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EAE

EAE的相关文献在1992年到2022年内共计72篇,主要集中在神经病学与精神病学、基础医学、内科学 等领域,其中期刊论文62篇、会议论文3篇、专利文献7篇;相关期刊38种,包括中国中医基础医学杂志、中医药信息、国际免疫学杂志等; 相关会议3种,包括中国畜牧兽医学会兽医公共卫生学分会成立大会暨第一次学术研讨会、黑龙江省免疫学会成立十周年学术会议、中国科协第三届青年学术年会等;EAE的相关文献由209位作者贡献,包括张凤蕴、何孔旺、俞正玉等。

EAE—发文量

期刊论文>

论文:62 占比:86.11%

会议论文>

论文:3 占比:4.17%

专利文献>

论文:7 占比:9.72%

总计:72篇

EAE—发文趋势图

EAE

-研究学者

  • 张凤蕴
  • 何孔旺
  • 俞正玉
  • 倪艳秀
  • 刘华
  • 刘颖
  • 叶青
  • 吕立新
  • 周俊明
  • 张雪寒
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 李倩; 高杰; 胡蓉; 李红; 彭丽娟; 苏敏
    • 摘要: 探讨BEZ235通过靶向作用PI3K/AKT/FoxO1治疗实验性自身免疫性脑脊髓炎(EAE)的相关机制。取60只C57BL/6小鼠,用髓鞘少突胶质细胞糖蛋白(MOG35-55)和完全弗氏佐剂(CFA)诱导建立EAE模型。小鼠免疫后分别用PBS或BEZ235(5mg穔g-1/d-1)进行灌胃治疗,随机分为EAE组和治疗组。观察小鼠的临床评分,治疗后取脊髓行H&E和LFB染色,观察小鼠脊髓中炎性细胞浸润及脱髓鞘变化。Western blotting检测IL-17、PI3K/AKT/FoxO1在小鼠脊髓中表达;流式细胞术检测T细胞增殖、活化、凋亡、Tregs、初始T细胞、效应T细胞比例。
    • 姬军风; 袁有才; 王伟卓
    • 摘要: 目的:探究大黄酸对实验性自身免疫性脑脊髓炎(EAE)小鼠模型中炎症因子以及Foxp3转录因子(Foxp3)表达量的影响.方法:通过髓鞘少突胶质细胞糖蛋白35-55(MOG35-55)抗原乳剂免疫C57BL/6小鼠制备EAE模型,实验小鼠随机分为对照组、模型组、给药组1、给药组2、给药组3;免疫当天腹腔注射大黄酸5、10、20 mg/kg,对照组和模型组给予等量的生理盐水,连续给药30 d;观察小鼠的发病率、死亡率,并进行临床评分.分别在免疫后第14、20、30天取各组小鼠脑和脊髓组织,酶联免疫吸附法(ELISA)检测白细胞介素2(IL-2)的水平,蛋白质印迹法(Western blot)测定Foxp3蛋白的含量.结果:给予EAE模型小鼠不同剂量的大黄酸给药组较模型组发病率显著降低(P<0.05);模型组小鼠在第20天、第30天脑和脊髓组织中分泌的IL-2较对照组显著增加(P<0.05),脑组织中Foxp3表达量显著降低(P<0.05);给予不同剂量的大黄酸给药组较模型组可显著降低EAE小鼠脑、脊髓组织中的IL-2水平(P<0.05),上调Foxp3表达量(P<0.05),其中5 mg/kg剂量的作用效果相对显著(P<0.05).结论:小剂量大黄酸可能通过抑制IL-2水平和促进Foxp3表达量,调控炎症反应和免疫功能,从而在EAE中发挥治疗作用.
    • 金桂花; 李红花; 李雪; 藤本·学; 张庆镐
    • 摘要: Objective:To investigate the role of B cell adoptor protein with ankyrin repeats ( BANK ) in experimental autoimmune encephalomyelitis ( EAE) .Methods: C57BL/6 mice and BANK-deficient ( BANK-/-) mice were immunized with MOG peptide in CFA,and then observed the clinical symptoms and pathological severity .Results: The percentages of CD4+T cells,CD8+T cells and regulatory T cells in brain and spleen were analyzed by flow cytometry .BANK-/-mice showed significantly higher score at the peak and the plateau phase compared with wild-type mice(P<0.05).HE staining showed more widespread areas of inflammation and demyelination in BANK-/-mice when compared to wild-type mice on day 16.In addition,the frequency of CNS-infiltrating CD8+T cells was markedly higher in BANK-/-mice than in wild-type mice.In addition,the percentage of CD8+T cells from spleen in BANK-/-mice was also increased compared with wild-type mice (P<0.05).By contrast,the percentage of regulatory T cells and the ratio of CD 4/CD8 T cells from spleen in BANK-/-mice were significantly lower than in wild-type mice(P<0.05).Conclusion:Thus,BANK expression in B cells can inhibit the development of EAE .