Spatial immunoprofiling of retroperitoneal leiomyosarcomas reveals intratumoral heterogeneity in immune cell infiltration, checkpoint molecule expression, and tertiary lymphoid structures
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
41081427
PubMed Central
PMC12519586
DOI
10.1080/07853890.2025.2568725
Knihovny.cz E-zdroje
- Klíčová slova
- Leiomyosarcoma, immune cell infiltration, immune checkpoint inhibitors, lymphocyte activation gene 3, tumour heterogeneity,
- MeSH
- antigeny CD274 metabolismus imunologie MeSH
- antigeny CD279 metabolismus imunologie MeSH
- CD antigeny metabolismus MeSH
- ektopické lymfoidní struktury * imunologie patologie MeSH
- indolamin-2,3,-dioxygenasa metabolismus MeSH
- inhibitory kontrolních bodů terapeutické užití MeSH
- leiomyosarkom * imunologie patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové mikroprostředí imunologie MeSH
- protein genu 3 aktivace lymfocytů MeSH
- retroperitoneální nádory * imunologie patologie MeSH
- senioři MeSH
- tumor infiltrující lymfocyty imunologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny CD274 MeSH
- antigeny CD279 MeSH
- CD antigeny MeSH
- CD274 protein, human MeSH Prohlížeč
- IDO1 protein, human MeSH Prohlížeč
- indolamin-2,3,-dioxygenasa MeSH
- inhibitory kontrolních bodů MeSH
- Lag3 protein, human MeSH Prohlížeč
- PDCD1 protein, human MeSH Prohlížeč
- protein genu 3 aktivace lymfocytů MeSH
INTRODUCTION: Leiomyosarcoma (LMS) is a rare, aggressive cancer with limited treatment options at the metastatic stage. The response to immune checkpoint inhibitors (ICIs) is inconsistent, likely due to intratumoral heterogeneity, which is more pronounced in large tumours such as retroperitoneal LMS. METHODS: This study examined heterogeneity in four large treatment-naive LMS tumours (ten samples per tumour) by analysing immune cells, tertiary lymphoid structures (TLSs), checkpoint molecules, and cytokine secretion across different tumour regions. RESULTS: Significant region-dependent differences were observed in immune components, with TLSs present only at tumour margins and inconsistently across samples from the same tumour. Expression levels of programmed cell death 1 (PD-1) and programmed death ligand 1 (PD-L1) varied within individual tumours, and shared immune patterns were identified in specific regions, including elevated indoleamine 2,3-dioxygenase 1, absence of a particular macrophage subpopulation, and reduced PD-1 and lymphocyte activation gene 3 (LAG-3) expression at organ-adjacent margins. Anti-LAG-3 blockade altered cytokine and checkpoint molecule levels in a region-specific manner. CONCLUSION: These findings highlight substantial intratumoral heterogeneity, which may contribute to the variable response to ICI therapy. As immune checkpoint molecule expression influences treatment eligibility, multiple biopsies from different tumour regions may be necessary to assess immune infiltration accurately and guide therapy decisions.
Department of Oncology University Hospital General de Villalba Madrid Spain
Medical Oncology Department Fundacion Jimenez Diaz University Hospital Madrid Spain
Research Health Institute of Fundación Jiménez Díaz Madrid Spain
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