Publications by authors named "A van Elsas"

The greatest challenge in cancer therapy is to eradicate cancer cells with minimal damage to normal cells. Targeted therapy has been developed to meet that challenge, showing a substantially increased therapeutic index compared with conventional cancer therapies. Antibodies are important members of the family of targeted therapeutic agents because of their extraordinarily high specificity to the target antigens.

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Monoclonal antibodies have become an important class of therapeutics in the last 30 years. Because the mechanism of action of therapeutic antibodies is intimately linked to their binding epitopes, identification of the epitope of an antibody to the antigen plays a central role during antibody drug development. The gold standard of epitope mapping, X-ray crystallography, requires a high degree of proficiency with no guarantee of success.

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IL-12 is a potent cytokine for cancer immunotherapy. However, its systemic delivery as a recombinant protein has shown unacceptable toxicity in the clinic. Currently, the intratumoral injection of IL-12-encoding mRNA or DNA to avoid such side effects is being evaluated in clinical trials.

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Single-cell technologies are currently widely applied to obtain a deeper understanding of the phenotype of single-cells in heterogenous mixtures. However, integrated multilayer approaches including simultaneous detection of mRNA, protein expression, and intracellular phospho-proteins are still challenging. Here, we combined an adapted method to in vitro-differentiate peripheral B-cells into antibody-secreting cells (ASCs) (i.

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Article Synopsis
  • T cell engager (TCE) antibodies are innovative cancer treatments that connect T-cells to tumor cells by binding to both T-cell receptors (CD3E) and tumor markers (TAA).
  • The study focuses on a bispecific antibody format (IgG-like Fab x sdAb-Fc) that targets mEGFR on tumors and mCD3E on T-cells, analyzing the effect of hinge design in the sdAb.
  • The findings reveal that a shorter hinge (23 amino acids) enhances tumor cell elimination and T-cell activation compared to a longer hinge (39 amino acids), suggesting that small design modifications can significantly boost the effectiveness of these therapeutic antibodies.
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