Novel Platform Design for Screening of Optimal Immune Receptors for Antibody Circuits
NUNEZ-BAEZ-MASTEROFMEDICALSCIENCESTHESIS-2019.pdf (6.695Mb)(embargoed until: 2021-05-01)
Núñez-Báez, Sergio Gabriel
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CitationNúñez-Báez, Sergio Gabriel. 2019. Novel Platform Design for Screening of Optimal Immune Receptors for Antibody Circuits. Master's thesis, Harvard Medical School.
AbstractIn recent years, cancer immunotherapy has acquired a central role in the combat of cancer, an example being the use of T-cell engaging bispecific antibodies which offer a relatively simple approach to engaging patients’ T cells to target cancer cells in an HLA-independent manner. Unfortunately, trials of bispecific T-cell engaging antibodies (BiTE) have shown either severe adverse events or death that remains a major barrier to broad implementation. T cell engaging antibody circuits (TEACs) is a novel immune cell engaging platform that allows for exquisite targeting of cancer cells with minimal targeting of healthy cells. Beyond T-cells, our interest is to use this platform to engage the innate compartment. For the effective design of TEAC molecules that can redirect innate immune responses, we developed a platform that allows for dynamic screening of potential immunoreceptor targets called adaptor bispecific antibody circuits (ABA-C). It accomplishes this by using an adaptor bispecific antibody (ABA) to differentially recognize and bridge antibodies against target antigens on a cancer cell and a target immunoreceptor, emulating the synapse created by TEACs. As a model to investigate the potential of ABA-C in activating immune cells, we chose prostate adenocarcinoma as studies have linked innate immunity with its progression. Data shows that ABA-C can activate T-cells in vitro at comparable levels with TEACs in a highly specific manner at micromolar concentrations of target antigen antibody, independent of target antigen identity or cell line used. Further studies will look to use ABA-C to screen optimal activating immunoreceptors on macrophages, as their inflammatory subsets have been associated to better prognoses on prostate cancer patients.
Citable link to this pagehttp://nrs.harvard.edu/urn-3:HUL.InstRepos:42057397