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find Keyword "自身免疫" 58 results
  • Studies on Induction of Experimental Autoimmune Thyroiditis with Excessive Iodine and Thyroglobulin in Rats

    【Abstract】Objective To study the relation between iodine and experimental autoimmune thyroiditis(EAT). Methods Establishment of animal model was performed with iodine and thyroglobulin(TG).The rats were randomly divided into 5 groups: normal control group(NC), low iodine group (LI,500 μg/L), high iodine group(HI,500 mg/L), TG+Freund adjuvant group(TG) and TG+Freund adjuvant+HI group(TG+HI). The rats in TG group and TG+HI group were rejected hypodermically with TG emulsified by complete Freund adjuvant, and strengthen immunity was conducted with TG emulsified by incomplete Freund adjuvant on 15 days. After that, strengthen immunity was done weekly till the end of the experiment. Serum TGAb and TPOAb were measured by radioimmunoassay. Observation of the pathological changes of thyroid gland was also done. Results Thyroid follicular destruction and lymphocytic infiltration in the TG+HI group (3.83±1.72) and HI group (3.00±0.89) were significantly higher than that of the NC group(0.67±0.82),P<0.05. The results of the TG group were higher compared with the NC group, but there were no significant differences between them(Pgt;0.05). The levels of TGAb in the TG+HI (4.990±1.505),HI (3.589±1.240) and TG group (4.883±1.198) were significant higher than those of the NC group (0.642±0.454) and the LI group (0.707±0.240),P<0.01. The levels of TPOAb in TG+HI group (1.475±0.523) and TG group (1.316±0.606) were significantly higher than those of the NC group (0.365±0.196) and the LI group(P<0.01). Serum TGAb and TPOAb levels were positively correlated with the histological grades of lymphocytic thyroiditis(r=0.9,P<0.05). Conclusion Excessive iodine intake may induce the occurrence of EAT. The induction of EAT with excessive iodine and TG may be more efficient.

    Release date:2016-08-28 04:44 Export PDF Favorites Scan
  • MIDDLE- AND LONG-TERM EFFECTIVENESS OF PRIMARY TOTAL HIP ARTHROPLASTY FOR PATIENTS WITH CHRONIC AUTOIMMUNE INFLAMMATORY DISEASE

    ObjectiveTo evaluate the middle- and long-term effectiveness of primary total hip arthroplasty (THA) in patients with chronic autoimmune inflammatory diseases. MethodsBetween January 1990 and June 2006, 42 patients (51 hips) with chronic autoimmune inflammatory diseases underwent THA. There were 15 males (18 hips) and 27 females (33 hips) with an average age of 36.9 years (range, 22-70 years). The locations were the left side in 29 hips and the right side in 22 hips. Of 42 cases, there were 11 cases of systemic lupus erythematosus (13 hips), 16 cases of rheumatoid arthritis (22 hips), and 15 cases of ankylosing spondylitis (16 hips). The causes of THA included avascular necrosis of the femoral head in 26 cases (34 hips), ankylosis of the hip in 15 cases (16 hips), and fracture of the femoral neck in 1 case (1 hip). The Harris score was 32.49 ± 9.50. The physical component summary (PCS) and mental component summary (MCS) of short form 36 health survey scale (SF-36) scores were 25.53 ± 4.46 and 42.28 ± 6.27, respectively. ResultsAll incisions healed primarily. All 42 patients were followed up 5-21 years (mean, 9.1 years). At last follow-up, the Harris score was 89.25 ± 8.47; PCS and MCS of the SF-36 were 51.35 ± 4.28 and 55.29 ± 8.31, respectively; and significant differences in the scores were found between pre- and post-operation (P lt; 0.05). Complications included limp (4 cases), prosthesis dislocation (2 cases, 2 hips), periprosthetic fracture (1 case, 1 hip), aseptic loosening (2 cases, 2 hips), and ectopic ossification (3 cases, 3 hips). ConclusionTHA seems to be a good choice for patients with chronic autoimmune inflammatory diseases.

