Publications by authors named "Mauro Poggio"

Article Synopsis
  • Immune checkpoint inhibition (ICI) has changed cancer therapy, but only some patients experience long-term benefits, highlighting the need for new targets and treatments.* -
  • Researchers utilized the 23andMe database to find a genetic signature linking variations that affect both cancer and immune disease risks, discovering key genes like CD200 and CD200R1.* -
  • They developed a high-affinity antibody (23ME-00610) that inhibits the CD200:CD200R1 interaction, which enhances T-cell activity and reduces tumor growth in mouse models of melanoma.*
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PD-L1 on the surface of tumor cells binds its receptor PD-1 on effector T cells, thereby suppressing their activity. Antibody blockade of PD-L1 can activate an anti-tumor immune response leading to durable remissions in a subset of cancer patients. Here, we describe an alternative mechanism of PD-L1 activity involving its secretion in tumor-derived exosomes.

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Cancer cells develop mechanisms to escape immunosurveillance, among which modulating the expression of immune suppressive messenger RNAs is most well-documented. However, how this is molecularly achieved remains largely unresolved. Here, we develop an in vivo mouse model of liver cancer to study oncogene cooperation in immunosurveillance.

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We apply the time-frequency analysis to the endocavitarian signal of patients suffering from paroxysmal atrial fibrillation. The time-frequency spectrum reveals the components of the endocavitarian signal. These components are located in the regions of the time-frequency domain that differ for in-rhythm and in-atrial fibrillation signals.

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