Copyright: ©Author(s) 2026.
World J Clin Oncol. May 24, 2026; 17(5): 117391
Published online May 24, 2026. doi: 10.5306/wjco.v17.i5.117391
Published online May 24, 2026. doi: 10.5306/wjco.v17.i5.117391
Table 1 Co-expression of PD-1/C-X-C motif chemokine receptor 3 or PD-L1/C-X-C motif chemokine receptor 3 in T cells and tumor cells. Expression patterns, clinical significance, and evidence strength
| Cell type | Co-express pattern | Significance | Evidence |
| T cells | Programmed death-1/CXCR3, PD-L1/CXCR3 | Strong adverse prognostic markers (associated with advanced disease and short survival). Reflect the exhaustion status and dysfunction of T cells. Dynamic changes can indicate treatment response | Strong; provided specific flow cytometry data, statistical analysis (receiver operating characteristic, survival analysis, multivariate regression), and mechanism discussion |
| Tumor cells | PD-L1/CXCR3 | PD-L1 expression mediates immune escape. Overexpression of CXCR3 may promote tumorigenesis. The two may synergistically promote an immunosuppressive microenvironment | Indirect/inferential; the significance is based on known literature and article background discussion, lacking direct experimental data on co- expression on tumor cells in this article |
- Citation: Chiang ZC, Lin JZ, Chen Q. Immune checkpoint co-expression combined with systemic inflammatory index: A promising approach in prognostic evaluation of lymphoma in Egypt. World J Clin Oncol 2026; 17(5): 117391
- URL: https://www.wjgnet.com/2218-4333/full/v17/i5/117391.htm
- DOI: https://dx.doi.org/10.5306/wjco.v17.i5.117391