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小鼠严重联合免疫缺陷(SCID)。病理学、重建、肿瘤

Severe combined immunodeficiency (SCID) in the mouse. Pathology, reconstitution, neoplasms.

作者信息

Custer R P, Bosma G C, Bosma M J

出版信息

Am J Pathol. 1985 Sep;120(3):464-77.

Abstract

Histologic findings in mice with severe combined immunodeficiency (SCID) were remarkably uniform, consisting of lymphopenia, a rudimentary thymic medulla without cortex, relatively empty splenic follicles and lymph nodes, and undeveloped bronchial and gastrointestinal lymphocytic foci. Fluorescence-activated cell sorter studies revealed a few T cells (apparently nonfunctional) in thymus and spleen; interestingly, these cells seemed highly disposed to neoplasia, because thymic T-cell lymphomas were observed in 41 of 269 mice. No pre-B or B cells could be identified. Cells of the myeloid lineage appeared normal. Reconstitution of lymphoid tissues was achieved after intravenous injection of histocompatible bone marrow cells.

摘要

严重联合免疫缺陷(SCID)小鼠的组织学表现非常一致,包括淋巴细胞减少、无皮质的原始胸腺髓质、相对空虚的脾滤泡和淋巴结,以及未发育的支气管和胃肠道淋巴细胞灶。荧光激活细胞分选研究显示,胸腺和脾脏中有少量T细胞(显然无功能);有趣的是,这些细胞似乎极易发生肿瘤形成,因为在269只小鼠中有41只观察到胸腺T细胞淋巴瘤。未发现前B细胞或B细胞。髓系细胞系的细胞看起来正常。静脉注射组织相容性骨髓细胞后,淋巴组织得以重建。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b9/1887984/3251ca93b3ee/amjpathol00168-0146-a.jpg

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