in B cells. Reduced monocytic expression of legumain was also found in critically ill patients supporting the suitability of endotoxin tolerance as an experimental model of clinical postinflammatory immunodeficiency.Genes and Immunity (2005) 6, 452–456. doi:10.1038/sj.gene.6364224; published online 5 May 2005 [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
Academic Search Index |
Full Text Finder