Article ; Online: New therapeutic strategies based on biasing IL-2 mutants for cancers and autoimmune diseases.
International immunopharmacology
2022 Volume 110, Page(s) 108935
Abstract: Interleukin-2 (IL-2) is an immunomodulatory multifunctional cytokine. High-dose IL-2 was first approved by the U.S. Food and Drug Administration (FDA) in the 1990s for the treatment of metastatic renal cell carcinoma and metastatic melanoma. However, the ...
Abstract | Interleukin-2 (IL-2) is an immunomodulatory multifunctional cytokine. High-dose IL-2 was first approved by the U.S. Food and Drug Administration (FDA) in the 1990s for the treatment of metastatic renal cell carcinoma and metastatic melanoma. However, the short half-life of IL-2 and its toxicity caused by high-dose IL-2 limit the clinical use of IL-2. Recently, the development of cell-type-selective engineered IL-2 products become a hot research filed, mainly because IL-2 stimulates both regulatory T cells (Treg) and effector T cells (Teff) in vivo. The selective effect of IL-2 on Treg and Teff can be improved by designing biased IL-2 mutants, which showed reduced toxicity while being more effective in stimulating anti-tumor effector immunity or ameliorating autoimmune diseases. In this review we summarize the biological properties of IL-2 mutants reported so far. The design process and principle of IL-2 mutants, IL-2 mutant antibody complexes and IL-2 fusion proteins were discussed, which provided research basis for the design and application of IL-2 mutants in the future. |
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MeSH term(s) | Autoimmune Diseases/drug therapy ; Autoimmune Diseases/genetics ; Carcinoma, Renal Cell ; Humans ; Interleukin-2/genetics ; Interleukin-2/metabolism ; Interleukin-2/therapeutic use ; Kidney Neoplasms ; T-Lymphocytes, Regulatory |
Chemical Substances | Interleukin-2 |
Language | English |
Publishing date | 2022-06-19 |
Publishing country | Netherlands |
Document type | Journal Article ; Review |
ZDB-ID | 2043785-7 |
ISSN | 1878-1705 ; 1567-5769 |
ISSN (online) | 1878-1705 |
ISSN | 1567-5769 |
DOI | 10.1016/j.intimp.2022.108935 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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