conclusions the cd4+ and cd8+ tcr vβ gene families undergo clonal expansion in cshb patients, and cd8+ t cells play a major role in the pathogenesis of cshb. moreover, the conserved motifs and limited use of joining region genes observed in the cshb patients of this cohort indicated that similar antigenic epitopes are recognized. results the number of oligoclonal or monoclonal expansion tcr vβ ...

The developmental pathways of long-lived memory CD8 T cells and the lineage relationship between memory T cell subsets remain controversial. Although some studies indicate the two major memory T cell subsets, central memory T (T(CM)) and effector memory T (T(EM)), are related lineages, others suggest that these subsets arise and are maintained independently of one another. In this study, we hav...

It is not known whether subsets of dendritic cells provide diVerent cytokine microenvironments that determine the diVerentiation of either type-1 T helper (TH1) or TH2 cells. Human monocyte (pDC1)-derived dendritic cells (DC1) were found to induce TH1 diVerentiation, whereas dendritic cells (DC2) derived from CD4+CD3−CD11c− plasmacytoid cells (pDC2) induced TH2 diVerentiation by use of a mechan...

CD4+ T cells are principal targets for human immunodeficiency virus type 1 (HIV-1) infection. CD4+ T cell subsets are heterogeneous cell populations, divided by functional and phenotypic differences into naïve and memory T cells. The memory CD4+ T cells are further segregated into central, effector and transitional memory cell subsets by functional, phenotypic and homeostatic characteristics. D...

Differentiation of naïve CD4⁺ cells into functionally distinct effector helper T cell subsets, characterised by distinct "cytokine signatures," is a cardinal strategy employed by the mammalian immune system to efficiently deal with the rapidly evolving array of pathogenic microorganisms encountered by the host. Since the T(H)1/T(H)2 paradigm was first described by Mosmann and Coffman, research ...

Belatacept blocks CD28-mediated T-cell costimulation and prevents renal transplant rejection. Understanding T-cell subset sensitivity to belatacept may identify cellular markers for immunosuppression failure to better guide treatment selection. Here, we evaluate the belatacept sensitivity of allo-antigen-specific CD154-expressing-T-cells, whose T-cytotoxic memory (TcM) subset predicts rejection...