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 to male patients. Furthermore, increased expression of CXCL13 was associated with response to PD-1-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-PD-1 therapy in lung cancer that may need to be considered during patient treatment decisions.
Keyphrases
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- immune response
- poor prognosis
- prognostic factors
- single cell
- peritoneal dialysis
- patient reported outcomes
- young adults
- mass spectrometry
- high resolution
- mesenchymal stem cells
- bone marrow
- case report
- drug delivery
- dendritic cells
- lymph node metastasis
- patient reported
- squamous cell