T-Cell Expression of CXCL13 is Associated with Immunotherapy Response in a Sex-Dependent Manner in Patients with Lung Cancer.
Michelle PhersonDavid DeBruinChinye NwokoloKatey S HuntAlexander PieningMaureen J DonlinStephen T FerrisRyan M TeagueRichard J DiPaoloElise AlspachPublished in: Cancer immunology research (2024)
Emerging evidence in preclinical models demonstrates that antitumor immunity is not equivalent between males and females. However, more investigation in patients and across a wider range of cancer types is needed to fully understand sex as a variable in tumor immune responses. We investigated differences in T-cell responses between male and female patients with lung cancer by performing sex-based analysis of single cell transcriptomic datasets. We found that the transcript encoding CXC motif chemokine ligand 13 (CXCL13), which has recently been shown to correlate with T-cell tumor specificity, is expressed at greater levels in T cells isolated from female compared with male patients. Furthermore, increased CXCL13 expression was associated with response to PD1-targeting immunotherapy in female but not male patients. These findings suggest that there are sex-based differences in T-cell function required for response to anti-PD1 therapy in lung cancer that may need to be considered during patient treatment decisions. See related Spotlight by Cruz-Hinojoza and Stromnes, p. 952.
Keyphrases
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- single cell
- immune response
- prognostic factors
- peritoneal dialysis
- drug delivery
- patient reported outcomes
- cell therapy
- cancer therapy
- papillary thyroid
- mesenchymal stem cells
- inflammatory response
- bone marrow
- high resolution
- single molecule
- high speed
- smoking cessation
- drug induced