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髓过氧化物酶缺乏症。

Myeloperoxidase deficiency.

作者信息

Nauseef W M

机构信息

Division of Infectious Disease, University of Iowa, Iowa City.

出版信息

Hematol Oncol Clin North Am. 1988 Mar;2(1):135-58.

PMID:2831185
Abstract

MPO activity is critical for optimal microbicidal activity of normal PMNs. In the absence of MPO, auxiliary mechanisms protect most MPO-deficient hosts from clinically significant sequelae, except for some persons with diabetes mellitus who suffer severe candidal disease. However, given our limited knowledge of the clinical impact of MPO deficiency, histochemical staining of peripheral blood smears or MPO activity of isolated leukocytes should be assessed in patients with unexplained fungal disease or with suspected impaired host defenses. Recently isolated cDNA probes provide important tools for dissecting the molecular and cell biology underlying hereditary MPO deficiency and the link between MPO gene expression and myeloid differentiation.

摘要

髓过氧化物酶(MPO)活性对于正常中性粒细胞的最佳杀菌活性至关重要。在缺乏MPO的情况下,辅助机制可保护大多数MPO缺乏的宿主免于出现具有临床意义的后遗症,但患有严重念珠菌病的糖尿病患者除外。然而,鉴于我们对MPO缺乏的临床影响了解有限,对于患有不明原因的真菌病或疑似宿主防御功能受损的患者,应评估外周血涂片的组织化学染色或分离白细胞的MPO活性。最近分离出的cDNA探针为剖析遗传性MPO缺乏的分子和细胞生物学以及MPO基因表达与髓系分化之间的联系提供了重要工具。

相似文献

1
Myeloperoxidase deficiency.髓过氧化物酶缺乏症。
Hematol Oncol Clin North Am. 1988 Mar;2(1):135-58.
2
Aberrant restriction endonuclease digests of DNA from subjects with hereditary myeloperoxidase deficiency.
Blood. 1989 Jan;73(1):290-5.
3
Insights into myeloperoxidase biosynthesis from its inherited deficiency.从髓过氧化物酶遗传性缺乏症看其生物合成机制
J Mol Med (Berl). 1998 Sep;76(10):661-8. doi: 10.1007/s001090050265.
4
Pattern of inheritance in hereditary myeloperoxidase deficiency associated with the R569W missense mutation.与R569W错义突变相关的遗传性髓过氧化物酶缺乏症的遗传模式。
J Leukoc Biol. 1998 Feb;63(2):264-9. doi: 10.1002/jlb.63.2.264.
5
Biosynthesis and processing of myeloperoxidase--a marker for myeloid cell differentiation.髓过氧化物酶的生物合成与加工——髓样细胞分化的标志物
Eur J Haematol. 1988 Feb;40(2):97-110. doi: 10.1111/j.1600-0609.1988.tb00805.x.
6
Quality control in the endoplasmic reticulum: lessons from hereditary myeloperoxidase deficiency.内质网中的质量控制:来自遗传性髓过氧化物酶缺乏症的教训。
J Lab Clin Med. 1999 Sep;134(3):215-21. doi: 10.1016/s0022-2143(99)90200-7.
7
Evidence for a pretranslational defect in hereditary and acquired myeloperoxidase deficiency.
Blood. 1989 May 15;73(7):1980-6.
8
Biochemical and immunologic analysis of hereditary myeloperoxidase deficiency.遗传性髓过氧化物酶缺乏症的生化与免疫学分析
J Clin Invest. 1983 May;71(5):1297-307. doi: 10.1172/jci110880.
9
Effect of the R569W missense mutation on the biosynthesis of myeloperoxidase.R569W错义突变对髓过氧化物酶生物合成的影响。
J Biol Chem. 1996 Apr 19;271(16):9546-9. doi: 10.1074/jbc.271.16.9546.
10
Myeloperoxidase deficiency. Increased sensitivity for immunocytochemical compared to cytochemical detection of enzyme.髓过氧化物酶缺乏症。与酶的细胞化学检测相比,免疫细胞化学检测的敏感性增加。
Arch Pathol Lab Med. 1985 Nov;109(11):1005-6.

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