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人类针对替代途径C3转化酶自身抗体的抗独特型抗体反应。

Human anti-idiotypic antibody responses to autoantibody against the alternative pathway C3 convertase.

作者信息

Spitzer R E, Stitzel A E, Tsokos G C

机构信息

Department of Pediatrics, State University of New York, Health Science Center, Syracuse 13210.

出版信息

Clin Immunol Immunopathol. 1990 Oct;57(1):19-31. doi: 10.1016/0090-1229(90)90019-m.

DOI:10.1016/0090-1229(90)90019-m
PMID:2394034
Abstract

Anti-idiotypic antibodies to autoantibody against the alternative pathway C3 convertase (C3NeF) were isolated and purified from normal human serum as well as from serum from six patients with membrano-proliferative glomerulonephritis (MPGN). All preparations of anti-id antibody blocked C3NeF deposition on EC3bBb as well as C3NeF stabilization of EC3bBb functional activity. The Ka of these ant-id antibodies for C3NeF was 10(9) liters/mol which is comparable to the Ka of C3NeF for its antigen. In addition, 90% of anti-id antibody isolated from patients with MPGN and 20% isolated from normal individuals resembled Bb and bound to C3b as well as to antibody specific for the Bb portion of Factor B. These anti-id antibodies also resembled C3b and bound to antibody specific for the C3c portion of C3b. Immunization of rabbits with this latter form of anti-id antibody led to the production of functionally active C3NeF. These data indicate that C3NeF anti-idiotypic antibodies exist in two distinct forms, with and without internal imagery of C3bBb, and can occur in both normal individuals and patients with MPGN.

摘要

从正常人血清以及六名膜增生性肾小球肾炎(MPGN)患者的血清中分离并纯化了针对替代途径C3转化酶自身抗体(C3NeF)的抗独特型抗体。所有抗独特型抗体制剂均能阻断C3NeF在EC3bBb上的沉积以及EC3bBb功能活性的C3NeF稳定作用。这些抗独特型抗体对C3NeF的Ka为10(9)升/摩尔,这与C3NeF对其抗原的Ka相当。此外,从MPGN患者中分离出的90%抗独特型抗体和从正常个体中分离出的20%抗独特型抗体类似于Bb,并与C3b以及针对B因子Bb部分的抗体结合。这些抗独特型抗体也类似于C3b,并与针对C3b C3c部分的抗体结合。用后一种形式的抗独特型抗体免疫兔子会导致产生功能活性的C3NeF。这些数据表明,C3NeF抗独特型抗体以两种不同形式存在,具有和不具有C3bBb的内影像,并且可存在于正常个体和MPGN患者中。

相似文献

1
Human anti-idiotypic antibody responses to autoantibody against the alternative pathway C3 convertase.人类针对替代途径C3转化酶自身抗体的抗独特型抗体反应。
Clin Immunol Immunopathol. 1990 Oct;57(1):19-31. doi: 10.1016/0090-1229(90)90019-m.
2
Evidence that production of autoantibody to the alternative pathway C3 convertase is a normal physiologic event.针对替代途径C3转化酶的自身抗体产生是正常生理事件的证据。
J Pediatr. 1990 May;116(5):S103-8. doi: 10.1016/s0022-3476(05)82711-8.
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Autoantibody to the alternative pathway C3/C5 convertase and its anti-idiotypic response. A study in affinity.针对替代途径C3/C5转化酶的自身抗体及其抗独特型反应。亲和力研究。
J Immunol. 1992 Jan 1;148(1):137-41.
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Study of the idiotypic response to autoantibody to the alternative pathway C3/C5 convertase in normal individuals, patients with membranoproliferative glomerulonephritis, and experimental animals.正常个体、膜增生性肾小球肾炎患者及实验动物中针对替代途径C3/C5转化酶自身抗体的独特型反应研究。
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Production of nephritic factor of the alternative complement pathway by Epstein Barr virus-transformed B cell lines derived from a patient with membranoproliferative glomerulonephritis.源自一名膜增生性肾小球肾炎患者的爱泼斯坦-巴尔病毒转化B细胞系产生替代补体途径的肾炎因子。
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Production of IgG and IgM autoantibody to the alternative pathway C3 convertase in normal individuals and patients with membranoproliferative glomerulonephritis.正常个体及膜增生性肾小球肾炎患者体内针对替代途径C3转化酶的IgG和IgM自身抗体的产生。
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Autoantibody to complement neoantigens in membranoproliferative glomerulonephritis.膜增生性肾小球肾炎中针对补体新抗原的自身抗体。
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Human polyclonal and monoclonal IgG and IgM complement 3 nephritic factors: evidence for idiotypic commonality.人多克隆和单克隆IgG及IgM补体3肾炎因子:独特型共同性的证据
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Further evidence for the antibody nature of C3 nephritic factor (C3NeF).C3 肾炎因子(C3NeF)抗体性质的进一步证据。
J Immunol. 1979 Aug;123(2):755-8.
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Selective disappearance of C3NeF IgG autoantibody in the plasma of a patient with membranoproliferative glomerulonephritis following renal transplantation.肾移植后膜增生性肾小球肾炎患者血浆中C3NeF IgG自身抗体的选择性消失。
Nephrol Dial Transplant. 1994;9(7):811-4.

引用本文的文献

1
Protective role of anti-idiotypic antibodies in autoimmunity--lessons for type 1 diabetes.抗独特型抗体在自身免疫中的保护作用——对 1 型糖尿病的启示。
Autoimmunity. 2012 Jun;45(4):320-31. doi: 10.3109/08916934.2012.659299. Epub 2012 Feb 23.
2
Partial lipodystrophy, mesangiocapillary glomerulonephritis, and complement dysregulation. An autoimmune phenomenon.部分脂肪营养不良、系膜毛细血管性肾小球肾炎与补体调节异常。一种自身免疫现象。
Immunol Res. 1998 Aug;18(1):55-60. doi: 10.1007/BF02786513.
3
Significance of C3 nephritic factor (C3NeF) in non-hypocomplementaemic serum with membranoproliferative glomerulonephritis (MPGN).
C3肾炎因子(C3NeF)在非低补体血症性血清伴膜增生性肾小球肾炎(MPGN)中的意义
Clin Exp Immunol. 1992 Sep;89(3):479-84. doi: 10.1111/j.1365-2249.1992.tb06984.x.