    Release date:2016-08-31 05:39 Export PDF Favorites Scan
  • Clinical study of autoimmune optic neuropathy

    Objective〓〖WTBZ〗To observe the clinical features of autoimmune optic neuropathy (AON). 〖WTHZ〗Methods〓 〖WTBZ〗The clinical data of 58 patients with AON from Jan. 2006 to Dec. 2007 were retrospectively analyzed. The patients had undergone routine ophthalmological, neurological examination, visual field test, all set of autoimmune antibody test, brain MRI. 〖WTHZ〗Results〓〖WTBZ〗In 93 eyes of 58 patients with AON, the lowest best corrected visual acuity (BCVA) was lt;01 in 68 eyes (731%), 10 patients (172%) had other symptoms of nervous system, 14 patients (241%) had lesions of nonneurological system. Positive antinuclear antibody was found in 43 patients (796%); other abnormal antibodies were also found, including antiSSA/SSB, antidsDNA, antihistonic, anticardiolipin, and antihuman leukocyte antigen B27 antibodies. Systematic connective tissue disease presented in 20 patients (345%), such as sicca syndrome, systemic lupus erythematosus, and Behcet disease. 32 patients (552%) had abnormal brain MRI, and the BCVA of 49 eyes (777%) improved significantly after hospitalization. 〖WTHZ〗Conclusion〓〖WTBZ〗Patients with AON always have poor visual function, some of whom associate with other systems, as well as damages to other parts of the nervous system. While some AON patients are secondary to systemic connective tissue disease involving the optic nerve, the majority of these patients are isolated autoimmune optic neuropathy.

    Release date:2016-09-02 05:43 Export PDF Favorites Scan
  • Effects of testosterone on optic nerve and retinal ganglion cells in experimenta l autoimmune encephalomyelitis

    Objective:To observe the effects of testosterone on optic nerve an d retinal ganglion cells (RGC) in experimental autoimmune encephalomyelitis (EAE ). Methods:Fourty one female Wistar rats were randomly divide d into 3 groups: the normal group (10 rats), the untreated control group (15 rats) and the testos terone group (16 rats). The rats in the first two groups were fed with 1% ethano l every day, and the rats in the testosterone group were fed with methyltestoste rone (0.25 mg/kg) every day. On the 20th day, EAE model was induced in the untre ated control group and the testosterone group by injecting guinea pig spinal cor d homogenate in complete Freund's adjuvant and bordetella pertussis vaccine. RGC were labeled with flurogold (FG) by injecting it in superior colliculus and lat eral geniculate body 7 days before establishing EAE model. All rats were fed wit h drugs continuously, and after 1430 days, rats in normal group and rats in un t reated control and testosterone groups who had symptoms within 48~72 hours were observed by light microscopy and flash visual evoked potential (FVEP) to detect the functional and morphological changes of optic nerve. The number of RGC was counted by fluorescence microscopy,and apoptosis of RGC was observed by termina l deoxynucleotidyl transferasemediated biotinylated UTP nick end labeling (TUN E L) Results:EAE rats presented weakness or paralysis of tail a nd hind limbs 10 days after establishing EAE model. Compared with the rats in the untreated contr ol group, the rats in the testosterone group had longer disease delitescence and lower clinical score (P=0.042). Extensive demyelination of optic nerves wi th the circuitous configuration was found in the untreated control group; while mild demyelination of optic nerves with regular figure was found in the testosterone group. In the testosterone group, the latency of N1、P and N2 wave was shorter w hile the amplitude ofN1-P and P-N2was higher than that in the untreated cont rol group (Plt;0.05). The number of RGC was (2284plusmn;132), (934plusmn;78, and (1725 plusmn;95)cells/mm2 in the normal, untreated control and testosterone groups, respectively; w hich was higher in testosterone group than that in untreated control group (P=0.028). The number of TUNEL positive cells was (4.02plusmn;0.16), (24.44plusmn;2.22), and (9.84plusmn;2.36) cells per high power field (times;400) in the 3 grou ps, respectively; wh ich was less in testosterone group than that in untreated control group (P=0.025). Conclusions:Testosterone may reduce the incidence and clinical score of EAE, inhibit the apoptosis of RGC, alleviate the demyelinatio n of optic nerves, and improved the conduction function of optic nerves.

    Release date:2016-09-02 05:48 Export PDF Favorites Scan
  • 自身免疫葡萄膜炎的免疫学机制

    视网膜的自身免疫受中枢耐受、外周耐受和局部免疫赦免三种不同水平的调控。自身反应性T淋巴细胞是自身免疫葡萄膜炎的主要介导细胞。根据分泌细胞因子模式的不同将其分为Th1和Th2两种不同的亚群,这两种细胞分别通过不同的反应形式影响葡萄膜炎的发生和发展。发病过程中非特异性炎症细胞在局部的聚集及其所分泌的介质在局部组织损伤过程中起着非常重要的作用。阐明发病过程的不同环节和发展新型免疫干预策略将是未来的主要研究方向。 (中华眼底病杂志,2001,17:252-254) 

