ICOS is presented as a costimulatory receptor used here to characterize tumor-infiltrating lymphocytes in LUAD. The study evaluates ICOS-positive TIL density and subset-specific ICOS expression.
First-pass extracted concept
ICOS
Aliases
Inducible T cell costimulator
Extracted Explainers
What the tool is doing
Resources required
What problem it solves
What it does not solve
Evidence Snippets
Supporting Sources
Linked Claims
ICOS-positive tumor-infiltrating lymphocyte density was significantly higher in HLA-DR-strong tumors.
ICOS+ TIL density was significantly higher in HLA-DR-strong tumors
Because CD4-positive non-Tregs were numerically predominant, ICOS-positive CD4-positive non-Tregs constituted the largest ICOS-positive fraction in lung adenocarcinoma.
Because CD4+ non-Tregs were numerically predominant, ICOS+CD4+ non-Tregs constituted the largest ICOS+ fraction.
Among HLA-DR-strong tumors, ICOS-high patients tended toward longer cancer-specific survival.
among HLA-DR-strong tumors, ICOS-high patients tended toward longer cancer-specific survival
In resected lung adenocarcinoma, ICOS-positive tumor-infiltrating lymphocyte density correlated with each measured T-cell subset density.
ICOS+ TIL density correlated with each T cell subset.
Multiplex analysis showed that ICOS positivity was highest among Tregs, followed by CD4-positive non-Tregs and then CD8-positive tumor-infiltrating lymphocytes.
Multiplex analysis showed the highest ICOS positivity among Tregs, followed by CD4+ non-Tregs and CD8+ TILs.
ICOS had no overall prognostic impact in the full lung adenocarcinoma cohort.
ICOS had no overall prognostic impact
Single-cell RNA-seq analysis corroborated the subset-specific ICOS expression findings from multiplex immunohistochemistry.
Single-cell RNA-seq analysis corroborated these findings.