%目的:探讨B细胞特异性衔接蛋白BANK(B cell adoptor protein with ankyrin repeats)在小鼠实验性自身免疫性脑脊髓炎(Experimental autoimmune encephalomyelitis,EAE)中的作用.方法:MOG35-55多肽免疫C57BL/6鼠和BANK缺陷(BANK-deficient,BANK-/-)鼠制备EAE模型,观察实验动物临床症状及中枢神经系统的病理学变化;提取小鼠脑组织及脾脏,经流式细胞术检测中枢神经系统及外周免疫器官中的CD4+T细胞、CD8+T细胞及调节性T细胞的变化.结果:BANK-/-鼠EAE临床症状评分明显高于C57BL/6鼠,且体重减轻明显(P<0.05);HE染色结果显示,BANK-/-鼠较C57BL/6鼠炎症感染灶明显增多.流式细胞术结果显示,相对于C57 BL/6鼠BANK-/-鼠中枢神经系统中CD8+T细胞百分比明显增多,而脾脏中调节性T细胞百分比明显减少,CD4/CD8比值倒置(P<0.05).结论:B细胞衔接蛋白BANK的表达抑制EAE炎症反应.
    • 王红; 刘祥; 许彦梅; 白向宁; 张玲; 陈曦; 范正轩; 缪以懋; 李新琼
    • 摘要: Objective To study the prevalence and characteristics of a new pathogen Escherichia albertii in human , animal - derived food , poultry and birds in Zigong city , Sichuan province . Methods Samples of beef, mutton, pork, chicken, duck, chicken intestine, duck intestine and birds′droppings were collected from markets and stool samples of diarrheal patients and their close contacts were collected from hospitals. The samples were enriched with EC broth and tested for the presence of eae gene by PCR. Each eae-positive enrichment culture was streaked on MacConkey agar. The eae-positive non-lactose fermenting strains were identified as Escherichia albertii by 16S rDNA sequencing and housekeeping genes analysis. Those strains were further analyzed by intimin and cdtB subtyping and pulsed-field gel electrophoresis ( PFGE) . Results Fifty-one strains were identified as Escherichia albertii, including 19 from duck intes-tines, 18 from chicken intestines, 3 from diarrheal patients, 3 from close contacts, 1 from egret excrement, 3 from chicken meat, 2 from duck meat, 1 from pork and 1 from mutton. Six intimin subtypes ( sigma, rho, iota2, epsilon3, nu and N5) were harbored by those strains. All 51 strains carried the Ⅱ/Ⅲ/Ⅴ subtype group of cdtB and among them, 3 strains possessed another copy of Ⅰ/Ⅳ subtype group. Results of PFGEshowed high genetic diversity with 40 different band patterns. Conclusion It is the first time that Escherich-ia albertii was identified in diarrheal patients, close contacts, egret, poultry and animal-derived food in Chi-na. It is practically important for understanding the etiology and epidemiology of Escherichia albertii in China.%目的 了解自贡地区人群、动物源性食品、家禽及鸟类携带艾伯特埃希菌情况及菌株特征.方法 采集市售牛肉、羊肉、猪肉、鸡肉、鸭肉、鸭肠及鸡肠,不同鸟类粪便及腹泻患者和密切接触人群粪便,经EC肉汤增菌后,PCR检测eae基因,阳性增菌液接种麦康凯琼脂,挑取不发酵乳糖、eae阳性菌落进一步通过16S rDNA测序及多位点序列分型分析(MLST),确定为艾伯特埃希菌,并对菌株进行eae、cdtB多态性分析及脉冲场凝胶电泳(PFGE)分型分析.结果 本研究共鉴定51株艾伯特埃希菌(19株来源于鸭肠及其内容物、18株来源于鸡肠及其内容物、3株来源于腹泻患者粪便、3株来源于密切接触人群粪便、1株来源于白鹭粪便、3株来源于鸡肉、2株来源于鸭肉、1株来源于猪肉、1株来源于羊肉).eae分为6种亚型,分别为sigma、rho、iota2、epsilon3,nu及N5,而51株艾伯特埃希菌均具有Ⅱ/Ⅲ/ⅤcdtB亚型,其中3株菌同时具有Ⅰ/ⅣcdtB亚型.51株分离株共分为40种PFGE带型,呈多态性分布.结论 首次在中国腹泻患者、密切接触人群、野生白鹭、家禽和动物源性食品中证实了艾伯特埃希菌的存在,对进一步深入开展艾伯特埃希菌病原学、流行病学研究具有重要实际意义.
