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Fig. 5 | Journal of Translational Medicine

Fig. 5

From: Non-spatial and spatial heterogeneity revealed a suppressive immune feature of Siglec-15 in lung adenocarcinomas

Fig. 5

Siglec-15+ tumor cells or TAMs were strongly associated with the spatial distribution of Tregs and TAMs (n = 189). A Representative composite image, phenotype map, proximity distance map showing CD4+FoxP3+ Tregs within a 20um radius from the nuclear center of each S15 and S15+ tumor cells, (B) or TAMs, (C) and CD68+ TAMs within a 20um radius from the nuclear center of each S15 and S15+ tumor cells. Scale bar, 100 um. D The CD4+FoxP3+ Tregs density around S15+ TAMs was significantly higher than that around S15+ tumor cells. E S15+ tumor cells were closer proximity to CD4+FoxP3+ Tregs compared with S15 tumor cells. F S15+ TAMs were spatially closer to CD4+FoxP3+ Tregs than S15 TAMs, (G) and S15+ tumor cells. J S15+ tumor cells or TAMs were spatially closer to CD4+FoxP3+ Tregs than S15 tumor cells, (K) and spatially closer to CD4+FoxP3+ Tregs than S15 TAMs, regardless of PD-L1 expression. H S15+ tumor cells were surrounded by more CD68+ TAMs, (I) and spatially closer to CD68+ TAMs than S15 tumor cells. L S15+ tumor cells were infiltrated by more CD68+ TAMs than S15 tumor cells, (M) and were spatially closer to CD68+ TAMs than S15 tumor cells, regardless of PD-L1 expression

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