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Qualitative analysis of tumor-infiltrating lymphocytes across human tumor types reveals a higher proportion of bystander CD8+ T cells in non-melanoma cancers compared to melanoma
- Source :
- Gokuldass , A , Draghi , A , Papp , K , Borch , T H , Nielsen , M , Westergaard , M C W , Andersen , R , Schina , A , Bol , K F , Chamberlain , C A , Presti , M , Met , Ö , Harbst , K , Lauss , M , Soraggi , S , Csabai , I , Szállási , Z , Jönsson , G , Svane , I M & Donia , M 2020 , ' Qualitative analysis of tumor-infiltrating lymphocytes across human tumor types reveals a higher proportion of bystander CD8 + T cells in non-melanoma cancers compared to melanoma ' , Cancers , vol. 12 , no. 11 , 3344 , pp. 1-15 .
- Publication Year :
- 2020
-
Abstract
- Background: Human intratumoral T cell infiltrates can be defined by quantitative or qualitative features, such as their ability to recognize autologous tumor antigens. In this study, we reproduced the tumor-T cell interactions of individual patients to determine and compared the qualitative characteristics of intratumoral T cell infiltrates across multiple tumor types. Methods: We employed 187 pairs of unselected tumor-infiltrating lymphocytes (TILs) and autologous tumor cells from patients with melanoma, renal-, ovarian-cancer or sarcoma, and single-cell RNA sequencing data from a pooled cohort of 93 patients with melanoma or epithelial cancers. Measures of TIL quality including the proportion of tumor-reactive CD8+ and CD4+ TILs, and TIL response polyfunctionality were determined. Results: Tumor-specific CD8+ and CD4+ TIL responses were detected in over half of the patients in vitro, and greater CD8+ TIL responses were observed in melanoma, regardless of previous anti-PD-1 treatment, compared to renal cancer, ovarian cancer and sarcoma. The proportion of tumor-reactive CD4+ TILs was on average lower and the differences less pronounced across tumor types. Overall, the proportion of tumor-reactive TILs in vitro was remarkably low, implying a high fraction of TILs to be bystanders, and highly variable within the same tumor type. In situ analyses, based on eight single-cell RNA-sequencing datasets encompassing melanoma and five epithelial cancers types, corroborated the results obtained in vitro. Strikingly, no strong correlation between the proportion of CD8+ and CD4+ tumor-reactive TILs was detected, suggesting the accumulation of these responses in the tumor microenvironment to follow non-overlapping biological pathways. Additionally, no strong correlation between TIL responses and tumor mutational burden (TMB) in melanoma was observed, indicating that TMB was not a major dri
Details
- Database :
- OAIster
- Journal :
- Gokuldass , A , Draghi , A , Papp , K , Borch , T H , Nielsen , M , Westergaard , M C W , Andersen , R , Schina , A , Bol , K F , Chamberlain , C A , Presti , M , Met , Ö , Harbst , K , Lauss , M , Soraggi , S , Csabai , I , Szállási , Z , Jönsson , G , Svane , I M & Donia , M 2020 , ' Qualitative analysis of tumor-infiltrating lymphocytes across human tumor types reveals a higher proportion of bystander CD8 + T cells in non-melanoma cancers compared to melanoma ' , Cancers , vol. 12 , no. 11 , 3344 , pp. 1-15 .
- Notes :
- application/pdf, English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1250229501
- Document Type :
- Electronic Resource