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Updated: Jun 4, 2025

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载体化人类抗体介导的抗乙素基因疗法

Maria Gioulvanidou1, Selenay Sarklioglu1, Xinlei Chen2

  • 1Department of Genetic Medicine, Weill Cornell Medical College, New York, New York, USA.

Human gene therapy
|December 26, 2024
PubMed
概括

使用腺相关病毒 (AAV) 的基因疗法产生了一种新型抗体,以向埃索诺菲尔. 这种方法显示出一种一次性治疗的潜力,以抑制慢性过敏氨基酸性过敏氨基酸水平.

关键词:
腺相关病毒的病毒.埃索诺菲利亚 (eosinophilia) 是一种基因治疗的基因疗法

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Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
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