22 research outputs found
The influence of T cell development on pathogen specificity and autoreactivity
T cells orchestrate adaptive immune responses upon activation. T cell
activation requires sufficiently strong binding of T cell receptors on their
surface to short peptides derived from foreign proteins bound to protein
products of the major histocompatibility (MHC) gene products, which are
displayed on the surface of antigen presenting cells. T cells can also interact
with peptide-MHC complexes, where the peptide is derived from host (self)
proteins. A diverse repertoire of relatively self-tolerant T cell receptors is
selected in the thymus. We study a model, computationally and analytically, to
describe how thymic selection shapes the repertoire of T cell receptors, such
that T cell receptor recognition of pathogenic peptides is both specific and
degenerate. We also discuss the escape probability of autoimmune T cells from
the thymus.Comment: 12 pages, 7 figure
Fungal infection control by garlic extracts (Allium sativum L.) and modulation of peritoneal macrophages activity in murine model of sporotrichosis
Sunitinib treatment in pediatric patients with advanced GIST following failure of imatinib
Background. Sunitinib inhibits KIT and other members of the split-kinase-domain family of receptor tyrosine kinases. Sunitinib prolongs survival in adult patients with imatinib-resistant gastrointestinal stromal tumor (GIST). We report the experience with sunitinib in pediatric patients with advanced GIST following failure of imatinib. Procedure. Sunitinib therapy was provided through a treatment-use protocol. Patients were 10-17 years old at enrollment. All patients had GIST resistant to imatinib therapy. Sunitinib was administered daily for 4 weeks in 6-week treatment cycles. KIT and platelet-derived growth factor receptor alpha (PDGFRA) genotyping of tumor tissue were performed. Results. One patient achieved a partial response, five patients had stable disease and one patient had progressive disease on sunitinib. The duration of disease stabilization was between 7 and 21+ months, with a mean of 15 months. Time to tumor progression was longer on sunitinib than on prior imatinib treatment for five of six patients. Two patients experienced grade 3 adverse events. All other adverse events were grade 1-2. None of the five patients tested had mutations in KIT or PDGFRA. Conclusion. Sunitinib treatment was associated with substantial initial antitumor activity and acceptable tolerability in this group of pediatric patients with imatinib-resistant GIST