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白细胞介素-2融合毒素:皮肤T细胞淋巴瘤的靶向治疗

Interleukin-2 fusion toxin: targeted therapy for cutaneous T cell lymphoma.

作者信息

Foss F M

机构信息

Tufts New England Medical Center, Boston, Massachusetts 02111, USA.

出版信息

Ann N Y Acad Sci. 2001 Sep;941:166-76. doi: 10.1111/j.1749-6632.2001.tb03720.x.

Abstract

The interleukin (IL)-2 receptor has proved an attractive target for T cell-directed therapies. Agents including monoclonal antibodies, single-chain antibody immunoconjugates, radioimmunoconjugates, and, most recently, ligand fusion toxins have demonstrated activity in vitro and in clinical trials in both hematologic malignancies and diseases characterized by proliferation of activated T cells, such as graft-versus-host disease. DAB389IL-2 (ONTAK) is a ligand fusion toxin consisting of the full-length sequence of the IL-2 gene genetically fused to the enzymatically active and translocating domains of diphtheria toxin. DAB389IL-2 and its predecessor, DAB486IL-2, have demonstrated activity in a variety of diseases, including cutaneous T cell lymphoma (CTCL), psoriasis, rheumatoid arthritis, and HIV infection. Further clinical development of IL-2 fusion toxins in CTCL and other hematopoietic malignancies is predicated on identification of the high-affinity IL-2 receptor complex on the malignant cells and on a better understanding of the biological determinants of cytotoxicity of these molecules in vivo.

摘要

白细胞介素(IL)-2受体已被证明是T细胞导向疗法的一个有吸引力的靶点。包括单克隆抗体、单链抗体免疫缀合物、放射免疫缀合物以及最近的配体融合毒素在内的药物,在血液系统恶性肿瘤和以活化T细胞增殖为特征的疾病(如移植物抗宿主病)的体外和临床试验中均显示出活性。DAB389IL-2(昂他克)是一种配体融合毒素,由IL-2基因的全长序列与白喉毒素的酶活性和转位结构域基因融合而成。DAB389IL-2及其前身DAB486IL-2已在多种疾病中显示出活性,包括皮肤T细胞淋巴瘤(CTCL)、银屑病、类风湿性关节炎和HIV感染。IL-2融合毒素在CTCL和其他血液系统恶性肿瘤中的进一步临床开发取决于对恶性细胞上高亲和力IL-2受体复合物的鉴定,以及对这些分子在体内细胞毒性生物学决定因素的更好理解。

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