    • 张玲; 刘祥; 许彦梅; 李新琼; 王红; 熊衍文
    • 摘要: 目的 了解长期从事鸡鸭等家禽养殖及屠宰人员等健康人群艾伯特埃希菌的携带情况.方法 收集家禽养殖、屠宰人群及其他健康人粪便,经EC肉汤增菌后PCR检测eae基因,阳性样品接种麦康凯琼脂,挑选不发酵乳糖菌落,通过16S rDNA序列分析和多位点序列分型(MLST)对菌株进行鉴定.分离株进行紧密粘附素亚型和cdtB亚型分析,并通过脉冲场凝胶电泳(PFGE)分析与动物来源艾伯特埃希菌菌株间的相关性.结果 从189份从事鸡鸭宰杀人员的粪便中,分离到2株艾伯特埃希菌,从58份其他健康人群粪便中分离到1株菌,而138份家禽养殖场人员粪便中未分离到菌株.3株菌株的紧密粘附素亚型分别为sigma,iota 2,nu,cdtB亚型均为II/ⅢI/Ⅴ亚型.PFGE显示三株菌之间的带型相似性小于80%,并且与鸡鸭等来源的艾伯特埃希菌带型不同.结论 从事鸡鸭屠宰等健康人员中存在一定程度的艾伯特埃希菌携带率,但其与家禽携带艾伯特埃希菌的关系,仍需进一步研究.%We investigated the carrying situation of Escherichia albertii from healthy people engaged in breeding and slaughtering poultry for a long time.We collected stool samples from people engaged in breeding and slaughtering poultry and other healthy people.After enriched with EC broth,eae-positive enrichment culture was directly streaked on MacConkey,and eaepositive lactose non-fermenting isolate was retained for further investigation.The 16S rDNA sequencing and multilocus sequence typing (MLST) were applied in the identification of E.albertii from suspected strains.Intimin subtypes and cdtB types of E.albertii strains were detected.Pulsed-field gel electrophoresis (PFGE) was used to detected genetic polymorphism of strains from this study and animal source ones.Results showed that two isolates were identified as E.albertii from 189 stools of people exposed to slaughtering chickens and ducks and one from 58 stools in control groups.No isolate was identified as E.albertii from 138 stools samples of people exposed to breeding poultry.Intimin subtypes of three isolates from stool samples were subtyped as sigma,iota 2,nu,and cdtB types were closely related to types Ⅱ/Ⅲ/Ⅴ.PFGE patterns of the three strains was distinguishable (<80% similarity),and appeared in different cluster with chickens,ducks and other sources of E.albertii strains.The rate of carrying E.albertii to a certain extent exist in healthy people engaged in slaughtering chickens and ducks,and the relationship between these strains and strains from poultry should be further investigated.
    • 陈晓香; 张俊华; 盛家和