    Release date:2016-09-02 06:03 Export PDF Favorites Scan
  • 白细胞介素-35在自身免疫性疾病中的研究进展

    白细胞介素(IL)-35是IL-12家族中新的一员,由EB病毒诱导基因3产物(Ebi3)和IL-12p35亚基形成的异二聚体,它可由调节性T(Treg)细胞特异性产生,是Treg细胞介导的免疫调节作用所必需的细胞因子。增加IL-35可抑制一些自身免疫性疾病如动物模型中的CIA等,证明了它在炎性细胞因子介导的疾病中存有潜在的治疗作用。但是,很多和IL-35相关的问题仍然不清楚,比如IL-35的受体结构、介导的细胞信号通路、以及在人细胞中的表达模式。虽然IL-35与IL-12家族中的IL-12和IL-27有共同亚基,然而IL-35有着不同的生物学功能,因此拟通过对既往有关IL-12家族的许多室验结论进行再评价,以期望探索IL-35在其中所起到的作用。

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  • 白细胞介素-33在自身免疫性疾病发病机制中的作用研究进展

    自身免疫性疾病(AID)是由自身免疫应答引起的慢性炎症性疾病,该类疾病大多数原因不明,可能与遗传、感染及环境等因素有关。白细胞介素-33(IL-33)作为一种炎性细胞因子,通过IL-33/ST2信号通路调节免疫应答,从而参与疾病的发生和发展。AID的病程一般较长并反复迁延,临床治疗困难。研究IL-33与AID之间的关系,为AID致病机理的研究、疾病的诊断和治疗提供新的方向。

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  • The Change of Serum Interleukin-2 and Interleukin-12p40 in Patients with Grave’s Disease after Treatment with 131I and Its Significance

    目的 探讨Grave病患者采用131I治疗前后血清中白细胞介素-2(IL-2)及白细胞介素-12 p40(IL-12p40)含量的改变及细胞因子在该疾病中的作用与意义。 方法 采用酶联免疫吸附试验双抗夹心法、放射免疫法,对2009年10月-2011年12月收治的28例Grave病患者(治疗组)经131I治疗前后血清中IL-2和IL-12p40含量进行自身对比及与健康志愿者(对照组)对比;同时对治疗组患者治疗前、后的血清游离三碘甲腺原氨酸(FT3)、血清游离甲状腺素(FT4)、促甲状腺激素(TSH)水平与对照组进行对比。 结果 治疗后患者血清中IL-2和IL-12p40的水平为(19.54 ± 11.17)、(615.88 ± 349.32) ng/mL,明显高于治疗前(P<0.05),且与对照组比较差异无统计学意义(P>0.05);患者治疗前后血清中IL-2和IL-12p40水平与FT3、FT4水平有显著相关性。 结论 血清IL-2和IL-12p40可能共同参与Grave病的发病过程,并且这两种因子的水平与FT3、FT4水平呈负相关性。

    Release date:2016-09-08 09:18 Export PDF Favorites Scan
  • 辅助性T细胞17和实验性自身免疫性葡萄膜炎

    【摘要】 辅助性T细胞17(T-helper type 17,Th17)是一种以分泌白介素-17(IL-17)为特征的辅助性T淋巴细胞亚型,在自身免疫性疾病中的作用逐渐得到重视。葡萄膜炎是最常见的致盲眼病,一直是眼科研究的热点和难点。实验性自身免疫性葡萄膜炎(experimental autoimmune uveoretinitis, EAU)是葡萄膜炎研究的成熟动物模型,有关Th17和EAU关系的研究处于起步阶段,现就这方面的研究现状进行综述,为葡萄膜炎的免疫机制研究提供新思路。

    Release date:2016-09-08 09:24 Export PDF Favorites Scan
  • 自身免疫性胰腺炎诊疗进展

    【摘要】 自身免疫性胰腺炎是一种以免疫介导、纤维炎症改变为特点的特殊类型慢性胰腺炎。此病的特点为血清中高IgG4水平,伴胰腺肿大和胰管不规则狭窄,同时碳酸酐酶抗体和抗乳铁蛋白抗体的存在。病理学表现为导管周围淋巴浆细胞浸润伴纤维化。实验室、组织学检查、临床表现均显示与自身免疫有关。皮质激素对其疗效显著。日本、韩国、美国相继制定了自身免疫性胰腺炎的诊断标准,2008年提出了亚洲诊断标准。目前我国自身免疫性胰腺炎的病例报道不多,他国的诊断标准可作为我国自身免疫性胰腺炎诊疗的良好借鉴。

    Release date:2016-09-08 09:26 Export PDF Favorites Scan
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