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1
Human anti-IgM iso-antibodies in subjects with selective IgA deficiency.选择性IgA缺乏症患者体内的人抗IgM同种抗体。
Clin Exp Immunol. 1972 Nov;12(3):305-13.
2
Antibodies to human collagen in subjects with selective IgA deficiency.选择性IgA缺乏症患者体内针对人胶原蛋白的抗体。
Clin Exp Immunol. 1973 Feb;13(2):203-8.
3
Autoimmunity in selective IgA deficiency.选择性IgA缺乏症中的自身免疫
Birth Defects Orig Artic Ser. 1975;11(1):144-6.
4
Immunologic responses to bacteriophage phi-X 174 in immunodeficiency diseases.免疫缺陷疾病中对噬菌体phi-X 174的免疫反应。
J Clin Invest. 1971 Dec;50(12):2559-68. doi: 10.1172/JCI106756.
5
Immunobiology of human anti-IgM iso-antibodies. I. Clinical and serological studies.
Clin Immunol Immunopathol. 1973 Jan;1(2):257-69. doi: 10.1016/0090-1229(73)90026-3.
6
[A contribution to the immunology of the Louis-Bar syndrome: observations from one family].[对共济失调毛细血管扩张症免疫学的贡献:来自一个家族的观察]
Monatsschr Kinderheilkd (1902). 1970 Apr;118(4):123-7.
7
Membrane receptors and in vitro responsiveness of lymphocytes in human immunodeficiency.人类免疫缺陷中淋巴细胞的膜受体与体外反应性
J Immunol. 1974 Jan;112(1):376-86.
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[Type IV dysgammaglobulinemia associated to autoimmune processes].
Schweiz Med Wochenschr. 1970 Nov 14;100(46):1988-90.
9
Analysis of immunoglobulin deficiency cases: a five year study.免疫球蛋白缺乏症病例分析:一项为期五年的研究。
Indian J Pathol Microbiol. 1997 Jul;40(3):309-13.
10
Identification and clinical implications of isoantibodies in patients with idiopathic dysgammaglobulinemia.
Transfusion. 1973 Sep-Oct;13(5):291-6. doi: 10.1111/j.1537-2995.1973.tb05491.x.

引用本文的文献

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The natural history of ataxia-telangiectasia (A-T): A systematic review.共济失调毛细血管扩张症(A-T)的自然病史:系统评价。
PLoS One. 2022 Mar 15;17(3):e0264177. doi: 10.1371/journal.pone.0264177. eCollection 2022.
2
Antibodies to human collagen in subjects with selective IgA deficiency.选择性IgA缺乏症患者体内针对人胶原蛋白的抗体。
Clin Exp Immunol. 1973 Feb;13(2):203-8.
3
Comparative study of bone marrow and blood B cells in infantile and acquired agammaglobulinemia. Possible role of circulating anti-IgM in pathogenesis.婴儿期和获得性无丙种球蛋白血症中骨髓和血液B细胞的比较研究。循环抗IgM在发病机制中的可能作用。
J Clin Invest. 1973 Sep;52(9):2218-24. doi: 10.1172/JCI107407.