    • 摘要: Objective:To investigate the change of thymus in different period of EAE mice. Methods: The thymic index and thymocyte number at 0,10,15,20 days after EAE induced were recorded. The percent of thymic apoptosis and CD4+CD44+T cells in spleen was acquired by Flow Cytometry. The content of p53 and Bcl-2 gene was detected by PCR and electrophoretic technique. Results:The thymic index and thymocyte number correspondingly reduced at 0,10,15 days after EAE induced. Apoptotic rate of thymocyte increased at 10,15 days after EAE induced,highest at 10 days. The percent of CD4+CD44+T cells also increased at 10,15 days after EAE induced, highest at 10 days. The content of p53 increased, while Bcl-2 reduced at 10 days after EAE induced. Conclusion:The atrophy of thymus is most serious at 15 days after induction;while the apoptotic percent is highest at 10 days after induction,which have a relationship with regulation of p53 and Bcl-2. The change of thymus in EAE mice closely related with EAE attack,and the recovery of thymus precede EAE.%目的::探讨胸腺在EAE小鼠不同临床时期的变化。方法:记录小鼠EAE模型诱导后第0、10、15、20天的胸腺指数和胸腺细胞数;应用流式细胞术观察胸腺细胞的凋亡比例和脾脏CD4+CD44+T细胞的比例;应用PCR和电泳技术观察凋亡因子p53和Bcl-2的含量变化。结果:EAE小鼠在第0、10、15天胸腺指数和胸腺细胞数相应地逐渐减少;第10、15天胸腺细胞凋亡率升高,第10天最高;CD4+CD44+T细胞比例在第10、15天升高,第10天最高;EAE诱导第10天胸腺细胞p53含量升高,而Bcl-2含量降低。结论:EAE小鼠诱导后第15天胸腺萎缩最严重,第10天凋亡率最高,并且与基因p53和Bcl-2调控有关;EAE小鼠胸腺变化与小鼠发病关系密切,并且胸腺又先于临床症状恢复。
    • 张荣博; 徐彬; 朱敏姿; 周未莹; 吴忧; 梁顺利; 章水晶; 李铮; 袁强
    • 摘要: [目的]研究山茱萸新苷对实验性自身免疫性脑脊髓炎( experimental autoimmune encephalomyelitis, EAE)大鼠中枢神经系统单核细胞趋化蛋白-1( monocyte chemoattractant protein-1,MCP-1)表达及CD68阳性细胞浸润的影响。[方法]制备豚鼠全脊髓匀浆免疫抗原,皮下注射至 Lewis大鼠,建立EAE模型。设正常对照组、EAE组、山茱萸新苷组、波尼松组,每天神经功能评分,待症状达到高峰处死实验动物,用RT-PCR、Western Blot法比较各组实验动物中枢神经系统MCP-1 mRNA及蛋白的表达,免疫组织化学染色法比较各组实验动物中枢神经系统 CD68阳性细胞浸润情况。[结果]正常对照组、EAE组、山茱萸新苷组、波尼松组大鼠MCP-1 mRNA的相对表达量分别为(11.265±2.928)、(401.373±55.398)、(124.987±20.244)、(75.465±7.766),MCP-1蛋白相对表达量分别为(7.458±2.570)、(24.155±1.420)、(19.568±0.863)、(17.458±1.630),CD68阳性指数分别为0%、(41.93±12.25)%、(16.08±8.70)%、(5.38±2.88)%。使用单因素方差分析法,MCP-1 mRNA的相对表达量、MCP-1蛋白相对表达量、CD68阳性指数组间差异显著,均有统计学意义( F=199.734、66.081、35.565,均P=0.000)。山茱萸新苷组与EAE组在神经功能评分、MCP-1 mRNA的相对表达量、MCP-1蛋白相对表达量、CD68阳性指数表达差异均有统计学意义( P=0.002、0.000、0.003、0.013)。[结论]山茱萸新苷可改善 EAE大鼠神经功能,抑制EAE大鼠中枢神经系统MCP-1表达及CD68阳性细胞浸润。%Objective] To explore the impact of cornuside on the expression of MCP-1 and the infiltration of CD68 positive cells in the central nervous system in EAE. [Methods] An EAE model was established by injecting the guinea pig spinal cord homogenate antigen in subcutaneous tissue of Lewis rats. The rats were randomly divided into normal control group, EAE group, cornuside group, and prednisone group. The neurological function scores were assessed every day. At last, these animals were killed when the symptoms reached the peak. The expressions of MCP-1 mRNA and MCP-1 protein in the central nervous system of each group were compared by using real-time