Human parainfluenza virus serotypes differ in their kinetics of replication and cytokine secretion in human tracheobronchial airway epithelium
Cytokines;Chemokines;细胞因子;趋化因子;MSD;Cytokines;Chemokines- Virology.
- 2012
- 3.513
- 4(16):2013-26.
- Human,Mouse,Non-Human Primate,Rat
- MSD
- Cell culture supernatants
- 呼吸系统
- 其它细胞
- 流感
- I-TAC, IL-6, IL-8, IP-10, MCP-1, RANTES
相关货号
LXMH04-4LXMH07-4LXMH09-1LXMH09-2LXMH10-9LXMH111-1LXMH44-1LXMH46-1LXMH54-1LXMH87-1LXMM06-5LXMM08-1LXMM08-2LXMM09-1LXMM10-3LXMM50-1LXMM58-1LXMN03-1LXMN05-1LXMN06-3
Abstract
Background: The standard safety evaluation of biotherapeutics includes assessment of immunogenicity. Anti-therapeutic antibodies (ATA) can be detected in serum using immunoassays with a bridging format. However, these assays can be subject to interference.
Results: In the bridging ATA assay for 3A5 TDC, an antibody-drug conjugate that binds to the multimeric extracellular domain of MUC16 (CA125), soluble CA125 in the serum caused false-positive results by binding to the ATA assay reagents. This interaction was blocked by wheat germ agglutinin lectin as it binds to the glycans in CA125; thus, the specificity of the assay improved.
Conclusion: The assay development and validation results showed that the addition of wheat germ agglutinin eliminates the interference from circulating CA125 without impacting the ability to detect ATA.
Results: In the bridging ATA assay for 3A5 TDC, an antibody-drug conjugate that binds to the multimeric extracellular domain of MUC16 (CA125), soluble CA125 in the serum caused false-positive results by binding to the ATA assay reagents. This interaction was blocked by wheat germ agglutinin lectin as it binds to the glycans in CA125; thus, the specificity of the assay improved.
Conclusion: The assay development and validation results showed that the addition of wheat germ agglutinin eliminates the interference from circulating CA125 without impacting the ability to detect ATA.
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