Pathogenesis of autoimmune and hereditary pancreatitis with a focus on neutrophil granulocytes and neutrophil serine proteases

Lukas Zierke, Marcel Gischke, Q. Tran, A. Aghdassi
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Abstract

Hereditary and autoimmune pancreatitis are two rare forms of inflammatory pancreatic disorders. Both share similarities with acute, acute recurrent, and chronic pancreatitis. Regarding their pathogenesis, the premature activation of the digestive protease trypsinogen and the infiltration of inflammatory cells such as polymorphonuclear leukocytes and macrophages into the pancreas are highly relevant and can reciprocally amplify inflammation. Neutrophil serine proteases are the main components of neutrophil granulocytes and have different pro-inflammatory effects in many diseases. However, their role in pancreatitis is still limited. This section focuses on known findings regarding the role of this group of enzymes in hereditary and autoimmune pancreatitis.
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自身免疫性和遗传性胰腺炎的发病机制,重点是中性粒细胞和中性粒细胞丝氨酸蛋白酶
遗传性和自身免疫性胰腺炎是两种罕见的炎症性胰腺疾病。两者与急性、急性复发性和慢性胰腺炎有相似之处。关于其发病机制,消化蛋白酶胰蛋白酶原的过早激活与胰腺内多形核白细胞、巨噬细胞等炎症细胞的浸润高度相关,并可相互放大炎症。中性粒细胞丝氨酸蛋白酶是中性粒细胞的主要成分,在多种疾病中具有不同的促炎作用。然而,它们在胰腺炎中的作用仍然有限。本节的重点是关于这组酶在遗传性和自身免疫性胰腺炎中的作用的已知发现。
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