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Learn how scientists at the University of Pennsylvania are leveraging the strengths of IVT mRNA-LNPs to develop an effective vaccine against Borrelia burgdorferi, the Lyme disease causing bacteria.
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Learn how work presented at ACCR2023 is leveraging IVT mRNA to improve existing cancer immunotherapies or develop new therapy strategies by arming myeloid cells with CARs.
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The potential of cytokines as immunotherapies is limited by their systemic toxicity, therefore, new engineering approaches aim at modifying cytokines for tumor-targeted reconstitution of their activity, providing new opportunities for their use in combina
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Learn how scientists at the Pritzker School of Molecular Engineering, University of Chicago, have engineered a masked Interleukin-12 protein that is preferentially unmasked at tumor sites, thereby reducing adverse events commonly associated with systemic
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Learn how a new platform to regulate CAR T cell activity offers total control, enabling the complete silencing of CAR signaling.
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Learn about a new CRISPR/Cas9 application leveraging its RNA guided specificity to self-assemble peptide fused and inactivated Cas9 onto DNA microarrays.
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Learn how lentiviral vectors promise to offer a safer gene delivery approach for correction of immunological deficits in SCID-ADA.
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Learn how an influenza hemagglutinin nanoparticle vaccine protects against influenza viral strains by inducing broad neutralizing antibodies.
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Learn how structure-guided modifications to CRISPR/Cas12a and Cas9 in the Kleinstiver lab have expanded access to genome sequences by expanding PAM preferences.
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Learn how high throughput DNA assembly helps expedite metabolic engineering for biofuel pathway optimization in microbes.