Document Detail


Invariant NKT cells modulate the suppressive activity of IL-10-secreting neutrophils differentiated with serum amyloid A.
MedLine Citation:
PMID:  20890286     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Neutrophils are the main effector cells during inflammation, but they can also control excessive inflammatory responses by secreting anti-inflammatory cytokines. However, the mechanisms that modulate their plasticity remain unclear. We now show that systemic serum amyloid A 1 (SAA-1) controls the plasticity of neutrophil differentiation. SAA-1 not only induced anti-inflammatory interleukin 10 (IL-10)-secreting neutrophils but also promoted the interaction of invariant natural killer T cells (iNKT cells) with those neutrophils, a process that limited their suppressive activity by diminishing the production of IL-10 and enhancing the production of IL-12. Because SAA-1-producing melanomas promoted differentiation of IL-10-secreting neutrophils, harnessing iNKT cells could be useful therapeutically by decreasing the frequency of immunosuppressive neutrophils and restoring tumor-specific immune responses.
Authors:
Carmela De Santo; Ramon Arscott; Sarah Booth; Ioannis Karydis; Margaret Jones; Ruth Asher; Mariolina Salio; Mark Middleton; Vincenzo Cerundolo
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-10-03
Journal Detail:
Title:  Nature immunology     Volume:  11     ISSN:  1529-2916     ISO Abbreviation:  Nat. Immunol.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-10-20     Completed Date:  2010-11-23     Revised Date:  2011-11-28    
Medline Journal Info:
Nlm Unique ID:  100941354     Medline TA:  Nat Immunol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1039-46     Citation Subset:  IM    
Affiliation:
Medical Research Council Human Immunology Unit, Nuffield Department of Medicine, Medical Research Council Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Differentiation / immunology*
Cell Line, Tumor
Female
Humans
Interleukin-10 / immunology*
Melanoma / immunology*
Mice
Mice, Inbred C57BL
Natural Killer T-Cells / immunology*
Neutrophils / cytology,  immunology*
Serum Amyloid A Protein / immunology*
Grant Support
ID/Acronym/Agency:
084923/Z/08/Z//Wellcome Trust; A11331//Cancer Research UK; A6199//Cancer Research UK; C399/A2291//Cancer Research UK; //Medical Research Council
Chemical
Reg. No./Substance:
0/Serum Amyloid A Protein; 130068-27-8/Interleukin-10
Comments/Corrections
Comment In:
Nat Immunol. 2011 Nov;12(11):1017-8; author reply 1018-20   [PMID:  22012430 ]
Nat Immunol. 2010 Nov;11(11):981-2   [PMID:  20959800 ]
Nat Rev Immunol. 2010 Nov;10(11):752   [PMID:  21080614 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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