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一个CD45小基因可恢复CD45缺陷小鼠中受调控的异构体表达及免疫功能:对人类CD45缺失型重症联合免疫缺陷的治疗意义。

A CD45 minigene restores regulated isoform expression and immune function in CD45-deficient mice: therapeutic implications for human CD45-null severe combined immunodeficiency.

作者信息

Virts Elizabeth L, Diago Oscar, Raschke William C

机构信息

Sidney Kimmel Cancer Center, San Diego, CA, USA.

出版信息

Blood. 2003 Feb 1;101(3):849-55. doi: 10.1182/blood-2002-07-1969. Epub 2002 Sep 19.

Abstract

Transgenic mice have been generated that carry a CD45 minigene under control of the human leukocyte function-associated antigen (LFA-1, CD11a) promoter. CD45-null mice carrying the transgene exhibit the lymphocyte lineage-specific isoform expression patterns of wild-type mice. Furthermore, these mice have normal thymocyte development and peripheral T-cell numbers. The proliferative ability of T cells in response to mitogens and antigen also is regained, as is B-cell responsiveness to anti-IgM. The antibody response to antigen is also restored and is similar to that of normal mice. Therefore, introduction of a functional CD45 minigene is sufficient to overcome the principal severe combined immunodeficiency (SCID)-associated defects and represents a potential route to a gene therapy for human CD45-deficent SCID.

摘要

已经培育出转基因小鼠,其携带在人类白细胞功能相关抗原(LFA-1,CD11a)启动子控制下的CD45小基因。携带该转基因的CD45基因敲除小鼠表现出野生型小鼠的淋巴细胞谱系特异性同工型表达模式。此外,这些小鼠具有正常的胸腺细胞发育和外周T细胞数量。T细胞对有丝分裂原和抗原的增殖能力也得以恢复,B细胞对抗IgM的反应性也是如此。对抗原的抗体反应也得以恢复,且与正常小鼠相似。因此,引入功能性CD45小基因足以克服主要的严重联合免疫缺陷(SCID)相关缺陷,代表了一种针对人类CD45缺陷型SCID的基因治疗潜在途径。

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