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Hashimoto's thyroiditis (HT) is an organ-specific immune disease characterized by the presence of lymphocytic infiltration and serum autoantibodies. Previous studies have confirmed the critical role of Th17 cells in the pathopoiesis of HT patients. Additionally, regulatory T cells (Treg) display a dysregulatory function in autoimmune disease. The purpose of this study is to investigate the alteration of Th17 and Treg cells in HT patients and explore contributing factors. We found there was an increased ratio of Th17/Treg in HT patients and a positive correlation with autoantibodies (anti-TgAb). In addition, there was an increased level of GITRL, which has been demonstrated to be correlated with the increassement of Th17 cells in the serum and thyroid glands of HT patients; the upregulated serum level of GITRL has a positive correlation with the percentage of Th17 cells in HT patients. In summary, an increase in GITRL may impair the balance of Th17/Treg, and contribute to the pathopoiesis of Hashimoto's thyroiditis. [ABSTRACT FROM AUTHOR]

Various polysaccharides purified from plants are considered to be biological response modifiers and have been shown to enhance immune responses. Ficus carica L. is a Chinese traditional plant and has been widely used in Asian countries for its anti-tumor properties. Ficus carica polysaccharides (FCPS), one of the most essential and effective components in Ficus carica L., have been considered to be a beneficial immunomodulator and may be used in immunotherapy. However, the immunologic mechanism of FCPS is still unclear. Dectin-1 is a non-toll-like pattern recognition receptor, predominately expressed on dendritic cells (DCs). Activation of DCs through dectin-1 signaling can lead to the maturation of DC, thus inducing both innate and adaptive immune responses against tumor development and microbial infection. In our study, we found that FCPS could effectively stimulate DCs, partially through the dectin-1/Syk pathway, and promote their maturation, as shown by the up-regulation of CD40, CD80, CD86, and major histocompatibility complex II (MHCII). FCPS also enhanced the production of cytokines by DCs, including IL-12, IFN-γ, IL-6, and IL-23. Moreover, FCPS-treated DCs showed an enhanced capability to stimulate T cells and promote T cell proliferation. Altogether, these results demonstrate that FCPS are able to activate and maturate DCs, thereby up-regulating the immunostimulatory capacity of DCs, which leads to enhanced T cell responses. [ABSTRACT FROM AUTHOR]

Background: β-Glucans have been shown to function as a potent immunomodulator to stimulate innate and adaptive immune responses, which contributes to their anti-tumor property. However, their mechanisms of action are still elusive. Glucocorticoid-induced TNF receptor ligand (GITRL), a member of the TNF superfamily, binds to its receptor, GITR, on both effector and regulatory T cells, generates a positive co-stimulatory signal implicated in a wide range of T cell functions, which is important for the development of immune responses. Methodology/Principal Findings: In this study, we found that whole β-glucan particles (WGPs) could activate dendritic cells (DCs) via dectin-1 receptor, and increase the expression of GITRL on DCs in vitro and in vivo. Furthermore, we demonstrated that the increased GITRL on DCs could impair the regulartory T cell (Treg)-mediated suppression and enhance effector T cell proliferation in a GITR/GITRL dependent way. In tumor models, DCs with high levels of GITRL were of great potential to prime cytotoxic T lymphocyte (CTL) responses and down-regulate the suppressive activity of Treg cells, thereby leading to the delayed tumor progression. Conclusions/Significance: These findings suggest that particulate β-glucans can be used as an immunomodulator to stimulate potent T cell-mediated adaptive immunity while down-regulate suppressive immune activity via GITR/GITRL interaction, leading to a more efficient defense mechanism against tumor development. [ABSTRACT FROM AUTHOR]

