ArticleFrontiers in immunology2026
The B7-H3/CD3 immune phenotype identifies prognostic subgroups in neuroblastoma.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- B7-H3-mediated immune regulation in cancer: biological functions and therapeutic opportunities.Frontiers in pharmacology · 2026Review
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19 authors.
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Abstract
Introduction: B7-H3 is an immune checkpoint molecule implicated in tumor immune evasion and adverse prognosis in multiple malignancies. This study aimed to characterize the relationships between tumor-cell B7-H3 expression, immune-cell infiltration, clinicopathological features, and survival in malignant neuroblastic tumors, and to define an immune phenotype with potential translational relevance. Methods: We retrospectively analyzed a population-representative cohort of 81 patients with neuroblastoma or nodular ganglioneuroblastoma diagnosed between 2009 and 2020. B7-H3 expression and CD3 Results: Tumors with high B7-H3 expression demonstrated reduced CD8 Conclusion: The B7-H3 low/CD3 high immune phenotype identifies patients with markedly favorable survival in malignant neuroblastic tumors and retains a protective association after adjustment for established clinical prognostic factors. However, given the limited statistical power of the current cohort, the overall incremental prognostic value of combined B7-H3/CD3 phenotyping requires evaluation in larger, independent cohorts.
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