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输注茴香酰化纤溶酶原-链激酶复合物(APSAC,茴酰化纤溶酶原链激酶激活剂复合物)后出现的药物疹及对链激酶的同型抗体反应。

Drug eruptions and isotypic antibody responses to streptokinase after infusions of anisoylated plasminogen-streptokinase complex (APSAC, anistreplase).

作者信息

Dykewicz M S, McMorrow N K, Davison R, Fintel D J, Zull C C, Rutledge J L

机构信息

Department of Internal Medicine, Saint Louis University School of Medicine, MO 63104-1028, USA.

出版信息

J Allergy Clin Immunol. 1995 May;95(5 Pt 1):1020-8. doi: 10.1016/s0091-6749(95)70103-6.

DOI:10.1016/s0091-6749(95)70103-6
PMID:7751498
Abstract

BACKGROUND

Anisoylated plasminogen-streptokinase complex (APSAC, anistreplase) is a thrombolytic agent (131 kd) used for treatment of myocardial infarction. Like its principal antigenic determinant, streptokinase, APSAC has been reported to cause a variety of allergic reactions.

OBJECTIVE

This study was intended to determine any association between isotypic antibody responses to streptokinase and observed allergic reactions to APSAC.

METHODS

We measured sequential IgM, IgG, IgA, and IgE antistreptokinase serum levels in 21 patients who received APSAC or tissue-type plasminogen activator in a prospective, double-blind study.

RESULTS

Of 11 patients who received APSAC, four had maculopapular rashes and one had urticaria; those with maculopapular rashes had significantly higher rises in serum IgM, IgG, IgA, and IgE antistreptokinase levels. We could not, however, define a temporal relationship between rises in antistreptokinase levels of a particular isotype and the onset of maculopapular rashes. The patient who had urticaria had no antistreptokinase responses but had also received several other potentially causal drugs. None of 10 patients who received tissue-type plasminogen activator had allergic reactions or significant rises in serum antistreptokinase levels.

CONCLUSION

The more vigorous panisotypic antistreptokinase responses observed in patients who received APSAC and had maculopapular rashes may reflect generalized immune system activation that included other immune responses (such as cell-mediated hypersensitivity) that were responsible for these reactions.

摘要

背景

茴香酰化纤溶酶原-链激酶复合物(APSAC,茴酰纤溶酶原链激酶激活剂)是一种用于治疗心肌梗死的溶栓剂(131kd)。与它的主要抗原决定簇链激酶一样,据报道APSAC可引起多种过敏反应。

目的

本研究旨在确定对链激酶的同型抗体反应与观察到的对APSAC的过敏反应之间是否存在关联。

方法

在一项前瞻性双盲研究中,我们检测了21例接受APSAC或组织型纤溶酶原激活剂治疗的患者血清中IgM、IgG、IgA和IgE抗链激酶水平的变化。

结果

11例接受APSAC治疗的患者中,4例出现斑丘疹,1例出现荨麻疹;出现斑丘疹的患者血清中IgM、IgG、IgA和IgE抗链激酶水平升高显著。然而,我们无法确定特定同型抗链激酶水平升高与斑丘疹发作之间的时间关系。出现荨麻疹的患者没有抗链激酶反应,但也接受了其他几种可能引起过敏的药物。10例接受组织型纤溶酶原激活剂治疗的患者均未出现过敏反应,血清抗链激酶水平也未显著升高。

结论

接受APSAC治疗且出现斑丘疹的患者中观察到的更强烈的全同型抗链激酶反应可能反映了全身免疫系统的激活,其中包括导致这些反应的其他免疫反应(如细胞介导的超敏反应)。

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