Soil organic carbon (SOC) accumulation is strongly affected by soil erosion and deposition that differ at slope positions of a watershed. However, studies on the effects of topography on soil aggregation and SOC dynamics, especially after the implementation of vegetation restoration, are rare. Poorly understood mechanisms and a lack of quantification for the suite of ecological benefits brought by the impacts of topography after planting further obstructed our understanding of terrestrial ecosystem carbon (C) sequestration. The purposes of this study are to (1) quantify the impacts of vegetation restoration on size and stability of soil aggregates and the sequestration of C in soil and (2) to address the impacts of various slope locations on aggregates and SOC distribution. The experimental sites were set up in 1959 on a highly disturbed barren land in a tropical and coastal area of Guangdong province in South China. One site received human-induced vegetation restoration (the restored site), while the other received no planting and has remained as barren land (the barren site). The soil in the study sites was a latosol developed from granite. Soil samples were taken from 0 to 20 and 20 to 40 cm soil layer at shoulder and toe slope positions at both sites for comparisons. Soils were analyzed for proportion of soil macroaggregates (>0.25 mm), the SOC in soil layers, and the aggregate soil organic carbon (AOC) at different aggregate sizes. Measurements in 2007 showed that fractions of water stable macroaggregates in 0–40 cm at shoulder and toe slope ranged from 28% to 45%, about one third to one half of those of dry macroaggregates (91–95%) at the restored site. Soil macroaggregates were not detected at barren site in 2007. Average SOC storage in 0–40 cm soil layer of shoulder and toe slope positions at the restored site was 56.5 ± 10.9 Mg C ha−1, about 2.4 times of that (23.4 ± 4.6 Mg C ha−1) at barren site in 2007. Since 1959, the soil aggregation and SOC storage are significantly improved at the restored site; opposite to that, soil physical and chemical quality has remained low on the barren land without planting. SOC storage in 0–40 cm at toe slope was 15.9 ± 1.8 Mg C ha−1, which is only half of that (30.9 ± 9 Mg C ha−1) at shoulder slope of the barren site; this is opposite to the pattern found at restored site. The ratios of AOC in 0–20 cm to AOC in 20–40 cm at toe slope were lower than those at shoulder slope of the restored site. The comparison of organic carbon sequestered in soils at different slope positions suggest that soil aggregates played a role in sequestering C based upon landscape positions and soil profile depth as a consequence of soil erosion and deposition. Results indicate that vegetation restoration and SOC accumulation significantly enhance soil aggregation, which in turn promotes further organic C accumulation in the aggregates via physical protection. Soil aggregation and soil C accumulation differed between slope positions. Soil aggregation was significantly enhanced in 0–20 cm layer and aggregates absorb C into deep layers in depositional environment (toe slope) under protection from human disturbances. The interactions of erosion–deposition, soil aggregates, and vegetation restoration play important roles on SOC accumulation and redistribution on land. The positive feedback between SOC and soil aggregates should be evaluated for improving the quantification of the impacts of land use change, erosion, and deposition on the dynamics of SOC and soil structure under the global climate change. [ABSTRACT FROM AUTHOR]

To quantify the consequences of erosion and vegetation restoration on ecosystem C dynamics (a key element in understanding the terrestrial C cycle), field measurements were collected since 1959 at two experimental sites set upon highly disturbed barren land in South China. One site had received vegetation restoration (the restored site) while the other received no planting and remained barren (the barren Site). The Erosion-Deposition Carbon Model (EDCM) was used to simulate the ecosystem C dynamics at both sites. The on-site observations in 2007 showed that soil organic C (SOC) storage in the top 80-cm soil layer at the barren site was 50.3 ± 3.5 Mg C ha-1, half that of the restored site. The SOC and surface soil loss by erosion at the restored site from 1959 to 2007 was 3.7 Mg C ha-1 and 2.2 cm, respectively - one-third and one-eighth that of the barren site. The on-site C sequestration in SOC and vegetation at the restored site was 0.67 and 2.5 Mg C ha-1 yr-1, respectively, from 1959 to 2007, driven largely by tree growth and high atmospheric N deposition in the study area. Simulated findings suggested that higher N deposition resulted in higher on-site SOC storage in the soil profile (with SOC in the top 20-cm layer increasing more significantly), and higher on-site ecosystem C sequestration as long as N saturation was not reached. Lacking human-induced vegetation recovery, the barren site remained as barren land from 1959 to 2007 and the on-site C decrease was 0.28 Mg C ha-1 yr-1. Our study clearly indicated that vegetation restoration and burial by soil erosion provide a large potential C sink in terrestrial ecosystems. [ABSTRACT FROM AUTHOR]

