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本文引用的文献

1
Heritable risk for severe anaphylaxis associated with increased α-tryptase-encoding germline copy number at TPSAB1.与 TPSAB1 中 α-色氨酸酶编码种系拷贝数增加相关的严重过敏反应的遗传风险。
J Allergy Clin Immunol. 2021 Feb;147(2):622-632. doi: 10.1016/j.jaci.2020.06.035. Epub 2020 Jul 24.
2
Mast cells are increased in the small intestinal mucosa of patients with irritable bowel syndrome: A systematic review and meta-analysis.肠易激综合征患者小肠黏膜中的肥大细胞增多:系统评价和荟萃分析。
Neurogastroenterol Motil. 2019 Dec;31(12):e13718. doi: 10.1111/nmo.13718. Epub 2019 Sep 9.
3
AAAAI Mast Cell Disorders Committee Work Group Report: Mast cell activation syndrome (MCAS) diagnosis and management.AAAAI 肥大细胞疾病委员会工作组报告:肥大细胞活化综合征 (MCAS) 的诊断和管理。
J Allergy Clin Immunol. 2019 Oct;144(4):883-896. doi: 10.1016/j.jaci.2019.08.023. Epub 2019 Aug 30.
4
Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia.遗传性 α-胰蛋白酶血症发病机制中天然形成的人 α/β-类胰蛋白酶异四聚体的影响。
J Exp Med. 2019 Oct 7;216(10):2348-2361. doi: 10.1084/jem.20190701. Epub 2019 Jul 23.
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Intestinal Mucosal Mast Cells: Key Modulators of Barrier Function and Homeostasis.肠道黏膜肥大细胞:屏障功能和稳态的关键调节者。
Cells. 2019 Feb 8;8(2):135. doi: 10.3390/cells8020135.
6
Association of Postural Tachycardia Syndrome and Ehlers-Danlos Syndrome with Mast Cell Activation Disorders.体位性心动过速综合征和埃勒斯-当洛综合征与肥大细胞活化障碍的关联。
Immunol Allergy Clin North Am. 2018 Aug;38(3):497-504. doi: 10.1016/j.iac.2018.04.004. Epub 2018 Jun 9.
7
Hereditary Alpha Tryptasemia: Genotyping and Associated Clinical Features.遗传性α-色氨酸血症:基因分型及相关临床特征
Immunol Allergy Clin North Am. 2018 Aug;38(3):483-495. doi: 10.1016/j.iac.2018.04.003. Epub 2018 Jun 9.
8
Are Enterocolic Mucosal Mast Cell Aggregates Clinically Relevant in Patients Without Suspected or Established Systemic Mastocytosis?肠黏膜肥大细胞聚集在无可疑或明确系统性肥大细胞增多症的患者中具有临床意义吗?
Am J Surg Pathol. 2018 Oct;42(10):1390-1395. doi: 10.1097/PAS.0000000000001126.
9
Pathophysiology of irritable bowel syndrome.肠易激综合征的病理生理学。
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10
Pathogenesis and Pathology of Mastocytosis.肥大细胞病的发病机制和病理学。
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遗传性α-胰蛋白酶血症和肥大细胞活化综合征患者的小肠肥大细胞组织学变化特征不同。

Distinct Small Intestine Mast Cell Histologic Changes in Patients With Hereditary Alpha-tryptasemia and Mast Cell Activation Syndrome.

机构信息

Division of Gastroenterology, Hepatology, and Endoscopy.

Departments of Pathology.

出版信息

Am J Surg Pathol. 2021 Jul 1;45(7):997-1004. doi: 10.1097/PAS.0000000000001676.

DOI:10.1097/PAS.0000000000001676
PMID:33481382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8192345/
Abstract

Mast cells (MCs) are important in intestinal homeostasis and pathogen defense but are also implicated in many of the clinical manifestations in disorders such as irritable bowel syndrome. The utility of specific staining for MCs to quantify and phenotype them in intestinal biopsies in patients with gastrointestinal (GI) symptoms is controversial and is not a widely adopted practice. Whether or not intestinal MCs are increased or have a unique phenotype in individuals with hereditary alpha-tryptasemia (HαT), who have extra copies of the MC tryptase gene TPSAB1 and typically elevated baseline serum tryptase levels >8 ng/mL is not known. We examined the duodenal biopsies of 17 patients with HαT and compared them to 15 patients with mast cell activation syndrome who had baseline serum tryptases <8 ng/mL (MCAS-NT) and 12 GI-controls. We determined that the HαT subjects had increased MCs in the duodenum compared with MCAS-NT and GI-controls (median=30.0; interquartile range [IQR]: 20.0 to 40.0 vs. median=15.0; IQR: 5.00 to 20.0; P=0.013 and median=15.0; IQR: 13.8 to 20.0; P=0.004, respectively). These MCs were significantly found in clusters (<15 MCs) and were located throughout the mucosa and submucosa including the superficial villi compared with MCAS-NT and GI-control patients. Spindle-shaped MCs were observed in all groups including controls. These data demonstrate that HαT is associated with increased small intestinal MCs that may contribute to the prevalent GI manifestations observed among individuals with this genetic trait.

摘要

肥大细胞(MCs)在肠道稳态和病原体防御中很重要,但也与许多疾病的临床表现有关,如肠易激综合征。在有胃肠道(GI)症状的患者的肠道活检中,使用特定的染色方法来定量和表型分析 MCs 的方法是否有用存在争议,并且尚未被广泛采用。在遗传性α-胰蛋白酶血症(HαT)患者中,肠道 MC 是增加还是具有独特表型尚不清楚,这些患者的 MC 胰蛋白酶基因 TPSAB1 有额外的拷贝,并且基线血清胰蛋白酶水平通常>8ng/mL。我们检查了 17 例 HαT 患者的十二指肠活检,并将其与 15 例基线血清胰蛋白酶<8ng/mL 的肥大细胞活化综合征(MCAS-NT)患者和 12 例 GI 对照组进行了比较。我们发现,与 MCAS-NT 和 GI 对照组相比,HαT 患者的十二指肠 MC 增加(中位数=30.0;四分位距 [IQR]:20.0 至 40.0 比中位数=15.0;IQR:5.00 至 20.0;P=0.013 和中位数=15.0;IQR:13.8 至 20.0;P=0.004)。这些 MC 主要位于黏膜和黏膜下层,包括浅层绒毛,呈簇状(<15 个 MC),与 MCAS-NT 和 GI 对照组患者相比,MC 明显增加。在所有组包括对照组中均观察到梭形 MC。这些数据表明,HαT 与小肠 MC 增加有关,这可能导致具有这种遗传特征的个体中常见的 GI 表现。

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