Tralokinumab
- Product Name
- Tralokinumab
- CAS No.
- 1044515-88-9
- Chemical Name
- Tralokinumab
- Synonyms
- Tralokinumab;CAT-354|||LP 0162;Tralokinumab (anti-IL-13);Research Grade Tralokinumab;Research Grade Tralokinumab(DHE07703)
- CBNumber
- CB68080758
- Formula Weight
- 0
- MOL File
- Mol file
Tralokinumab Property
- storage temp.
- Store at -20°C
- form
- Liquid
- color
- Colorless to light yellow
Tralokinumab Chemical Properties,Usage,Production
Uses
Tralokinumab (CAT354) is a humanized IgG4 monoclonal antibody that specifically binds to and neutralizes IL-13. Tralokinumab can be used in the research of diseases such as asthma, atopic dermatitis, and pulmonary fibrosis[1][2].
in vivo
Tralokinumab (3 mg/kg; intraperitoneal injection; once every other day; from day 35 to day 63) can inhibit pulmonary fibrosis and reduce epithelial cell apoptosis in a humanized SCID mouse model of pulmonary fibrosis[2].
| Animal Model: | Female C.B-17-scid-beige (C.B-17SCID/bg) mice received single-cell preparations of IPF and normal fibroblasts via tail vein injection[2] |
| Dosage: | 3 mg/kg |
| Administration: | Intraperitoneal injection; once every other day; from day 35 to day 63 |
| Result: | Blocked aberrant lung remodeling, promoted lung repair and restored epithelial integrity. Significantly decreased fibrotic alterations. Reduced serum CC16 (a marker of epithelial injury) and reduced BAL caspase 3 activity. Enhanced the expression of epithelial-associated genes, including E-cadherin and all of the surfactants. |
IC 50
IL-13
References
[1] A Wollenberg, et al. Tralokinumab for moderate-to-severe atopic dermatitis: results from two 52-week, randomized, double-blind, multicentre, placebo-controlled phase III trials (ECZTRA 1 and ECZTRA 2). Br J Dermatol. 2021 Mar;184(3):437-449. DOI:10.1111/bjd.19574
[2] Murray LA, et al. Targeting interleukin-13 with tralokinumab attenuates lung fibrosis and epithelial damage in a humanized SCID idiopathic pulmonary fibrosis model. Am J Respir Cell Mol Biol. 2014 May;50(5):985-94. DOI:10.1165/rcmb.2013-0342OC
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