Owing to the ability of TCRs above an affinity threshold level to recognize self-protein, caution must be observed, and it is therefore necessary for all TCRs that have an increased affinity to undergo extensive in vitro and in vivo screening before reaching the clinical setting. This review has described areas of basic T-cell immunology of fundamental

importance to the field of TCR gene transfer and T-cell immunotherapy. However, the ability to transfer TCRs of known affinity and specificity into human or murine T cells ‘at will’ can facilitate further studies into the critical steps of TCR pairing and assembly, antigen recognition, T-cell signalling and function of self-reactive T cells, amongst others. Current research is focused RXDX-106 in vitro on improving the function of TCR-transduced T cells, but also on exploring selleck chemicals the introduction of TCR-αβ chains into alternative T-cell subsets, such as CD4+ helper T cells,7 CD4+ CD25+ regulatory T cells47,48 and γδ T cells,29 to generate specialized antigen-specific T cells. EM and HS are members of the Scientific Advisory Board of CellMedica Ltd. “
“Genetically altered mice carrying mutations of genes encoding crucial components of the immune system and lipid metabolism have been widely used to study the role of immune responses and inflammation in atherosclerosis.

These mice are often fed a diet, with a high content of cholesterol and saturated fat in order to induce hypercholesterolemia and arterial lesions. We review the different mouse models of atherosclerosis, type of diets, and techniques to measure lipid deposition and lesion size in the arterial walls. Moreover, the methods used to determine the presence of the immune cells in atherosclerotic lesions are also described here. Curr. Protoc.

Immunol. 96:15.24.1-15.24.23. © 2012 by John Wiley & Sons, Inc. “
“Over the past 10 years we have made great strides in ALOX15 our understanding of T helper cell differentiation, expansion and effector functions. Within the context of T helper type 2 (Th2) cell development, novel innate-like cells with the capacity to secrete large amounts of interleukin-5 (IL-5), IL-13 and IL-9 as well as IL-4-producing and antigen-processing basophils have (re)-emerged onto the type 2 scene. To what extent these new players influence αβ+ CD4+ Th2 cell differentiation is discussed throughout this appraisal of the current literature. We highlight the unique features of Th2 cell development, highlighting the three necessary signals, T-cell receptor ligation, co-stimulation and cytokine receptor ligation. Finally, putting these into context, microbial and allergenic properties that trigger Th2 cell differentiation and how these influence Th2 effector function are discussed and questioned.