Article

Neutrophils influence the level of antigen presentation during the immune response to protein antigens in adjuvants.

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
The Journal of Immunology (impact factor: 5.79). 09/2010; 185(5):2927-34. DOI:10.4049/jimmunol.1001289 pp.2927-34
Source: PubMed

ABSTRACT Neutrophils modulated Ag presentation following immunization with Ags in CFA or IFA or alum. The neutrophils had an important negative role in the CD4 T cell and B cell responses to three protein Ags: hen egg white lysozyme, OVA, and listeriolysin O. In their absence (by depleting with Abs for only the first 24 h, or using genetically neutropenic mice), the cellular responses increased several-fold. The CD8 response was not affected or slightly decreased. Competition for Ag between the presenting cells and the neutrophils, as well as an effect on the response to Ag-bearing dendritic cells (DCs), was documented. Neutrophils entered the draining lymph nodes rapidly and for a brief period of several hours, localizing mainly to the marginal sinus and superficial cortex. There they established brief contact with DCs and macrophages. Moreover, neutrophils imprinted on the quality of the subsequent DC-T cell interactions, despite no physical contact with them; by intravital microscopy, the clustering of Ag-specific T cells and DCs was improved in neutropenic mice. Thus, neutrophils are obligate cells that briefly enter sites of immunization and set the level of Ag presentation. A brief depletion may have a considerably positive impact on vaccination.

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Keywords

Ag presentation
 
Ag-bearing dendritic cells
 
Ag-specific T cells
 
B cell responses
 
brief contact
 
brief period
 
CD4 T cell
 
draining lymph nodes
 
first 24 h
 
genetically neutropenic mice
 
hen egg white lysozyme
 
intravital microscopy
 
listeriolysin O
 
negative role
 
neutropenic mice
 
neutrophils imprinted
 
Neutrophils modulated Ag presentation
 
physical contact
 
protein Ags
 
subsequent DC-T cell interactions