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本文引用的文献

1
The distribution of microsomal and thyroglobulin antibody activity among the IgG subclasses.微粒体抗体和甲状腺球蛋白抗体活性在免疫球蛋白G亚类中的分布情况。
Clin Exp Immunol. 1984 Jul;57(1):239-43.
2
Predominance of IgG3 subclass in primary cirrhosis.原发性胆汁性肝硬化中IgG3亚类占优势。
Br Med J (Clin Res Ed). 1983 Mar 26;286(6370):1015-6. doi: 10.1136/bmj.286.6370.1015-a.
3
NIH conference: Primary biliary cirrhosis: a model autoimmune disease.美国国立卫生研究院会议:原发性胆汁性肝硬化:一种典型自身免疫性疾病。
Ann Intern Med. 1983 Oct;99(4):500-12. doi: 10.7326/0003-4819-99-4-500.
4
Monoclonal antibodies (McAbs) to determinants on human gamma chains: properties of antibodies showing subclass restriction or subclass specificity.针对人γ链上决定簇的单克隆抗体(McAbs):表现出亚类限制或亚类特异性的抗体特性。
Immunology. 1982 Oct;47(2):329-36.
5
Enhanced binding of neuraminidase-treated sheep erythrocytes to human T lymphocytes.神经氨酸酶处理的绵羊红细胞与人类T淋巴细胞的结合增强。
Blood. 1973 Dec;42(6):939-46.
6
Quantitation of immunoglobulin classes and subclasses in anti-Rh (D) antibodies.抗 Rh(D)抗体中免疫球蛋白类别和亚类的定量分析。
Vox Sang. 1985;48(6):350-6. doi: 10.1111/j.1423-0410.1985.tb00195.x.
7
Positive antimitochondrial antibody but normal alkaline phosphatase: is this primary biliary cirrhosis?抗线粒体抗体阳性但碱性磷酸酶正常:这是原发性胆汁性肝硬化吗?
Hepatology. 1986 Nov-Dec;6(6):1279-84. doi: 10.1002/hep.1840060609.
8
Assessment of the potential pathogenicity of type II collagen autoantibodies in patients with rheumatoid arthritis. Evidence of restricted IgG3 subclass expression and activation of complement C5 to C5a.
Arthritis Rheum. 1986 Nov;29(11):1316-21. doi: 10.1002/art.1780291103.
9
IgG subclasses in viral infections.病毒感染中的IgG亚类
Monogr Allergy. 1986;19:134-43.
10
IgG subclasses of autoantibodies in systemic lupus erythematosus, Sjogren's syndrome, and drug-induced autoimmunity.系统性红斑狼疮、干燥综合征及药物性自身免疫中自身抗体的IgG亚类
J Immunol. 1986 Oct 15;137(8):2528-34.

原发性胆汁性肝硬化患者的淋巴细胞在培养时会自发分泌高水平的IgG3。

Lymphocytes from patients with primary biliary cirrhosis spontaneously secrete high levels of IgG3 in culture.

作者信息

Bird P, Calvert J E, Mitchison H, Ling N R, Bassendine M, James O F

机构信息

Department of Pathology, University of Newcastle-upon-Tyne, UK.

出版信息

Clin Exp Immunol. 1988 Mar;71(3):475-80.

PMID:3133143
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1541685/
Abstract

The origin of the raised serum IgG3 in primary biliary cirrhosis has been examined. Blood lymphocytes from patients with PBC and from age- and sex-matched controls were cultured, and the culture supernatants were assayed for IgG and IgG3. Lymphocytes from PBC patients spontaneously synthesized a higher percentage IgG3/total IgG than did control lymphocytes, as determined by ELISA. The increased synthesis of IgG3 in culture correlated with serum IgG3 in the patients. This strongly suggests that the raised serum IgG3 in these patients is due to increased synthesis of this isotype. Following PWM stimulation, the proportion of IgG3/IgG synthesized by normal (and most PBC) lymphocytes increased and the difference in IgG3 synthesized by PBC and control lymphocytes became less marked. The kappa/lambda light chain ratio of the IgG3 was assayed by ELISA but no evidence was found for clonally restricted synthesis of IgG3 by PBC blood lymphocytes.

摘要

对原发性胆汁性肝硬化患者血清IgG3升高的原因进行了研究。对原发性胆汁性肝硬化患者以及年龄和性别匹配的对照者的血液淋巴细胞进行培养,并对培养上清液中的IgG和IgG3进行检测。通过酶联免疫吸附测定法(ELISA)测定,原发性胆汁性肝硬化患者的淋巴细胞自发合成的IgG3占总IgG的百分比高于对照淋巴细胞。培养物中IgG3合成的增加与患者血清IgG3相关。这有力地表明,这些患者血清IgG3升高是由于该同种型合成增加所致。在经美洲商陆有丝分裂原(PWM)刺激后,正常(以及大多数原发性胆汁性肝硬化患者)淋巴细胞合成的IgG3/IgG比例增加,原发性胆汁性肝硬化患者和对照淋巴细胞合成的IgG3差异变得不那么明显。通过ELISA检测IgG3的κ/λ轻链比例,但未发现原发性胆汁性肝硬化患者血液淋巴细胞克隆性受限合成IgG3的证据。