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The stress of parturition in the dairy cow is associated with increased susceptibility to infectious disease. During the periparturient period the demands for calcium are increased; these increased demands for calcium can result in subclinical or clinical hypocalcemia. Periparturient cows also experience significant immune suppression. Because intracellular calcium signaling is a key early feature in immune cell activation, we have hypothesized that the increased demand for calcium in periparturient cows may adversely affect intracellular calcium stores of immune cells. This reduction in intracellular calcium stores in immune cells could blunt intracellular calcium release following an activating stimulus, contributing to the immune suppression seen in these animals. To test this hypothesis, peripheral mononuclear cells were obtained from 27 multiparous dairy cows spanning a period of 2 wk before and 2 wk after parturition. Following activation of these cells by anti-CD3 antibodies plus secondary antibodies, intracellular calcium release from intracellular stores was measured. The intracellular calcium released in response to the activation signal declined as calcium demand for lactation became more intense and recovered as plasma calcium normalized. Intracellular calcium stores in peripheral mononuclear cells, estimated by pretreating cells with pervanadate and ionomycin, significantly decreased at parturition and returned to normal levels as the cows’ blood calcium returned to normal levels. Hypocalcemia, which is common in periparturient dairy cows, is associated with decreased intracellular calcium stores in peripheral mononuclear cells. Our data suggest that this is the cause of a blunted intracellular calcium release response to an immune cell activation signal. It is concluded that intracellular Ca stores decrease in peripheral blood mononuclear cells (PBMC) before parturition and development of hypocalcemia. This suggests that systemic calcium stress precedes measurable hypocalcemia, particularly in cows that will develop milk fever. Therefore, PBMC intracellular Ca stores are a more sensitive measure of calcium stresses in transition cow. This decrease in PBMC intracellular Ca stores before parturition and the development of hypocalcemia contributes to periparturient immune suppression. 相似文献
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Ruiyue Yang Xinrong Pei Junbo Wang Zhaofeng Zhang Haifeng Zhao Qiong Li Ming Zhao Yong Li 《Journal of the science of food and agriculture》2010,90(13):2241-2248
BACKGROUND: A marine oligopeptide preparation (MOP) obtained from Chum Salmon (Oncorhynchus keta) by the method of enzymatic hydrolysis, has been found to enhance the innate and adaptive immunities through stimulation of the secretion of cytokines in mice. The current study aimed to further investigate the protective effect of MOP on radiation‐induced immune suppression in mice. RESULTS: Female ICR mice (6–8 weeks old) were randomly divided into three groups, i.e. blank control, irradiation control and MOP (1.350 g kg?1 body weight) plus irradiation‐treated group. MOP significantly increased the survival rate and prolonged the survival times for 30 days after irradiation, and lessened the radiation‐induced suppression of T‐ or B‐lymphocyte proliferation, resulting in the recovery of cell‐mediated and humoral immune functions. This effect may be produced by augmentation of the relative numbers of radioresistant CD4+ T cells, enhancement of the level of immunostimulatory cytokine, IL‐12, reduction of the level of total cellular NF‐κB through the induction of IκB in spleen and inhibition of the apoptosis of splenocytes. CONCLUSION: We propose that MOP be used as an ideal adjuvant therapy to alleviate radiation‐induced injuries in cancer patients. Copyright © 2010 Society of Chemical Industry 相似文献
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Dr. Pradeep K. Singh Hao Fan Xiuju Jiang Prof. Dr. Lei Shi Prof. Dr. Carl F. Nathan Prof. Dr. Gang Lin 《ChemMedChem》2016,11(19):2127-2131
N,C‐capped dipeptides belong to a class of noncovalent proteasome inhibitors. Herein we report that the insertion of a β‐amino acid into N,C‐capped dipeptides markedly decreases their inhibitory potency against human constitutive proteasome β5c, while maintaining potent inhibitory activity against human immunoproteasome β5i, thereby achieving thousands‐fold selectivity for β5i over β5c. Structure–activity relationship studies revealed that β5c does not tolerate the β‐amino acid based dipeptidomimetics as does β5i. In vitro, one such compound was found to inhibit human T cell proliferation. Compounds of this class may have potential as therapeutics for autoimmune and inflammatory diseases with less mechanism‐based cytotoxicity than agents that also inhibit the constitutive proteasome. 相似文献
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Sofía Frigerio Dalia A. Lartey Geert R. DHaens Joep Grootjans 《International journal of molecular sciences》2021,22(23)
