Central nervous system (CNS) tumors, particularly gliomas such as glioblastoma (GBM), have the worst prognosis. The median survival time was only 14-16 months. This is largely due to their immunosuppressive tumor microenvironment (TME) and pronounced heterogeneity at the spatial, temporal, cellular and molecular levels (1-3). The intricate crosstalk of cellular and molecular spatiotemporal heterogeneity within these tumors presents significant challenges for developing effective treatment strategies (2-4).Recent advancements, such as the introduction of spatially resolved T cell receptor sequencing (SPTCR-seq) by Benotmyane et al., highlight the rapid evolution of our analytical methods. This technique utilizes optimized target enrichment and long-read sequencing to surpass existing technologies in reconstructing complete TCR architectures and evaluating T cell diversity in cancer. This progress advances our understanding of cancer immunosuppression and signals a broader trend in the field. In addition to spatial analysis, new methodologies are emerging, driving us toward significant clinical benefits. As these technologies continue to evolve, we are optimistic that the coming years will see these innovations translate into noticeable improvements in patient outcomes, indicating that we are moving in the right direction (5).Gene therapy is experiencing a resurgence, highlighted by the recent approval of Todo's oncolytic HSV-1 G47D gene therapy in Japan. This marked a significant milestone in the treatment of residual or recurrent GBM, where Todo et al.'s phase I and II clinical trials have demonstrated promising results, including encouraging one-year survival rates. These trials incorporated histopathological analysis of matched samples taken from primary surgery before treatment and from secondary surgery posttreatment, revealing enhanced recruitment of immune cells in the secondary tissue following gene therapy (6, 7). Furthering this line, Umemura and coauthors employed multiplex spatial analysis in their phase 1 clinical trial to map the distribution of tumor cells, immune cells, and other cellular constituents within the glioma microenvironment. Their findings suggested a significant increase in the immune region characterized by a high density of CD45 + lymphocytes in six out of eight patients following dual viral vector Ad-TK and Ad-Flt3L-based gene therapy (8). Conversely, the tumor region, identified by a high density of SOX2 + tumor cells, showed a decrease in all patients. Interestingly, the analysis revealed that immune cells are often entrapped by myeloid cells in Frontiers in Immunology frontiersin.org 01