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Lipid Nanoparticle Delivery System for mRNA Encoding B7H3 . . . - PubMed The therapeutic use of bispecific T-cell engaging (BiTE) antibodies has shown great potential for treating malignancies BiTE can simultaneously engage CD3ε on T cells and tumor antigen on cancer cells, thus exerting an effective antitumor effect
Recent Advances in Site-Specific Lipid Nanoparticles for mRNA Delivery In another study, Huang et al use a novel LNP to deliver mRNA encoded with bispecific T-cell engaging (BiTE) antibody B7H3-CD3, which could bind with B7H3 receptors on tumor cells and CD3 receptors on T cells simultaneously, thereby inducing the recognition of tumor cells by T cells and antitumor efficacy 63 The LNP was composed of DMG-PEG
Lipid Nanoparticle Delivery System for mRNA Encoding B7H3â redirected . . . Here, we show that a novel and liver-targeted ionizable lipid nanoparticle delivery system for mRNA encoding B7H3×CD3 BiTE exerts potent antitumor activity against hematologic and solid tumors compared with purified recombinant BiTE
1358 Tissue-targeted lipid nanoparticle delivery for mRNA encoding . . . However, the relatively short serum half-life of recombinant BiTE, and reported CRS and neurotoxicity have limited its applications Here, we describe tissue targeted LNP-mRNA encoding BiTE that expressed long-lasting and therapeutic levels of BiTE protein at the tar-geted tumor sites
GitHub - cosbi-research PBPKmRNABiTE: A multi-scale physiologically . . . SCM_simulation m: Source code for the model simulation for both recombinant and mRNA-encoded protein administration in the Short Chain Model Fixing the dose injected and the observation time window allows computing the time evolution of BiTEs' concentration in blood