Studies the mechanical properties, water swelling behavior and morphology of swellable rubber compatibilized by polyvinyl alcohol-g-polybutylacrylate (PVA-g-PBA). Preparation of a novel water swellable rubber; Incorporation of amphiphilic graft copolymer PVA-g-PBA as the compatibilizer between chlorohydrin rubber and crosslinked polyacrylate; Improvement of water swelling behavior.

Background: Hepatitis B infections, characterized by the presence of a viral genome without detectable hepatitis B surface antigen (HBsAg; Occult hepatitis B infection [OBI]), have been reported recently. Objectives: We performed serological and molecular characterization of OBI among blood donors at Jiangsu province blood center during years 2013 and 2014. Methods: All donor samples were routinely screened by double enzyme-linked immunosorbent assay (ELISA) for hepatitis C virus (HCV), hepatitis B virus (HBV), human immunodeficiency virus (HIV), Treponema pallidum (TP), and alanine aminotransferase (ALT). Single-reactive, nonreactive, and ALT-elevated samples were pooled or resolved by nucleic acid testing (NAT). Seromarkers were examined in HBsAg-/DNA+ samples. After 1 to 12 months of follow up, seromarkers were screened again to verify OBI samples. Results:We studied 157119 samples from blood donors. A total of 154397 ELISA nonreactive donor samples were identified, andHBVDNAwas detected in 81 samples; no samples were positive for HIV or HCV RNA. Hepatitis B virus viral loads in most donors were less than 20 - 200 IU/mL. There was only one HBsAg-positive sample. Eighty HBsAg-/DNA+ samples were evaluated further. Of these samples, 85% (68/80) were reactive for anti-HBc and 36.2% (29/800) were reactive for anti-HBc and anti-HBs; 11.3% (9/80) did not have any detectable serological markers. Twenty-nine donors were followed up. One was HBsAg ELISA positive, and of six seronegative donors, all had anti-HBc and anti-HBs, but were negative for DNA. Samples were HBV genotypes B, C and D. Mutations in the S region of HBV DNA included S114T, G119R, P120S, T125M, C139Y, T140I, C147W, T148A, A159V/G, E164D, V168A, and R169C. Conclusions: Overall, we found that OBI was rare, but that the prevalence of OBI was slightly higher in Jiangsu than in other areas of China. [ABSTRACT FROM AUTHOR]

Myeloid-derived suppressor cells (MDSCs) play a critical role in tumor-associated immunosuppression, thus affecting effective immunotherapies for cancers. However, the molecular mechanisms involved in regulating the differentiation and function of MDSCs remain largely unclear. In this study, we found that inhibition of microRNA (miR)-9 promoted the differentiation of MDSCs with significantly reduced immunosuppressive function whereas overexpression of miR-9 markedly enhanced the function of MDSCs. Notably, knockdown of miR-9 significantly impaired the activity of MDSCs and inhibited the tumor growth of Lewis lung carcinoma in mice. Moreover, miR-9 regulated MDSCs differentiation by targeting the runt-related transcription factor 1, an essential transcription factor in regulating MDSC differentiation and function. Furthermore, the CREB was found to regulate miR-9 expression in MDSCs. Taken together, our findings have identified a critical role of miR-9 in regulating the differentiation and function of MDSCs. [ABSTRACT FROM AUTHOR]