Patients with inflammatory bowel disease (IBD) have increased incidence of colorectal cancer (CRC). IBD-associated cancer follows a well-characterized sequence of intestinal epithelial changes, in which genetic mutations and molecular aberrations play a key role. IBD-associated cancer develops against a background of chronic inflammation and pro-inflammatory immune cells, and their products contribute to cancer development and progression. In recent years, the effect of the immunosuppressive microenvironment in cancer development and progression has gained more attention, mainly because of the unprecedented anti-tumor effects of immune checkpoint inhibitors in selected groups of patients. Even though IBD-associated cancer develops in the background of chronic inflammation which is associated with activation of endogenous anti-inflammatory or suppressive mechanisms, the potential role of an immunosuppressive microenvironment in these cancers is largely unknown. In this review, we outline the role of the immune system in promoting cancer development in chronic inflammatory diseases such as IBD, with a specific focus on the anti-inflammatory mechanisms and suppressive immune cells that may play a role in IBD-associated tumorigenesis. 相似文献
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目的:研究白玉菇多糖对免疫抑制型小鼠脾脏、胸腺的免疫调节作用。方法:经超声波辅助热水浸提及Sevage法去蛋白得到白玉菇精多糖(RPHM)。将小鼠随机分为空白对照组、模型对照组、阳性对照组、RPHM低剂量组(30 mg/kg bw/d)、RPHM中剂量组(60 mg/kg bw/d)、RPHM高剂量组(120 mg/kg bw/d),每天同时间段进行灌胃,灌胃15 d,建立环磷酰胺(CPA)免疫抑制型小鼠模型。取小鼠脾脏、胸腺,测定其体重、脏器指数;血清细胞因子、单核-巨噬细胞吞噬能力;外周白细胞、红细胞和血小板计数并观察脾脏、胸腺的形态学。结果:与模型组相比,RPHM中剂量组(60 mg/kg bw/d)、高剂量组(120 mg/kg bw/d)可明显提升免疫抑制型小鼠的毛色、活动情况、身体状况、食欲、体重、脾脏指数和胸腺指数、单核-巨噬细胞吞噬功能、骨髓造血功能等指标;也可在一定程度上提高免疫抑制型小鼠IL-2、IL-12、IFN-γ和TNF-α的水平,并改善IL-6的分泌异常情况;还可明显改善免疫抑制型小鼠脾脏、胸腺的病变,改善结构完整度。结论:RPHM对免疫抑制型小鼠的脾脏和胸腺有明显的免疫调节作用。 相似文献
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建立小鼠免疫低下模型和食物过敏模型,采用ELISA法检测外周血中细胞因子(IL-4、IL-6、IL-10、IL-12、IFN-γ、TGF-β)的变化。结果表明:与空白对照组比较,腹腔注射环磷酰胺所建立免疫低下小鼠胸腺指数和脾脏指数均有显著降低(P≤0.05),且在第3天达到最低;经卵清蛋白致敏小鼠外周血IgE水平极显著升高(P≤0.01)。免疫低下小鼠外周血中IFN-γ(除第3天外)、TGF-β含量(除第3天外)和IFN-γ/IL-4比值均显著降低,而IL-10水平也有下降趋势;除第2天外IL-6水平显著升高,但IL-4水平只在第3天显著性增高,IL-12先是下降随后呈现增多的趋势;食物过敏小鼠的IL-4、IL-6、IL-10和TGF-β水平均有显著性增高,IFN-γ/IL-4比值有显著性下降,而IFN-γ和IL-12没有明显的变化。因此,免疫低下和食物过敏小鼠的Th1/Th2细胞平衡均向Th2细胞偏移,免疫低下对Th1细胞的影响大,食物过敏对Th2细胞的影响更明显。 相似文献
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Shuai Guo;Zongheng Li;Ruilong Zhou;Jie Feng;Lin Huang;Bin Ren;Jiaoyang Zhu;Ya Huang;Guochao Wu;Haobin Cai;Qianqian Zhang;Yushen Ke;Tianwang Guan;Peier Chen;Yikai Xu;Chenggong Yan;Caiwen Ou;Zheyu Shen; 《Small (Weinheim an der Bergstrasse, Germany)》2024,20(29):2309842
Triple negative breast cancer (TNBC) cells have a high demand for oxygen and glucose to fuel their growth and spread, shaping the tumor microenvironment (TME) that can lead to a weakened immune system by hypoxia and increased risk of metastasis. To disrupt this vicious circle and improve cancer therapeutic efficacy, a strategy is proposed with the synergy of ferroptosis, immunosuppression reversal and disulfidptosis. An intelligent nanomedicine GOx-IA@HMON@IO is successfully developed to realize this strategy. The Fe release behaviors indicate the glutathione (GSH)-responsive degradation of HMON. The results of titanium sulfate assay, electron spin resonance (ESR) spectra, 5,5’-Dithiobis-(2-nitrobenzoic acid (DTNB) assay and T1-weighted magnetic resonance imaging (MRI) demonstrate the mechanism of the intelligent iron atom (IA)-based cascade reactions for GOx-IA@HMON@IO, generating robust reactive oxygen species (ROS). The results on cells and mice reinforce the synergistic mechanisms of ferroptosis, immunosuppression reversal and disulfidptosis triggered by the GOx-IA@HMON@IO with the following steps: 1) GSH peroxidase 4 (GPX4) depletion by disulfidptosis; 2) IA-based cascade reactions; 3) tumor hypoxia reversal; 4) immunosuppression reversal; 5) GPX4 depletion by immunotherapy. Based on the synergistic mechanisms of ferroptosis, immunosuppression reversal and disulfidptosis, the intelligent nanomedicine GOx-IA@HMON@IO can be used for MRI-guided tumor therapy with excellent biocompatibility and safety. 相似文献
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Ying He;Yunyuan Nong;Junliang Qin;Linlin Feng;Jinghua Qin;Qianyi Wang;Lijun Deng;Siqi Tang;Meiling Zhang;Xiaofeng Fan;Min Dong;Jinbin Wei;Shihan Pan;Zhiheng Su; 《Journal of the science of food and agriculture》2024,104(12):7143-7158
Oyster polypeptide (OP) is a mixture of oligopeptides extracted from oysters through enzyme lysis, separation, and purification. It is associated with immunomodulatory effects, but the underlying mechanisms are not known. This study therefore combined proton nuclear magnetic resonance (1H-NMR) urinary metabolomics and 16S rRNA gene sequencing of the gut microbiome to determine the immunoprotective mechanisms of OP in rats subjected to cyclophosphamide-induced immunosuppression. 相似文献