本文引用的文献

1
A Low Molecular Weight Immunoglobulin Antigenically Related to 19 S IgM.与 19 S IgM 抗原相关的低分子量免疫球蛋白。
J Clin Invest. 1967 Aug;46(8):1329-37. doi: 10.1172/JCI105625.
2
Studies on the serum gamma-A-globulin level. 3. The frequency of A-gamma-A-globulinemia.血清γ-A球蛋白水平的研究。3. A-γ-A球蛋白血症的发生率。
Scand J Clin Lab Invest. 1965;17(4):316-20. doi: 10.3109/00365516509077057.
3
Isolated severe gamma A deficiency: immunoglobulin levels, clinical disorders, and chromosome studies.孤立性严重γA缺乏症:免疫球蛋白水平、临床疾病及染色体研究
J Lab Clin Med. 1970 Feb;75(2):307-15.
4
Human antibodies against bovine immunoglobulin M in IgA deficient sera.IgA 缺陷血清中针对牛免疫球蛋白 M 的人抗体。
Clin Exp Immunol. 1971 Jul;9(1):3-10.
5
Isoantibodies to human IgM: serologic and immunochemical investigations.
J Immunol. 1971 May;106(5):1147-53.
6
Human antibodies to ruminant IgM concealing the absence of IgA in man.
J Lab Clin Med. 1971 Apr;77(4):629-38.
7
Characterization of precipitating antibodies to ruminant serum and milk proteins in humans with selective IgA deficiency.选择性IgA缺乏症患者体内针对反刍动物血清和乳蛋白沉淀抗体的特征分析。
N Engl J Med. 1971 Jan 7;284(1):7-10. doi: 10.1056/NEJM197101072840102.
8
Immunochemical quantitation of antigens by single radial immunodiffusion.通过单向辐射免疫扩散法对抗原进行免疫化学定量。
Immunochemistry. 1965 Sep;2(3):235-54. doi: 10.1016/0019-2791(65)90004-2.
9
Selective IgA deficiency: presentation of 30 cases and a review of the literature.选择性IgA缺乏症:30例病例报告及文献综述
Medicine (Baltimore). 1971 May;50(3):223-36.
10
Incidence of isolated deficiency of IgA in the serum of Canadian children.加拿大儿童血清中孤立性IgA缺乏症的发病率。
Ann Allergy. 1972 Jan;30(1):11-23.

选择性IgA缺乏症患者体内的人抗IgM同种抗体。

Human anti-IgM iso-antibodies in subjects with selective IgA deficiency.

作者信息

Wells J V, Bleumers J F, Fudenberg H H

出版信息

Clin Exp Immunol. 1972 Nov;12(3):305-13.

PMID:4629949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1553589/
Abstract

IgG-class iso-antibodies against human IgM (reverse rheumatoid factors') were detected in titres from 1:4 to 1:1024 in the serum of twelve of forty subjects (30%) with selective IgA deficiency. The antibodies were detected in a haemagglutination system with red cells coated by the chromic chloride method with proteins from a panel including nineteen Waldenström macroglobulins. The forty subjects included seventeen normal subjects, ten with recurrent infections, seven with ataxia telangiectasia, two each with asthma and lymphoma and one each with rheumatoid arthritis and chronic active hepatitis. Four of the twelve positive sera contained class-specific anti-IgM' which reacted with all or most of the IgM coats. The eight sera containing `anti-IgM of limited specificity' included six reacting with only one IgM coat, one reacting with two IgM coats and one reacting with four IgM coats. The anti-IgM in the latter serum defined an inherited allotypic marker on these four IgM proteins. There was no significant correlation between the presence of anti-IgM antibodies and the clinical status, sex and age of the patient nor the presence of antibodies against human IgG, human IgA and ruminant proteins. These antibodies against human IgM represent yet another immunologic abnormality in this group of patients.

摘要

在40名选择性IgA缺乏症患者中,有12名(30%)的血清中检测到了抗人IgM的IgG类同种抗体(“反向类风湿因子”),滴度从1:4到1:1024。这些抗体是在一个血凝系统中检测到的,该系统使用氯化铬法用包括19种瓦尔登斯特伦巨球蛋白在内的一组蛋白质包被红细胞。这40名受试者包括17名正常受试者、10名反复感染患者、7名共济失调毛细血管扩张症患者、2名哮喘患者、2名淋巴瘤患者、1名类风湿性关节炎患者和1名慢性活动性肝炎患者。12份阳性血清中有4份含有“类特异性抗IgM”,可与所有或大多数IgM包被发生反应。8份含有“特异性有限的抗IgM”的血清中,6份仅与一种IgM包被发生反应,1份与两种IgM包被发生反应,1份与四种IgM包被发生反应。后一份血清中的抗IgM定义了这四种IgM蛋白上的一种遗传同种异型标记。抗IgM抗体的存在与患者的临床状态、性别和年龄以及抗人IgG、抗人IgA和抗反刍动物蛋白抗体的存在之间没有显著相关性。这些抗人IgM抗体代表了这组患者中的又一种免疫异常。