Entity: University of Texas MD Anderson Cancer Center
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University of Texas MD Anderson Cancer Center

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The 2025 study reported that among patients with immunologically "cold" tumors, adding an mRNA COVID-19 vaccine within about 100 days of starting immune checkpoint inhibitor therapy was associated with a nearly five-fold increase in three-year overall survival.
October 19, 2025 high temporal
Subset analysis within the same observational clinical dataset focused on tumors characterized as immunologically cold (typically resistant to immunotherapy).
The 2025 study found that seasonal non-mRNA vaccines for influenza and pneumonia did not show the same tumor responsiveness or survival-associated effects as the mRNA COVID-19 vaccine when administered near the start of immune checkpoint inhibitor therapy.
October 19, 2025 high temporal
Comparative observation within the clinical dataset contrasting mRNA COVID-19 vaccine effects with non-mRNA influenza and pneumococcal vaccines.
A 2025 study by researchers at the University of Osaka reported a protocol combining signaling molecules and other compounds that increases Foxp3 expression in induced regulatory T cells (iTregs), induces epigenetic modifications associated with Treg identity, and produced iTregs that maintained Foxp3 expression and provided immune-suppressive effects in mouse models for at least six weeks.
October 06, 2025 high study
Core experimental findings on a method to stabilize iTregs reported in 2025