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Talacotuzumab

Catalog No. T76883 CAS 1826831-79-1

Synonyms: CSL 362, JNJ 56022473

Talacotuzumab (JNJ 56022473) is an IgG1 fully humanized CD123 neutralizing monoclonal antibody containing a modified Fc structure. Talacotuzumab has a high affinity for CD123, CD32b/c, CD16-158F and CD16-158V, with KD of 0.43 nM, 188 nM, 46 nM and 16.8 nM, respectively. Talacotuzumab inhibits IL-3 signaling in target cells by inhibiting IL-3 binding to CD123. Talacotuzumab induces mutations in the Fc region to increase affinity for CD16 (FCγriiia), thereby enhancing antibody-dependent cell-mediated cytotoxicity (ADCC). Talacotuzumab inhibits leukemia cell growth in xenografted mouse models of acute myeloid leukemia (AML).

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Talacotuzumab

Talacotuzumab, CAS 1826831-79-1

Pack Size	Availability	Price/USD
1 mg	In stock	$ 497.00
5 mg	In stock	$ 1,080.00
10 mg	In stock	$ 1,450.00

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Description	Talacotuzumab (JNJ 56022473) is an IgG1 fully humanized CD123 neutralizing monoclonal antibody containing a modified Fc structure. Talacotuzumab has a high affinity for CD123, CD32b/c, CD16-158F and CD16-158V, with KD of 0.43 nM, 188 nM, 46 nM and 16.8 nM, respectively. Talacotuzumab inhibits IL-3 signaling in target cells by inhibiting IL-3 binding to CD123. Talacotuzumab induces mutations in the Fc region to increase affinity for CD16 (FCγriiia), thereby enhancing antibody-dependent cell-mediated cytotoxicity (ADCC). Talacotuzumab inhibits leukemia cell growth in xenografted mouse models of acute myeloid leukemia (AML).
Targets&IC50	TF-1 cells:33 pM
In vitro	With an IC50 of 5 ng/ml (33 pM), Talacotuzumab (JNJ 56022473; CSL 362) potently mediates antibody-dependent cell-mediated cytotoxicity (ADCC) in TF-1 cells [1]. Following a 24-hour pretreatment at 1 μg/ml,Talacotuzumab inhibits the production of IFN-α in plasmacytoid dendritic cells and eosinophils in SLE (systemic lupus erythematosus) donor and healthy donor plasma-like dendritic cells. This inhibition occurs when these cells are stimulated with TLR7 (imiquimod; 0.5 μM; 6 days) and TLR9 (CpG C; 0.5 μM; 6 days). However, Talacotuzumab does not significantly reduce IFN-α production induced by TLR4 stimulation (LPS; 10 μg/ml). The inhibitory effect of Talacotuzumab on plasmacytoid dendritic cell (pDC) proliferation and expansion induced by TLR7 and TLR9 is achieved through the depletion of pDC [2].
In vivo	In mice with xenografts of acute myeloid leukemia,Talacotuzumab (JNJ 56022473; CSL 362; 300 μg; intraperitoneal injection; three times per week for 5 weeks) significantly delays tumor growth compared to the isotype control [1]. Talacotuzumab (1, 10, 30 mg/kg; subcutaneous injection; single dose) in juvenile cynomolgus monkeys reaches maximum serum concentrations of 12, 190, and 380 μg/ml at doses of 1, 10, and 30 mg/kg, respectively, within 48 hours [2].

Synonyms	CSL 362, JNJ 56022473
Molecular Weight	N/A
CAS No.	1826831-79-1

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store at -80°C

References and Literature

1. S J Busfield, et al. Targeting of acute myeloid leukemia in vitro and in vivo with an anti-CD123 mAb engineered for optimal ADCC. Leukemia. 2014 Nov;28(11):2213-21. 2. Shereen Oon, et al. A cytotoxic anti-IL-3Rα antibody targets key cells and cytokines implicated in systemic lupus erythematosus. JCI Insight. 2016 May 5;1(6):e86131.

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Keywords

Talacotuzumab 1826831-79-1 Immunology/Inflammation Immunology/Inflammation related Interleukin CSL362 CSL-362 JNJ-56022473 JNJ56022473 CSL 362 JNJ 56022473 inhibitor inhibit

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