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find Keyword "补体" 21 results
  • 补体因子H与老年性黄斑变性

    Release date:2016-09-02 05:48 Export PDF Favorites Scan
  • The Role of theComplement Receptor 1 and 3 on Neutrophils in Distinguishing Bacterial Infection in Patients with Acute Exacerbation of Chronic Obstructive Pulmonary Disease

    Objective To study the role of the complement receptor 1 and 3 ( CR1 and CR3) on neutrophils in distinguishing bacterial infection in patients with acute exacerbation of chronic obstructive pulmonary disease ( AECOPD) . Methods 40 patients with AECOPD were divided into two groups according to the detection of bacteria in subairway. 20 patients with stable COPD and 20 healthy subjects with no history of smoking were also included. According to Anthonisen criteria, 40 AECOPD patients weredivided into type Ⅰ( 11 cases) , type Ⅱ ( 12 cases) , and type Ⅲ( 17 cases) . The levels of CR1 and CR3 in blood were measured by flow cytometry. Results In AECOPD patients, 25 cases were detected bacteria,and 15 cases were not detected bacteria. The level of CR1 and CR3 were highest in the bacterial infection group than other groups, and highest in type Ⅰ AECOPD patients than other types. ROC analysis showed that CR1 and CR3 had good diagnostic value in bacterial infection in AECOPD, with optimal cutoff values of 11 and 52, respectively. Conclusion CR1 and CR3 may be good index of distinguishing bacterial infection in AECOPD.

    Release date:2016-08-30 11:53 Export PDF Favorites Scan
  • The role of complement signaling pathway in the pathogenesis of neuromyelitis optica

    Neuromyelitis optica (NMO) is a kind of demyelinating disorder that preferentially affects the optic nerves and spinal cord and results in permanent vision loss. NMO pathogenesis is thought to involve binding of anti-aquaporin-4 (AQP4) auto-antibodies to astrocytes, which causes complement-dependent cytotoxicity (CDC) and downstream inflammation leading to oligodendrocyte and neuronal injury. Vasculocentric deposition of activated complement is a prominent feature of NMO pathology. In recent years, a number of groups have found complements play an important role in the pathogenesis of NMO, and basic researches in NMO therapy due to its specificity and uniformity. Its inhibition would protect against proteins in the classical complement pathway so that cure the disease. This review will expound the the role of complement signaling pathway in the pathogenesis of NMO, and provide reference for a more in-depth understanding and clinical treatments of NMO.

    Release date:2019-05-17 04:15 Export PDF Favorites Scan
  • 阵发性睡眠性血红蛋白尿症的靶向治疗

    阵发性睡眠性血红蛋白尿症(PNH)是一种罕见的造血干细胞克隆性的溶血性疾病,目前治疗困难。重组人源型抗补体蛋白C5单克隆抗体(eculizumab)的出现及临床应用开启了PNH靶向治疗的新篇章。eculizumab通过与补体C5结合,防止C5裂解形成C5b及膜攻击复合物,减少溶血,降低输血需求,提高患者生活质量。2007年,eculizumab分别被美国食品和药物管理局、欧盟委员会通过用于治疗PNH血管内溶血。现对PNH患者使用eculizumab靶向治疗作一综述。

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  • 肝叶切除后胆汁免疫球蛋白和补体变化的临床意义

    Release date:2016-08-29 09:20 Export PDF Favorites Scan
  • 三种自身抗体和补体C3水平检测对狼疮性肾炎患者的诊断意义

    目的探讨抗心磷脂抗体(ACA)、抗核小体抗体、抗核糖体p蛋白抗体3种自身抗体与补体C3水平检测对狼疮性肾炎(LN)患者的诊断意义。 方法2005年7月-2010年12月对406例系统性红斑狼疮(SLE)患者(其中LN 122例)和120例健康体检者采用酶联免疫吸附测定法测定ACA,应用欧蒙印迹法测定抗核小体抗体和抗核糖体p蛋白抗体,应用散射比浊法测定补体C3水平。 结果ACA和抗核糖体p蛋白抗体阳性率在LN组均为21.31%,在非LN组分别为17.61%、14.08%,差异无统计学意义(P>0.05);抗核小体抗体在LN组为56.56%,在非LN组为39.08%,差异有统计学意义(P<0.05);LN组和非LN组3种抗体阳性率与对照组比较差异有统计学意义(P<0.01);LN组、非LN组和对照组补体C3水平分别为(0.52±0.22)、(0.67±0.29)、(1.28±0.32)g/L,3组比较差异均有统计学意义(P<0.01);LN组ACA、抗核小体抗体和抗核糖体p蛋白抗体同时阳性率(10.66%)高于非LN组(3.17%),差异有统计学意义(P<0.05)。 结论ACA、抗核小体抗体、抗核糖体p蛋白抗体及补体C3的联合检测对狼疮性肾炎的诊断及鉴别诊断、预后判断等方面具有一定意义。

