For example, analysis of TREC content in different subpopulations of mucosal lymphocytes would probably shed more light on the immunopathogenesis of IBD. The current method chosen for TREC analysis is limited to show whether the TREC levels are increased or decreased in IBD patients, and do not show the actual frequency of TREC-positive T cells in the population. Recently, several mathematical models have been developed to determine thymic output, with equations that consider parameters that influence directly the measurement of TRECs (cell death, proliferation, age, etc.). It would thus be of great interest

RO4929097 to apply mathematical modelling for analysis of RTE in patients with IBD and also other inflammatory conditions in comparison to uninflamed controls. Such studies are currently under way in our research LEE011 group using the Gαi2-deficient mouse model of colitis. This study was supported by grants from the Swedish Research Council Medicine and Health, the Swedish Cancer Society, Nanna Svartz Foundation, the

Health and Medical Care Committee of Regional Executive Board Region Västra Götaland (LUA-ALF) and the Bengt Ihre’s foundation. The authors thank Dr Solveig Oskarsdottir, Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska University Hospital, Göteborg, for providing thymic tissue samples from human infants. The authors declare no conflicts of interest. “
“The spleen is the main organ for immune defense during infection Ergoloid with Plasmodium parasites and splenomegaly is one of the major symptoms of such infections. Using a rodent model of Plasmodium yoelii infection, MHC class II+CD11c− non-T, non-B cells in the spleen were characterized. Although the proportion of conventional dendritic cells was reduced, that of MHC II+CD11c− non-T, non-B cells increased during the course of infection. The increase in this subpopulation was dependent on the presence of lymphocytes. Experiments using Rag-2−/− mice with adoptively transferred normal spleen cells indicated that these cells were non-lymphoid cells;

however, their accumulation in the spleen during infection with P. yoelii depended on lymphocytes. Functionally, these MHC II+CD11c− non-T, non-B cells were able to produce the proinflammatory cytokines alpha tumor necrosis factor and interleukin-6 in response to infected red blood cells, but had only a limited ability to activate antigen-specific CD4+ T cells. This study revealed a novel interaction between MHC II+CD11c− non-lymphoid cells and lymphoid cells in the accumulations of these non-lymphoid cells in the spleen during infection with P. yoelii. Protective immune responses against the blood stage of malarial infection require antibody and CD4+ T cell immune responses [1]. Presentation of antigens to T cells by APCs initiates activation of adaptive immunity.