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非感染性混合性冷球蛋白血症作为编码外被体亚基α基因变异的一种新临床表现:两例成年姐妹的病例报告

Non-infectious mixed cryoglobulinemia as a new clinical presentation of mutation in the gene encoding coatomer subunit alpha: a case report of two adult sisters.

作者信息

Leśniak Ksymena, Płoski Rafał, Rydzanicz Małgorzata, Rymarz Aleksandra, Lubas Arkadiusz, Syryło Tomasz, Niemczyk Stanisław

机构信息

Department of Internal Diseases, Nephrology and Dialysis, Military Institute of Medicine-National Research Institute, Warsaw, Poland.

Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.

出版信息

Front Immunol. 2024 Nov 15;15:1450048. doi: 10.3389/fimmu.2024.1450048. eCollection 2024.

DOI:10.3389/fimmu.2024.1450048
PMID:39620212
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11604590/
Abstract

Cryoglobulinemia is a rare disease characterized by the presence of cryoglobulins in the blood serum. It is usually caused by autoimmune, lymphoproliferative, or infectious factors. The pathogenesis of cryoglobulinemia is not well understood, therefore, genetic testing is very important. We present the case of two adult sisters with different clinical phenotypes of non-infectious cryoglobulinemic vasculitis associated with a rare genetic variant [(Hg38) 1:160323529 C>G, NP_004362.2:p.(Gly203Ala)]. One of the sisters suffered from essential mixed cryoglobulinemia, while the other suffered from cryoglobulinemia associated with systemic connective tissue disease. In both cases, genetic tests revealed a variant in the COPA gene, encoding coatomer subunit alpha. Mutations in the COPA gene are associated with COPA syndrome, an autoimmune interstitial lung, joint, and kidney monogenic disease, found mainly in children. Only 15 pathogenic COPA variants have been reported thus far which suggests that the full spectrum of disease manifestations remains unknown. Ours is the first report of the association of the COPA gene with non-infectious cryoglobulinemic vasculitis in adults. This unexpected finding may direct research into the pathogenesis of cryoglobulinemia and new treatment strategies for this rare disease.

摘要

冷球蛋白血症是一种罕见疾病,其特征是血清中存在冷球蛋白。它通常由自身免疫、淋巴增殖或感染因素引起。冷球蛋白血症的发病机制尚不完全清楚,因此基因检测非常重要。我们报告了两例成年姐妹患有与一种罕见基因变异[(Hg38) 1:160323529 C>G, NP_004362.2:p.(Gly203Ala)]相关的非感染性冷球蛋白血症性血管炎的不同临床表型的病例。其中一名姐妹患有原发性混合性冷球蛋白血症,而另一名姐妹患有与系统性结缔组织病相关的冷球蛋白血症。在这两个病例中,基因检测均显示编码外被体亚基α的COPA基因存在变异。COPA基因突变与COPA综合征相关,这是一种主要在儿童中发现的自身免疫性间质性肺、关节和肾脏单基因疾病。迄今为止,仅报道了15种致病性COPA变异,这表明疾病表现的全貌仍不清楚。我们的研究是首次报道COPA基因与成人非感染性冷球蛋白血症性血管炎的关联。这一意外发现可能会引导对冷球蛋白血症发病机制的研究以及针对这种罕见疾病的新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/367de4a7569a/fimmu-15-1450048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/fd9130de43ca/fimmu-15-1450048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/e8d13f62d401/fimmu-15-1450048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/367de4a7569a/fimmu-15-1450048-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/fd9130de43ca/fimmu-15-1450048-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/e8d13f62d401/fimmu-15-1450048-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae34/11604590/367de4a7569a/fimmu-15-1450048-g003.jpg

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本文引用的文献

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Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment.Genebe.net:ACMG 变异致病性标准自动分配的实施与验证
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COPA syndrome caused by a novel p.Arg227Cys COPA gene variant.由新型 COPA 基因变异 p.Arg227Cys 引起的 COPA 综合征。
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Imaging findings of COPA Syndrome.COPA 综合征的影像学表现。
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The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.2022 年更新的人类先天性免疫缺陷疾病表型分类 IUIS
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A Novel Mutation c.841C>T in COPA Syndrome of an 11-Year-Old Boy: A Case Report and Short Literature Review.一名11岁男孩COPA综合征中的新型突变c.841C>T:病例报告及文献综述
Front Pediatr. 2021 Nov 24;9:773112. doi: 10.3389/fped.2021.773112. eCollection 2021.
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A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathy.一个反复出现的新生变异支持 KCNC2 参与发育性和癫痫性脑病的发病机制。
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