quantitative PCR(RT-PCR) and Western Blot. Immunohistochemical staining was used to compare the infiltration of CD68 positive cells in the central nervous system of experimental animals in each group. [Results] The relative expression of MCP-1 mRNA by RT-PCR of normal control group, EAE group, cornuside group, prednisone group rats was respectively(11.265 ±2.928) (401.373 ±55.398), (124.987 ±20.244), (75.465 ±7.766), the relative expression of MCP-1 protein by Western Blotting was respectively(7.458 ±2.570), (24.155±1.420),(19.568±0.863),(17.458±1.630), and the CD68 positive indexes were respectively 0%,(41.93±12.25)%,(16.08±8.70)%,(5.38±2.88)%. Using one-way analysis of variance, there were significant statistical differences of the relative expression of MCP-1 mRNA, the relative expression of MCP-1 protein and CD68 positive index between the groups(F=199.734, 66.081, 35.565, all P=0.000). The difference in neurological function score, the relative expression of MCP-1 mRNA, the relative expression of MCP-1 protein and CD68 positive index between cornuside group and EAE group had statistical significance(P=0.002, 0.000, 0.003, 0.013). [Conclusion] Cornuside can improve neural function of EAE rats, also can inhibit the expression of MCP-1 and the infiltration of CD68 positive cells in the central nervous system of EAE rats.
    • 何展文; 刘木金; 孟哲; 李平甘; 罗向阳; 李栋方; 梁立阳
    • 摘要: 目的:观察异体骨髓间充质干细胞(BMSCs)移植后在EAE大鼠体内存活、增殖、分化,探讨BMSCs对EAE的神经再生的修复作用及迁徙分化情况。方法 SD雌性大鼠45只,随机分为3组,其中EAE模型组20只,正常对照组5只, EAE模型BMSCs移植组20只。重组免疫蛋白MBP68‐86诱导建立EAE的动物模型,在免疫后早期第5天静脉输注Wistar大鼠的BMSCs(4×106/只,0.4 mL)。观察输注后大鼠神经功能变化和组织学变化,利用免疫组化方法检测不同时间脑脊髓神经元特异性烯醇化酶(NSE)、胶质纤维酸性蛋白(GFAP)、2’,3’‐环腺苷酸‐3’‐磷酸二酯酶(CNPase)表达,观察BMSCs移植后EAE大鼠体内神经元、星形胶质细胞和少突胶质细胞数量。结果 EAE大鼠免疫后早期移植BMSCs ,神经功能评分无论是高峰期评分还是平均评分显著低于EAE模型组。BMSCs移植组在第7天NSE阳性细胞数较EAE模型组表达水平增多,但并无显著性差异,而第15天、第21天和第30天NSE阳性细胞数明显高于EAE模型组的表达水平(P<0.05)。BMSCs移植组各时间点CNPase染色阳性细胞数明显高于EAE模型组的表达水平(P<0.05),随着时间迁移,BMSCs移植组CNPase染色阳性细胞数表达逐渐增加。BMSCs移植组各个时间点GFAP阳性细胞数与EAE模型组比较无显著性差异。病理检查显示EAE大鼠免疫后早期移植BMSCs可使脑组织炎症反应减轻,脱髓鞘病灶的数目也明显少于EAE模型组。结论预防性静脉输注BM SCs可能通过免疫调节,抑制免疫反应所致的神经细胞损伤,减少神经元和少突胶质细胞的凋亡,从而发挥神经保护作用,但不能排除仍有部分BMSCs在局部微环境信号的诱导下向脱髓鞘区迁徙并分化为髓鞘形成细胞的可能。%Objective To examine the survival ,proliferation and differentiation of allogenic bone marrow mesenchymal stem cells(BMSCs) in EAE rats and to explore the mechanism of neuroprotection after transplantation with BMSCs. Methods Forty‐five SD female rats were randomly divided into three groups :EAE model group(n=20) ,control group (n=5) and BM‐SCs transplantation group (n=20). SD rats were immunized with MBP68‐86. Then BMSCs were