![]() Mitazalimab structure
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Common Name | Mitazalimab | ||
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CAS Number | 2055640-86-1 | Molecular Weight | N/A | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | N/A | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of MitazalimabMitazalimab (ADC-1013; JNJ-64457107) is FcγR-dependent CD40 agonist with tumor-directed activity. Mitazalimab activates antigen-presenting cells, e.g. dendritic cells (DC), to initiate tumor-reactive T cells. Therefore, Mitazalimab induces tumor-specific T cells to infiltrate and kill tumors. Mitazalimab remodels the tumor-infiltrating myeloid microenvironment[1][2]. |
Name | Mitazalimab |
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Description | Mitazalimab (ADC-1013; JNJ-64457107) is FcγR-dependent CD40 agonist with tumor-directed activity. Mitazalimab activates antigen-presenting cells, e.g. dendritic cells (DC), to initiate tumor-reactive T cells. Therefore, Mitazalimab induces tumor-specific T cells to infiltrate and kill tumors. Mitazalimab remodels the tumor-infiltrating myeloid microenvironment[1][2]. |
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Related Catalog | |
Target |
CD40 |
In Vitro | Mitazalimab(1 ng/mL-10 μg/mL)可激活人类前列腺肿瘤或卵巢肿瘤样本中的肿瘤相关巨噬细胞 (TAM)[2]。 |
In Vivo | Mitazalimab(100 μg/小鼠;腹腔注射;单次剂量)激活 naïve hCD40tg 小鼠的脾脏树突细胞和 B 细胞,并在 OVA 再处理条件(200 μg;i.v.;3 次,连续 7 天)下,导致 OVA 特异性 CD8+ T 细胞扩增[1]。 Mitazalimab(100 和 300 μg/小鼠;腹腔注射;接种后第 7、10 和 13 天)诱导携带 MB49(小鼠膀胱肿瘤细胞系)的肿瘤小鼠的血液中促炎细胞因子和趋化因子的释放,并改变肿瘤骨髓细胞组成,减少单核细胞和巨噬细胞,增加粒细胞[1]。 Animal Model: MB49-tumor bearing mice model[1] Dosage: 10, 30, 100 or 300 µg/mouse Administration: Intraperitoneal injection; on day 7, 10 and 13 post-inoculation; sampled at 24 h after final dose Result: Increased the level of IP-10, MIP-1α and TNF-α, but not CXCL1, IFN-γ, IL-6, IL-10, MCP-1 and MIP-2. Resulted in increased frequency of CD44hi CD62L-efector memory CD8+ and CD4+ T cells. |
References |
No Any Chemical & Physical Properties |