{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,16]],"date-time":"2026-06-16T05:54:03Z","timestamp":1781589243480,"version":"3.54.5"},"reference-count":31,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,6,16]],"date-time":"2026-06-16T00:00:00Z","timestamp":1781568000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Immunol."],"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>\n                      To investigate the expression of Programmed cell death ligand 1 (PD-L1) in Ameloblastoma (AM) and its correlation with\n                      <jats:italic>\n                        BRAF\n                        <jats:sup>V600E<\/jats:sup>\n                      <\/jats:italic>\n                      mutation as well as the expression of Cytotoxic CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cells (CD8\n                      <jats:sup>+<\/jats:sup>\n                      T) and Forkhead box protein 3 (FoxP3) in the immune microenvironment. And to preliminarily explore the potential association of PD-L1 with the biological behavior and Disease-free survival (DFS) of patients with AM, so as to provide a theoretical reference for clinical diagnosis and treatment.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Fifty formalin-fixed paraffin-embedded (FFPE) specimens of AM were enrolled in this study. Immunohistochemistry (IHC) was performed to detect the expression of\n                      <jats:italic>\n                        BRAF\n                        <jats:sup>V600E<\/jats:sup>\n                      <\/jats:italic>\n                      mutant protein, CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cells, FoxP3\n                      <jats:sup>+<\/jats:sup>\n                      T cells and PD-L1. Molecular testing for the\n                      <jats:italic>\n                        BRAF\n                        <jats:sup>V600E<\/jats:sup>\n                      <\/jats:italic>\n                      mutation was further conducted in 29 eligible AM specimens. PD-L1 expression was evaluated by IHC, and the combined positive score (CPS) \u2265 1 was defined as PD-L1 positivity. The chi-square test and Fisher\u2019s exact test were used for bivariate statistical analysis. Survival analysis was performed using the Kaplan-Meier method with the log-rank test, and the Cox proportional hazards regression model was applied to identify predictive factors for DFS.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of the 50 patients, 42 (84%) were PD-L1 positive. Forty-one cases were\n                      <jats:italic>BRAF<\/jats:italic>\n                      mutation-positive, and 38 of them (92.68%) showed PD-L1 positivity, indicating a significant association between the two (\n                      <jats:italic>p<\/jats:italic>\n                      \u00a0=\u00a00.003). No significant correlations were found between PD-L1 and other major indicators, including CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cells (\n                      <jats:italic>p<\/jats:italic>\n                      \u00a0=\u00a00.247), FoxP3\n                      <jats:sup>+<\/jats:sup>\n                      cells (\n                      <jats:italic>p<\/jats:italic>\n                      \u00a0=\u00a00.702), and pathological subtype (\n                      <jats:italic>p<\/jats:italic>\n                      \u00a0=\u00a00.667). In exploratory survival analysis, patients with high CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cell infiltration exhibited a tendency of prolonged DFS compared with those with low infiltration (HR\u00a0=\u00a00.112, 95%CI: 0.014\u20130.913,\n                      <jats:italic>p<\/jats:italic>\n                      \u00a0=\u00a00.041).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      PD-L1 expression is frequently observed in AM with\n                      <jats:italic>\n                        BRAF\n                        <jats:sup>V600E<\/jats:sup>\n                      <\/jats:italic>\n                      mutation, whereas no significant correlation is identified between PD-L1 and the clinicopathological parameters associated with AM. Within the limitation of relatively short follow-up duration, high CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cell infiltration was indicated to be potentially correlated with favorable DFS in AM patients, which needs further verification in cohorts with longer follow-up.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fimmu.2026.1762600","type":"journal-article","created":{"date-parts":[[2026,6,16]],"date-time":"2026-06-16T05:37:46Z","timestamp":1781588266000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Programmed cell death ligand 1 in correlation with BRAFV600E mutation, molecular characteristics and biological behavior in ameloblastoma"],"prefix":"10.3389","volume":"17","author":[{"given":"Aijing","family":"Pan","sequence":"first","affiliation":[{"name":"Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Bengbu 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