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Efficient antigen presentation of soluble, but not particulate, antigen in the absence of Wiskott–Aldrich syndrome protein
Author(s) -
Westerberg Lisa,
Wallin Robert P. A.,
Greicius Gediminas,
Ljunggren HansGustaf,
Severinson Eva
Publication year - 2003
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1046/j.1365-2567.2003.01668.x
Subject(s) - antigen presentation , antigen , wiskott–aldrich syndrome protein , antigen presenting cell , biology , ovalbumin , immune system , cd40 , dendritic cell , antigen processing , microbiology and biotechnology , immunology , t cell , cytotoxic t cell , in vitro , cell , biochemistry , actin cytoskeleton , cytoskeleton
Summary B cells and dendritic cells, lacking functional Wiskott–Aldrich syndrome protein (WASP), have aberrant formation of membrane protrusions. We hypothesized that protrusions may play a role in antigen presentation, and consequently, that impaired antigen presentation may be an underlying factor of the immune deficiency in patients with Wiskott–Aldrich syndrome. In this paper, we investigated the antigen presentation capacity of B cells and dendritic cells from WASP knockout mice, using soluble and particulate antigen, to CD4 + T cells from T‐cell receptor transgenic DO11.10 mice. As antigen we used soluble ovalbumin (OVA), a peptide thereof (amino acids 323–339) or bacteria expressing OVA. We found that WASP‐deficient B cells and dendritic cells efficiently processed and presented soluble OVA protein as well as its peptide in vitro , inducing proliferation and cytokine production from CD4 + T cells. Antigen presentation of soluble protein was efficient also in vivo , because immunization of WASP‐deficient mice with OVA elicited proliferation of transferred, fluorescent‐labelled, CD4 + T cells. Although we could detect uptake of bacteria in dendritic cells, processing and presentation of bacterial‐expressed OVA was impaired in WASP‐deficient dendritic cells. In conclusion, our data suggest that WASP is not needed for processing and presentation of soluble antigen, but that efficient presentation of particulate antigen require WASP.