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  • CLINICAL STUDY ON SERUM COMPLEMENT-3 AND PLASMA FIBRONECTIN OF PATIENTS WITH OBSTRUCTIVE JAUNDICE PRE- AND POST-OPERATION

    Thirty patients with obstructive jaundice were investigated for serum complement-3 (C3) and plasma fibronectin (FN).The levels of C3 and FN of the juandiced patients were higher than that of thirty patients without obstructive jaundice (P<0.01). As compared to pre-operation, the level of C3 of the jaundiced patients decreased obviously within two weeks after operation(P<0.01), and recovered in the third week after operation. The level of FN of the juandice patients decreased evidently within one week(P<0.01), and recovered in the second week after operation. However, the levels of C3 and FN of the patients without obstructive jaundice changed slightly after operation (P<0.05). The high levels of C3 and FN of jaundiced patients may be relative to the latent infection. Consumption and immune imparing may be the reasons of C3 and FN to decrease.

    Release date:2016-08-29 03:44 Export PDF Favorites Scan
  • The genetic predisposition of complement C5 gene polymorphisms in proliferative diabetic retinopathy in Chongqing Han population

    Objective To observe the genetic predisposition of complement C5 gene polymorphisms in proliferative diabetic retinopathy (PDR) in Chongqing Han population. Methods 400 type 2 diabetes (T2D) patients (case group) and 600 age- and sex-matched healthy controls (control group) were enrolled in this study. There were 8 PDR patients in case group. All the subjects were Han ethnic people. The immune-related representative SNP locus of C5 gene including rs2269067, rs7040033, rs7027797 were screened by linkage disequilibrium analysis. Locus rs1017119 was selected by TagSNP and was around the above three loci. Subjects′ peripheral venous blood was collected and DNA was extracted. Genotyping was examined by PCR-restriction fragment length polymorphism method. The level of C5 plasma protein was measured by enzyme-linked immunoabsorbent assay. Results The frequency of GG genotype of rs2269067 was significantly increased in PDR patients in cases group compared with controls (Pc=3.4×10-5, OR=1.87, 95%CI=1.43 - 2.44;P=3.1×10-6). There was no differences in frequency of G, CC and CG genotype of rs2269067 between two groups (P=1.4×10-4, 1.000, 1.0×10-6). There were no differences in frequency of G, CC, CG, GG genotype of rs7040033, rs1017119, and rs7027797 between two groups (P > 0.05). The production of C5 plasma protein was significantly increased in case group as compare with control group (P=0.0004). An increased production of C5 plasma protein was observed in rs2269067 GG genotype cases compared to CG or CC cases (P=0.003, 0.001). Conclusion C5 rs2269067 GG genotype may be associated with the PDR of T2D in Chongqing Han population.

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  • 补体系统在老年性黄斑变性发病机制中的作用

    补体系统是机体固有免疫的重要组成部分,包含分布于血浆中或细胞表面的40多种物质,可通过经典途径、凝集素途径或替代途径激活。补体系统通过炎症免疫、血管内皮生长因子表达上调、氧化应激等途径参与和影响老年性黄斑变性(AMD)的发生发展过程;其相关分子的基因多态性与AMD的易感性息息相关;靶向补体系统的治疗对AMD也有一定的疗效。补体系统与AMD相互关系的研究将有助于进一步阐明AMD的发病机制并为其治疗提供新的方向。

    Release date:2016-09-02 05:26 Export PDF Favorites Scan
  • 补体在渗出型老年性黄斑变性中的作用研究进展

    补体系统是机体免疫系统的重要组成部分,广泛参与机体抗微生物防御反应,清除凋亡细胞和免疫复合物以及维持组织稳态,进行免疫调节。补体系统与老年性黄斑变性(AMD)发生也密切相关。在玻璃膜疣中,含有多种选择激活途径中的蛋白;补体成分基因变异也使AMD的发病风险大大增加。补体系统多种分子与AMD CNV形成关系密切,针对补体系统异常激活的治疗可能为渗出型AMD的治疗带来新的曙光。

    Release date:2016-09-02 05:26 Export PDF Favorites Scan
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