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X连锁低丙种球蛋白血症中的C1酯酶抑制剂缺乏:一种在肌内注射丙种球蛋白后引发类过敏反应的异常情况。

C1 esterase inhibitor deficiency in X-linked hypogammaglobulinaemia: an anomaly fostering anaphylactoid reactions following intramuscular gammaglobulin administration.

作者信息

Pollack S, Cunningham-Rundles C, Good R A, Day N K

出版信息

Postgrad Med J. 1986 Oct;62(732):939-42. doi: 10.1136/pgmj.62.732.939.

DOI:10.1136/pgmj.62.732.939
PMID:2430274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2419044/
Abstract

A patient with apparent X-linked agammaglobulinaemia was found to be inordinately susceptible to anaphylactoid reactions to intramuscular injections of gammaglobulin. The patient was found also to have low levels of C1 esterase inhibitor (C1 INH). The possibility that the C1 INH deficiency and in this patient, whether genetic or acquired, fostered the susceptibility to the production of anaphylactoid reactions after gammaglobulin injections urges further studies of the association of C1 INH deficiency and anaphylactoid reactions to gammaglobulin injections. The possibility that C1 INH levels like C1q levels may be low in hypogammaglobulinaemic patients as a consequence of increased catabolism of this regulator of the complement system when IgG levels are low is considered.

摘要

一名明显患有X连锁无丙种球蛋白血症的患者被发现对肌肉注射丙种球蛋白产生类过敏反应异常敏感。该患者还被发现C1酯酶抑制剂(C1 INH)水平较低。C1 INH缺乏,无论在该患者中是遗传性还是获得性的,是否会促使其在注射丙种球蛋白后易产生类过敏反应,这一可能性促使人们进一步研究C1 INH缺乏与丙种球蛋白注射后类过敏反应之间的关联。有人认为,由于当IgG水平较低时补体系统调节因子的分解代谢增加,低丙种球蛋白血症患者的C1 INH水平可能与C1q水平一样较低。

相似文献

1
C1 esterase inhibitor deficiency in X-linked hypogammaglobulinaemia: an anomaly fostering anaphylactoid reactions following intramuscular gammaglobulin administration.X连锁低丙种球蛋白血症中的C1酯酶抑制剂缺乏:一种在肌内注射丙种球蛋白后引发类过敏反应的异常情况。
Postgrad Med J. 1986 Oct;62(732):939-42. doi: 10.1136/pgmj.62.732.939.
2
Acute consumption of C1 inhibitor in a patient with acquired C1-inhibitor deficiency syndrome.获得性C1抑制物缺乏综合征患者急性使用C1抑制物。
J Allergy Clin Immunol. 1991 Dec;88(6):908-18. doi: 10.1016/0091-6749(91)90248-m.
3
The long term treatment of childhood hypogammaglobulinaemia in Melbourne with intravenous gammaglobulin, 1972-1985.1972年至1985年墨尔本地区采用静脉注射丙种球蛋白对儿童低丙种球蛋白血症进行的长期治疗
Dev Biol Stand. 1987;67:273-80.
4
Home treatment of hypogammaglobulinaemia with subcutaneous gammaglobulin by rapid infusion.皮下注射球蛋白快速输注在家中治疗低丙种球蛋白血症
Lancet. 1991 Jul 20;338(8760):162-6. doi: 10.1016/0140-6736(91)90147-h.
5
[Acquired C1 esterase inhibitor deficiency and lymphoproliferative syndromes].
Rev Med Interne. 1985 Jun;6(3):266-71. doi: 10.1016/s0248-8663(85)80116-8.
6
[Treatment of primary immunodeficiencies with intravenous gamma globulin].[静脉注射丙种球蛋白治疗原发性免疫缺陷病]
An Esp Pediatr. 1987 Dec;27(6):411-5.
7
Angioedema due to acquired C1-esterase inhibitor deficiency in a patient with Helicobacter pylori infection.一名幽门螺杆菌感染患者因获得性C1酯酶抑制剂缺乏症导致血管性水肿。
Z Gastroenterol. 1999 Jun;37(6):513-8.
8
Acquired C1-inhibitor deficiency in essential cryoglobulinemia and macrocryoglobulinemia.
Acta Haematol. 1978;59(5):277-84. doi: 10.1159/000207773.
9
[The course of acquired C 1 esterase inhibitor deficiency in lymphoproliferative syndrome].[淋巴细胞增殖综合征中获得性C1酯酶抑制剂缺乏症的病程]
Ann Med Interne (Paris). 1988;139(7):488-90.
10
Hereditary and acquired deficiencies of C1 inhibitor.C1抑制剂的遗传性和获得性缺陷
Immunodefic Rev. 1989;1(3):207-26.

本文引用的文献

1
Adverse reactions in selected patients following intravenous infusions of gamma globulin.静脉输注丙种球蛋白后部分患者出现的不良反应。
Am J Med. 1984 Mar 30;76(3A):25-32. doi: 10.1016/0002-9343(84)90316-4.
2
Decreased C'-1q protein concentration and agglutinating activity in agammaglobulinaemia syndromes: an inborn error reflected in the complement system.无丙种球蛋白血症综合征中C'-1q蛋白浓度降低及凝集活性降低:补体系统中反映出的一种先天性缺陷。
Clin Exp Immunol. 1968 Jun;3(5):437-45.
3
Metabolism of human C1q. Studies in hypogammaglobulinemia, myeloma, and systemic lupus erythematosus.人C1q的代谢。低丙种球蛋白血症、骨髓瘤及系统性红斑狼疮的研究。
J Clin Invest. 1972 Apr;51(4):868-75. doi: 10.1172/JCI106881.
4
Reconstitution of Clq after bone marrow transplantation in patients with severe combined immunodeficiency.
Clin Immunol Immunopathol. 1973 Nov;2(1):28-35. doi: 10.1016/0090-1229(73)90033-0.
5
Hereditary angioedema: the clinical syndrome and its management.遗传性血管性水肿:临床综合征及其管理
Ann Intern Med. 1976 May;84(5):580-93. doi: 10.7326/0003-4819-84-5-580.
6
Evidence for immune complexes involving anti-lymphocyte antibodies associated with hypocomplementaemia in chronic lymphocytic leukaemia (CLL).慢性淋巴细胞白血病(CLL)中存在涉及抗淋巴细胞抗体的免疫复合物与补体血症相关的证据。
Clin Exp Immunol. 1976 Nov;26(2):189-95.
7
The Raji cell radioimmune assay for detecting immune complexes in human sera.用于检测人血清中免疫复合物的拉吉细胞放射免疫测定法。
J Clin Invest. 1976 Jan;57(1):169-82. doi: 10.1172/JCI108257.
8
Reduced concentrations of the first component of complement in hypotammaglobulinemia: correction of infusion of gamma-globulin.
Clin Immunol Immunopathol. 1978 Mar;9(3):350-5. doi: 10.1016/0090-1229(78)90106-x.