administered intravenously on day 5 after immunization ,the dose of BMSCs was 4 × 106 (0.4 mL)for each rat. Throughout the study ,neurological symp‐toms of active disease and histopathologic examination were evaluated in rats. The expressions of NSE ,GFAP and CNPase in the spinal cord and the brain were detected by immunohistochemistry technique at different time ,and the number of neurons , astrocytes and oligodendrocytes in EAE rats after BMSCs transplantation were analyzed.Results Compared with EAE model group ,whether the peak neurofunctional scores or the mean neurofunctional scores of neural function evaluation during the course significantly decreased in BMSCs transplantation group. The number of NSE positive cells at 7th day after transplanta‐tion in BMSCs transplantation group were higher than that in EAE model group ,with no significant difference. The numbers of NSE positive cells at 15th ,21st and 30th day after transplantation in BMSCs transplantation group were higher than that in EAE model group(P<0.05). The number of CNPase positive cells at different day after transplantation in BMSCs transplanta‐tion group was higher than that in EAE model group(P<0.05). The number of CNPase positive cells increased gradually over time. Compared with EAE model group and control group ,the number of GFAP positive cells at different days after transplan‐tation showed no significant difference in BMSCs transplantation group. Pathologic results showed that the early transplanta‐tion of BMSCs in EAT rats could alleviate the inflammatory reaction participated in cerebral tissue ,and the number of demyeli‐nation decreased in BMSCs transplantation group compared with EAE model group. Conclusion The neuroprotective mecha‐nism of BMSCs by the prophylactic intravenous infusion in EAE rats is that BMSCs may inhibit cells injury ,decrease the apop‐tosis of neurons and oligodendrocytes through immunomodulation. We can’t rule out the possibility that some BMSCs may be migrated to the demyelinated foci and differentiated into oligodendrocytes on the condition of local microenvironment.
    • 孙寒晓; 胡志刚; 曹雅楠; 庄文芳; 宣彬彬; Igor Maricic; 盛慧明
    • 摘要: Objective To investigate the phenotype and the immunoregulatory function of CD8αα+TCRαβ+regulatory T cells in peripheral blood samples from mice.Methods The distribution profile and the phenotype of CD8αα+TCRαβ+regulatory T cells in C57BL/6 mice were detected by flow cytometry.The cytokines released by CD8αα+TCRαβ+regulatory T cells upon the stimulation with anti-CD3 antibody were analyzed by cytometric bead array.The in vitro