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Rapid Autopsy to Define Dendritic Cell Spatial Distribution and T Cell Association in Lung Adenocarcinoma. | LitMetric

AI Article Synopsis

  • - The presence and distribution of conventional dendritic cells (cDCs) in the tumor microenvironment (TME) are linked to immunotherapy responses, with cDC1 activating CD8+ T cells and cDC2 regulating CD4+ T cells. - A study of lung adenocarcinoma patients revealed that cDC1 and cDC2 primarily resided in the stroma, while mature regulatory cDCs were more concentrated in actual tumors, indicating their functional roles depend on their location. - The research showed that lung and lymph node tumors had higher levels of T cells and cDCs compared to liver tumors, and while early and late-stage disease had similar T cell and cDC1 proportions, late-stage disease had higher levels of

Article Abstract

Immunotherapy response is associated with the presence of conventional dendritic cells (cDCs). cDC type 1 (cDC1) is critically important for CD8+ T cell activation, cDC type 2 (cDC2) regulates CD4+ T cell responses, and mature regulatory cDCs may dampen T cell responses in the tumor microenvironment (TME). However, we lack a clear understanding of cDC distribution in the human TME, cDC prevalence in metastatic sites, and cDC differences in early- versus late-stage disease. Rapid autopsy specimens of 10 patients with lung adenocarcinoma were evaluated to detect cDCs and immune cells via multiplex immunofluorescence using 18 markers and 42 tumors. First, we found that T cells, cDC1, and cDC2 were confined to stroma, whereas mature regulatory DCs were enriched in tumor, suggesting unique localization-specific functions. Second, lung and lymph node tumors were more enriched in T cells and cDCs than liver tumors, underscoring differences in the TME of metastatic sites. Third, although the proportion of T cells and cDC1 did not differ in different stages, an increase in the proportion of cDC2 and macrophages in late stage suggests potential differences in regulation of T cell responses in different stages. Collectively, these findings provide new, to our knowledge, insights into cDC biology in human cancer that may have important therapeutic implications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11404669PMC
http://dx.doi.org/10.4049/jimmunol.2400234DOI Listing

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