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Written and prepared by:
Remziye E. Wessel, Nardin Ageeb, Joseph M. Obeid, Ileana Mauldin, Kate A. Goundry, Gabriel F. Hanson, Mahdin Hossain, Chad Lehman, Ryan D. Gentzler, Nolan A. Wages, Craig L. Slingluff Jr, Timothy N.J. Bullock, Sepideh Dolatshahi, Michael G. Brown
Explore how spatial colocalization of natural killer (NK) and CD8 T cells impacts survival in non-small cell lung cancer (NSCLC) despite MHC class I loss. This study reveals that high densities of NK and CD8 T cells, particularly when colocalized, correlate with improved disease-free and overall survival. The findings suggest potential for combined immunotherapies targeting both NK and CD8 T cells to enhance anti-tumor immunity, even in tumors with MHC-I loss.
Study shows spatial colocalization of NK and CD8 T cells enhances survival despite MHC-I loss in NSCLC.
Research uses multiplex immunofluorescence to analyze immune cell infiltration and MHC-I expression in NSCLC.
NK cells colocalize with CD8 T cells in MHC-I+ NSCLC tumors, improving patient outcomes.
Study reveals MHC-I loss in NSCLC tumors affects NK and CD8 T cell infiltration and activity.
IFNγ+ NK and CD8 T cells cluster in MHC-I+ regions, suggesting coordinated tumor control in NSCLC.
Findings support combined NK and T cell therapies to enhance antitumor immunity in NSCLC with MHC-I loss.
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