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中性粒细胞和单核细胞上凯尔血型系统的抗原:它们与慢性肉芽肿病的关系。

Antigens of the Kell blood group system on neutrophils and monocytes: their relation to chronic granulomatous disease.

作者信息

Marsh W L, Uretsky S C, Douglas S D

出版信息

J Pediatr. 1975 Dec;87(6 Pt 2):1117-20. doi: 10.1016/s0022-3476(75)80124-7.

DOI:10.1016/s0022-3476(75)80124-7
PMID:52702
Abstract

KX, an antigen related to the Kell blood group system, is present in trace amounts on normal red cells and is strongly active on the neutrophils of all of 50 persons thus far tested. Normal circulating monocytes are now shown to also bear KX determinants. Absence of neutrophil KX has been associated with all of three previously tested patients with chronic granulomatous disease. In this study two male siblings with CGD also have been shown to have KX negative leukocytes, and white blood cells from their heterozygous mother were found to have a reduced competency to absorb anti-KX. Five CGD boys are known to lack KX; the probability of this occurring by chance is greater 10(-6).

摘要

KX是一种与凯尔血型系统相关的抗原,在正常红细胞上含量微量,而在迄今检测的所有50人的中性粒细胞上活性很强。现已证明正常循环单核细胞也带有KX决定簇。三名先前检测的慢性肉芽肿病患者的中性粒细胞均缺乏KX。在本研究中,两名患有慢性肉芽肿病的男性同胞也被证明白细胞KX阴性,并且发现他们杂合子母亲的白细胞吸收抗KX的能力降低。已知五名患有慢性肉芽肿病的男孩缺乏KX;这种情况偶然发生的概率大于10的负6次方。

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1
Antigens of the Kell blood group system on neutrophils and monocytes: their relation to chronic granulomatous disease.中性粒细胞和单核细胞上凯尔血型系统的抗原:它们与慢性肉芽肿病的关系。
J Pediatr. 1975 Dec;87(6 Pt 2):1117-20. doi: 10.1016/s0022-3476(75)80124-7.
2
Chronic granulomatous disease and the Kell blood groups.慢性肉芽肿病与凯尔血型系统
Br J Haematol. 1975 Feb;29(2):247-62. doi: 10.1111/j.1365-2141.1975.tb01819.x.
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The Kell blood group, Kx antigen, and chronic granulomatous disease.凯尔血型、Kx抗原与慢性肉芽肿病。
Mayo Clin Proc. 1977 Mar;52(3):150-2.
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Kx antigen, the McLeod phenotype, and chronic granulomatous disease: further studies.Kx抗原、麦克劳德表型与慢性肉芽肿病:进一步研究
Vox Sang. 1976 Nov;31(5):356-62. doi: 10.1111/j.1423-0410.1976.tb04659.x.
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Chronic granulomatous disease and the Mcleod phenotype. Successful treatment of infection with granulocyte transfusions resulting in subsequent hemolytic transfusion reaction.慢性肉芽肿病与麦克劳德表型。粒细胞输注成功治疗感染后发生溶血性输血反应。
Mayo Clin Proc. 1977 Mar;52(3):153-6.
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Auto analyzer determination of red cell Kell phenotypes in patients with chronic granulomatous disease (CGD) and heterozygous carriers.自动分析仪测定慢性肉芽肿病(CGD)患者及杂合子携带者的红细胞凯尔血型表型。
Br J Haematol. 1978 Jul;39(3):351-5. doi: 10.1111/j.1365-2141.1978.tb01107.x.
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First example of anti-Kx in a person with the McLeod phenotype and without chronic granulomatous disease.首例在具有麦克劳德表型且无慢性肉芽肿病的个体中发现抗Kx的情况。
Transfusion. 2000 Nov;40(11):1371-5. doi: 10.1046/j.1537-2995.2000.40111371.x.
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Human granulocytes lack red cell Kx antigen.人类粒细胞缺乏红细胞Kx抗原。
Br J Haematol. 1986 Apr;62(4):747-55. doi: 10.1111/j.1365-2141.1986.tb04098.x.
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Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and Km.对一名无慢性肉芽肿病、有抗Kx和Km抗体的McLeod表型患者的输血支持。
Vox Sang. 2008 Apr;94(3):216-220. doi: 10.1111/j.1423-0410.2007.01021.x. Epub 2007 Dec 18.
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Chronic granulomatous disease, Kx negative neutrophils and linkage with Xg.慢性肉芽肿病、Kx阴性中性粒细胞与Xg的连锁关系
Adv Exp Med Biol. 1982;141:655-8. doi: 10.1007/978-1-4684-8088-7_65.

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