Splenic CD8(+) T cells secrete TGF-beta 1 to exert suppression in mice with anterior chamber-associated immune deviation

Background CD8(+) regulatory T cells (Treg) have been considered to be involved in a model of ocular-induced tolerance, known as anterior chamber-associated immune deviation (ACAID). The mechanisms of suppression by CD8(+) T cells in ACAID remain only poorly understood. TGF-beta 1 is considered as an inhibitory cytokine for immunosuppression in some models. The production of TGF-beta 1 by CD8(+) T cells in ACAID, and whether CD8+ T cells exert suppression through TGF-beta 1, is unknown. Methods The suppressive effect of CD8(+) T cells in ACAID mice was determined by a local adoptive transfer (LAT) assay. The production of TGF-beta 1 by CD8(+) T cells was measured by enzyme-linked immunosorbent assay (ELISA). Anti-TGF-beta 1 antibodies were used in the LAT assay to test if they could block the inhibitory effect of CD8(+) T cells. Results CD8(+) T cells from ACAID mice were shown to block the delayed-type hypersensitivity (DTH) response in an antigen-specific manner in a LAT assay. These CD8+ T cells secreted TGF-beta 1, and their suppression could partially be blocked by anti-TGF-beta 1 antibodies. Conclusions Our study confirms that CD8+ T cells from ACAID mice possess inhibitory properties. This population exerts part of its suppressive function via the production of TGF-beta 1

Local Uniqueness and Convergence of Iterative Methods for Nonsmooth Variational Inequalities

AbstractIn this paper, we study nonsmooth variational inequalities. Using nonsmooth analysis, we characterize various monotonicity properties of locally Lipschitzian functions and give some sufficient conditions to guarantee the local uniqueness of solutions to variational inequalities. Two iterative algorithms are also presented to solve nonsmooth variational inequalities

Early subretinal allograft rejection is characterized by innate immune activity

Successful subretinal transplantation is limited by considerable early graft loss, despite pharmacological suppression of adaptive immunity. We postulated that early innate immune activity is a dominant factor in determining graft survival and chose a non-immunosuppressed mouse model of retinal pigment epithelial (RPE) cell transplantation to explore this. Expression of almost all measured cytokines by DH01 RPE cells increased significantly following graft preparation and the neutrophil chemoattractant, KC/GRO/CINC, was most significantly increased. Subretinal allografts of DH01 cells (C57BL/10 origin) into healthy, non-immunosuppressed C57BL/6 murine eyes were harvested and fixed at 1, 3, 7 and 28 days post-operatively and subsequently cryosectioned and stained. Graft cells were detected using SV40 large T antigen (SV40T) immunolabeling and apoptosis/necrosis by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL). Sections were also immunolabeled for macrophage (CD11b & F4/80), neutrophil (Gr1 Ly-6G), and T-lymphocyte (CD3-ε) infiltration. Images captured with an Olympus FV1000 confocal microscope were analyzed using Imaris software. The proportion of the subretinal bolus comprising graft cells (SV40T+) was significantly (p<0.001) reduced between post-operative day (POD) 3 (90% ± 4%) and POD 7 (20% ± 7%). CD11b+, F4/80+ and Gr1 Ly-6G+ cells increased significantly (p<0.05) from POD 1 and predominated over SV40T+ cells by POD 7. Co-labeling confocal microscopic analysis demonstrated graft engulfment by neutrophils and macrophages at POD 7 and reconstruction of z-stacked confocal images confirmed SV40T inside Gr1 Ly-6G+ cells. Expression of CD3-ε was low and did not differ significantly between time-points. By POD 28, no graft cells were detectable and few inflammatory cells remained. These studies reveal for the first time a critical role for innate immune mechanisms early in subretinal graft rejection. The future success of subretinal transplantation will require more emphasis on techniques to limit innate immune-mediated graft loss, rather than focusing exclusively on suppression of the adaptive immune response

Evaluation of hardening behavior under synergistic interaction of He and subsequent H ions irradiation in vanadium alloys

Helium and hydrogen synergy effect on irradiation hardening in V-4Cr-4Ti alloys was investigated. The samples were irradiated helium or helium + hydrogen ions at RT (room temperature) and 300 °C. Transmission electron microscopy (TEM) and nano-indentation test were used to investigate the defects and hardness evolution induced by ion irradiation, respectively. The curves for irradiation induced hardness have been analyzed by indentation size effect (ISE) and soft substrate effect (SSE) on the basis of Nix-Gao model and Kasada's method. Point defects appeared after irradiation at RT and dislocation loops and bubbles observed after irradiation at 300 °C were responsible for hardening. The hardness after He + H ions irradiation at RT increased comparison with that of He irradiation samples at RT and 300 °C because the synergistic interaction of pre-implanted He, subsequent H and the irradiation-induced defects may affect the evolution of hardening. Bulk hardness could be evaluated by least square method. Besides ISE, SSE was observed in sample after irradiated He + H at 300 °C. Keywords: Ion irradiation, Defect, Dislocation loop, Bubble, Irradiation hardenin