Inactivated pepsin inhibits neutrophil activation by Fcgamma-receptor-dependent and independent stimuli

Copyright © 2016 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 169(2016) vom: 01. Aug., Seite 85-88
Auteur principal: Kustiawan, Iwan (Auteur)
Autres auteurs: Derksen, Ninotska, Rispens, Theo
Format: Article en ligne
Langue:English
Publié: 2016
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Immunomodulation Intravenous immunoglobulin (IVIg) Neutrophil Pepsin FCGR1A protein, human Immunoglobulin Fab Fragments Immunoglobulin G Immunoglobulins, Intravenous Receptors, IgG plus... Cytochalasin B 3CHI920QS7 N-Formylmethionine Leucyl-Phenylalanine 59880-97-6 Leukocyte Elastase EC 3.4.21.37 Pepsin A EC 3.4.23.1
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245 1 0 |a Inactivated pepsin inhibits neutrophil activation by Fcgamma-receptor-dependent and independent stimuli 
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520 |a Pepsin is widely used to produce F(ab')2 fragments of immunoglobulin G (IgG). In many cases, at least part of the pepsin will remain present in the F(ab')2 preparation, albeit in (irreversibly) inactivated form. Here we report on a potent immunomodulatory effect of irreversibly inactivated pepsin on activated human neutrophils. Degranulation, induced by coated IgG or via cytochalasin B/N-formyl-Met-Leu-Phe, was measured by quantifying elastase release, and was found to be inhibited in a dose-dependent manner by inactivated pepsin. Since a number of intravenous immunoglobulin (IVIg) products are also treated by limited digestion with pepsin, we investigated if pepsin would be present in quantities large enough to inhibit neutrophil activation. The amounts of pepsin detected in three different pepsin-treated IVIg products were found to be too low to induce an effect, at least in an in vitro setting 
650 4 |a Journal Article 
650 4 |a Immunomodulation 
650 4 |a Intravenous immunoglobulin (IVIg) 
650 4 |a Neutrophil 
650 4 |a Pepsin 
650 7 |a FCGR1A protein, human  |2 NLM 
650 7 |a Immunoglobulin Fab Fragments  |2 NLM 
650 7 |a Immunoglobulin G  |2 NLM 
650 7 |a Immunoglobulins, Intravenous  |2 NLM 
650 7 |a Receptors, IgG  |2 NLM 
650 7 |a Cytochalasin B  |2 NLM 
650 7 |a 3CHI920QS7  |2 NLM 
650 7 |a N-Formylmethionine Leucyl-Phenylalanine  |2 NLM 
650 7 |a 59880-97-6  |2 NLM 
650 7 |a Leukocyte Elastase  |2 NLM 
650 7 |a EC 3.4.21.37  |2 NLM 
650 7 |a Pepsin A  |2 NLM 
650 7 |a EC 3.4.23.1  |2 NLM 
700 1 |a Derksen, Ninotska  |e verfasserin  |4 aut 
700 1 |a Rispens, Theo  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Clinical immunology (Orlando, Fla.)  |d 1999  |g 169(2016) vom: 01. Aug., Seite 85-88  |w (DE-627)NLM098196855  |x 1521-7035  |7 nnns 
773 1 8 |g volume:169  |g year:2016  |g day:01  |g month:08  |g pages:85-88 
856 4 0 |u http://dx.doi.org/10.1016/j.clim.2016.06.008  |3 Volltext 
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952 |d 169  |j 2016  |b 01  |c 08  |h 85-88