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1
A novel mutant gammac chain from a patient with typical phenotype of X-linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL-2 and IL-4 receptor action.一名患有典型X连锁重症联合免疫缺陷(SCID)表型患者的新型γ链突变体对介导白细胞介素-2(IL-2)和白细胞介素-4(IL-4)受体作用具有部分信号传导功能。
Clin Exp Immunol. 1999 Feb;115(2):356-61. doi: 10.1046/j.1365-2249.1999.00792.x.
2
Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiency.用于诊断T-B+重症联合免疫缺陷的基于蛋白质的快速检测方法。
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Functional role of interleukin-4 (IL-4) and IL-7 in the development of X-linked severe combined immunodeficiency.
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Cytokine. 2010 Feb;49(2):221-8. doi: 10.1016/j.cyto.2009.09.009. Epub 2009 Nov 3.
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A novel splice-site mutation in the common gamma chain (gammac) gene IL2RG results in X-linked severe combined immunodeficiency with an atypical NK+ phenotype.常见γ链(γc)基因IL2RG中的一种新型剪接位点突变导致具有非典型NK+表型的X连锁重症联合免疫缺陷。
Hum Mutat. 2004 May;23(5):522-3. doi: 10.1002/humu.9235.
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Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid development.一名重症联合免疫缺陷病(SCID)患者中Jak3的突变:Jak3在淋巴细胞发育中的关键作用
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In vitro correction of JAK3-deficient severe combined immunodeficiency by retroviral-mediated gene transduction.通过逆转录病毒介导的基因转导对JAK3缺陷型重症联合免疫缺陷进行体外校正。
J Exp Med. 1996 Jun 1;183(6):2687-92. doi: 10.1084/jem.183.6.2687.
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Mutations in the gene for the common gamma chain (gammac) in X-linked severe combined immunodeficiency.X连锁重症联合免疫缺陷中常见γ链(γc)基因的突变。
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X-linked SCID and other defects of cytokine pathways.X连锁重症联合免疫缺陷病及其他细胞因子信号通路缺陷
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hypomorphic mutation: identification of a novel pathogenic mutation in exon 8 and a review of the literature.低表达突变:外显子8中一个新的致病突变的鉴定及文献综述
Allergy Asthma Clin Immunol. 2019 Jan 5;15:2. doi: 10.1186/s13223-018-0317-y. eCollection 2019.
2
A novel deletion mutation in IL2RG gene results in X-linked severe combined immunodeficiency with an atypical phenotype.IL2RG基因中的一种新型缺失突变导致具有非典型表型的X连锁重症联合免疫缺陷。
Immunogenetics. 2017 Jan;69(1):29-38. doi: 10.1007/s00251-016-0949-3. Epub 2016 Aug 26.
3
Interleukin-2 signaling and inherited immunodeficiency.白细胞介素-2信号传导与遗传性免疫缺陷
Am J Hum Genet. 1999 Aug;65(2):287-93. doi: 10.1086/302518.

本文引用的文献

1
Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants.人类重症联合免疫缺陷:108例婴儿的遗传、表型和功能多样性
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2
IL2RGbase: a database of gamma c-chain defects causing human X-SCID.IL2RGbase:一个关于导致人类X连锁重症联合免疫缺陷的γ链缺陷的数据库。
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Modulation of hematopoiesis in mice with a truncated mutant of the interleukin-2 receptor gamma chain.用白细胞介素-2受体γ链截短突变体对小鼠造血功能的调节
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Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans.白细胞介素-2受体γ链突变导致人类X连锁重症联合免疫缺陷。
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Interleukin-2 receptor gamma chain: a functional component of the interleukin-4 receptor.白细胞介素-2受体γ链:白细胞介素-4受体的功能组分。
Science. 1993 Dec 17;262(5141):1880-3. doi: 10.1126/science.8266078.
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Interleukin-2 receptor gamma chain: a functional component of the interleukin-7 receptor.白细胞介素-2受体γ链:白细胞介素-7受体的功能成分。
Science. 1993 Dec 17;262(5141):1877-80. doi: 10.1126/science.8266077.
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Sharing of the interleukin-2 (IL-2) receptor gamma chain between receptors for IL-2 and IL-4.白细胞介素-2(IL-2)受体γ链在IL-2和IL-4受体之间的共用。
Science. 1993 Dec 17;262(5141):1874-7. doi: 10.1126/science.8266076.
9
Functional participation of the IL-2 receptor gamma chain in IL-7 receptor complexes.白细胞介素-2受体γ链在白细胞介素-7受体复合物中的功能参与。
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Utilization of the beta and gamma chains of the IL-2 receptor by the novel cytokine IL-15.新型细胞因子IL-15对IL-2受体β链和γ链的利用
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一名患有典型X连锁重症联合免疫缺陷(SCID)表型患者的新型γ链突变体对介导白细胞介素-2(IL-2)和白细胞介素-4(IL-4)受体作用具有部分信号传导功能。

A novel mutant gammac chain from a patient with typical phenotype of X-linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL-2 and IL-4 receptor action.

作者信息

Kumaki S, Ochs H D, Kuropatwinski K K, Konno T, Timour M S, Cosman D, Baumann H

机构信息

Department of Pediatrics, University of Washington, Seattle, WA, USA.

出版信息

Clin Exp Immunol. 1999 Feb;115(2):356-61. doi: 10.1046/j.1365-2249.1999.00792.x.

DOI:10.1046/j.1365-2249.1999.00792.x
PMID:9933465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905160/
Abstract

Mutations of the common gamma (gammac) chain result in X-linked SCID (X-SCID), which is characterized by the reduction in number or absence of peripheral blood T cells and natural killer (NK) cells, with retention of normal numbers of B cells. In the present study we describe a novel mutant gammac chain of an X-SCID patient with a typical X-SCID phenotype. This mutant receptor subunit is able to associate with Jak3 to transduce a weak signal. The Jak3-specific action is demonstrated by the induction of gene expression through the haematopoietin receptor response element (HRRE) by IL-2 and IL-4 in the experimental model of transiently transfected hepatoma cells over-expressing Jak3. This result suggests that a threshold in the gammac-Jak3 interaction determines the X-SCID phenotype.

摘要

共同γ(γc)链的突变导致X连锁重症联合免疫缺陷病(X-SCID),其特征是外周血T细胞和自然杀伤(NK)细胞数量减少或缺失,而B细胞数量正常。在本研究中,我们描述了一名具有典型X-SCID表型的X-SCID患者的新型突变γc链。这种突变受体亚基能够与Jak3结合以转导微弱信号。在过表达Jak3的瞬时转染肝癌细胞实验模型中,IL-2和IL-4通过造血受体反应元件(HRRE)诱导基因表达,证明了Jak3的特异性作用。该结果表明γc-Jak3相互作用中的一个阈值决定了X-SCID表型。