immunosuppressive activity of CD8αα+TCRαβ+regulatory T cells on activated CD4+T cells was analyzed by using flow cytometry and carboxyfluorescein succinimidyl ester ( CFSE ) .An adoptive cell transfer assay was set up to evaluate the immunoprotective effects of CD8αα+TCRαβ+ regulatory T cells in a mouse model of experimental autoimmune encephalomyelitis ( EAE) .Results CD8αα+TCRαβ+regulatory T cells were detected in liver, spleen and peripheral blood samples collected from naïve C57BL/6 mice.Compared with CD8αβ+TCRαβ+regulatory T cells, CD8αα+TCRαβ+regulatory T cells showed a memory-activated phenotype of CD25+CD122high CD44high CD62Llow CD69high NK1.1+DX5+.CD8αα+TCRαβ+regulatory T cells could produce IL-2 after 24 hours stimulation with anti-CD3 antibody, followed by producing IFN-γ, TNF-α, IL-4, IL-17A and traces of IL-6 and IL-10. In vitro, CD8αα+TCRαβ+regulatory T cells specifically suppressed the proliferation of activated CD4+T cells ( P<0.01 ).Moreover, they could delay the onset of EAE in mice and reduce clinical score (P<0.01).Conclusion CD8αα+TCRαβ+regulatory T cells were a unique population with immunoregula-tory function, which could be used as a potential therapeutic target in the treatment of autoimmune disease.%目的:研究外周CD8αα+TCRαβ+调节性T细胞的表型和免疫调节功能。方法采用流式细胞术分析CD8αα+TCRαβ+T细胞在 C57BL/6J小鼠体内的分布情况,并对其进行了相关表型分析,随后采用anti-CD3抗体刺激,流式微球分析细胞因子分泌格局;采用流式细胞术分选和CFSE标记方法,在体外研究CD8αα+TCRαβ+T细胞调节抑制功能,并采用细胞过继免疫实验观察CD8αα+TCRαβ+T细胞对实验性变态反应性脑脊髓炎( EAE)小鼠模型的保护作用。结果在C57BL/6J小鼠肝脏、脾脏和外周血中存在一群 CD8αα+TCRαβ+T 细胞与CD8αβ+TCRαβ+T细胞相比具有CD25+CD122highCD44highCD62LlowCD69highNK1.1+DX5+记忆效应表型,激活后能迅速产生IL-2,随后产生IFN-γ、TNF-α、IL-4和IL-17A以及微量IL-6和IL-10。体外功能实验表明CD8αα+TCRαβ+T细胞专一性抑制活化CD4+T细胞的分化(P<0.01),体内实验证明该群细胞具有抑制自身活化CD4+T细胞介导的EAE,延缓疾病发展和保护的效果( P<0.01)。结论 CD8αα+TCRαβ+T细胞是体内一群固有的具有免疫调节功能的CD8+调节性T细胞,有望成为细胞治疗新靶点用于自身免疫性等各类疾病。
    • 寇爽; 王义周; 赵晖; 王蕾
    • 摘要: 目的:探讨实验性自身免疫性脑脊髓炎(experimental autoimmune encephalomyelitis,EAE)大鼠脑和脊髓中环磷酸腺苷反应元件结合蛋白(cAMP response element binding protein,CREB) mRNA和蛋白表达及左归丸和右归丸对其的调节作用.方法:将雌性Lewis大鼠随机分为正常组、模型组、激素组、左归丸组和右归丸组.给予正常组大鼠双后足垫注射生理盐水,其余各组注射髓鞘碱性蛋白(myelin bas-ic protein,MBP) 68-86抗原,免疫诱导EAE模型.分别灌胃给予相应的治疗药物或生理盐水.于14天(急性期)及28天(缓解期)分别取大鼠脑和脊髓,用实时荧光定量RT-PCR和Western-blot法检测CREB mRNA及蛋白的表达.结果:与正常组比较,EAE模型组大鼠脑和脊髓的CREB除了缓解期脑中蛋白的表达明显升高(P<0.05)外,其余均降低,特别是在急性期的大鼠脑中CREB mRNA及蛋白明显降低(P <0.05或P<0.01);急性期和缓解期脊髓中CREB mRNA也显著降低(P<0.01).与模型组比较,左右归丸组急性期大鼠脊髓CREB mRNA和缓解期蛋白均升高明显(P<0.05或P<0.01).左归丸组急性期大鼠脑CREB mRNA表达有显著上调(P<0.01),缓解期脑和急性期脊髓中的蛋白有明显上调(P <0.05或P<0.01).结论:左右归丸对EAE大鼠的中枢神经损伤后的修复作用可能与上调CREB mRNA和蛋白表达有关.但二方在作用时间、部位和靶点各有侧重.
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