{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T02:55:52Z","timestamp":1777949752509,"version":"3.51.4"},"reference-count":34,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T00:00:00Z","timestamp":1777852800000},"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. Oncol."],"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Adjuvant immune checkpoint inhibitors (ICI) have improved survival in stage III cutaneous melanoma, yet many patients do not benefit. The tumor microenvironment is pivotal for durable responses; defining cellular composition can pinpoint immune components promoting anti-tumor activity and identify biomarkers associated with improved outcomes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Method<\/jats:title>\n                    <jats:p>Regional lymph nodes (RLNs) were obtained at surgery from 29 patients with stage III melanoma. Eligible patients received adjuvant anti-PD-1 (\u03b1PD-1; pembrolizumab or nivolumab). Mass cytometry (CyTOF) was used to determine cellular composition of pre-treatment surgical specimens. NanoString bulk gene expression data from 125 patients receiving surgery without adjuvant therapy were used to evaluate trends observed in the CyTOF dataset.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Higher proportions of CD103\n                      <jats:sup>+<\/jats:sup>\n                      PD-1\n                      <jats:sup>+<\/jats:sup>\n                      CD8\n                      <jats:sup>+<\/jats:sup>\n                      (T\n                      <jats:sub>RM<\/jats:sub>\n                      ) T cells and plasmablast-like CD38\n                      <jats:sup>hi<\/jats:sup>\n                      CD19\n                      <jats:sup>dim<\/jats:sup>\n                      cells were associated with improved prognosis in the CyTOF cohort. In the untreated cohort, a\n                      <jats:italic>\u201cB cell excluded\u201d<\/jats:italic>\n                      subgroup (&amp;lt; 2.5% tumor-infiltrating lymphocyte pathology score) had worse outcome, showing reduced B cell score and lower expression of activation genes including\n                      <jats:italic>CD38<\/jats:italic>\n                      , without change in CD8\n                      <jats:sup>+<\/jats:sup>\n                      T cell score.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Baseline infiltration of CD8\n                      <jats:sup>+<\/jats:sup>\n                      T\n                      <jats:sub>RM<\/jats:sub>\n                      and plasmablast-like CD38\n                      <jats:sup>hi<\/jats:sup>\n                      CD19\n                      <jats:sup>dim<\/jats:sup>\n                      cells in RLN is strongly associated with prolonged distant metastasis-free survival in patients receiving \u03b1PD-1, supporting their potential as prognostic biomarkers in stage III melanoma.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fonc.2026.1815008","type":"journal-article","created":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T04:24:58Z","timestamp":1777868698000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["CD38hiCD19dim cells in lymph nodes predict favorable prognosis in patients with stage III melanoma receiving adjuvant PD-1-blockade"],"prefix":"10.3389","volume":"16","author":[{"given":"Ieva","family":"Ailte","sequence":"first","affiliation":[{"name":"Department of Tumor Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital","place":["Oslo, 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