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<t>Ipilimumab</t> partially restored T cell activation in non-responder patients with NSCLC treated with pembrolizumab plus chemotherapy PBMC from five non-responder patients were stimulated with pembrolizumab ± ipilimumab, in the presence of anti-CD3 and anti-CD28. (A) UMAP graphs for T lymphocyte populations. (B) Two lymphocyte populations differentially present in the two groups of patients were selected and analyzed for the expression of IFN-γ, granzyme B, and IL-10. (C) Frequency of T lymphocyte populations in each stimulus group. Median and interquartile range are shown. Statistical analysis using the Kruskal-Wallis test.
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<t>Ipilimumab</t> partially restored T cell activation in non-responder patients with NSCLC treated with pembrolizumab plus chemotherapy PBMC from five non-responder patients were stimulated with pembrolizumab ± ipilimumab, in the presence of anti-CD3 and anti-CD28. (A) UMAP graphs for T lymphocyte populations. (B) Two lymphocyte populations differentially present in the two groups of patients were selected and analyzed for the expression of IFN-γ, granzyme B, and IL-10. (C) Frequency of T lymphocyte populations in each stimulus group. Median and interquartile range are shown. Statistical analysis using the Kruskal-Wallis test.
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<t>Ipilimumab</t> partially restored T cell activation in non-responder patients with NSCLC treated with pembrolizumab plus chemotherapy PBMC from five non-responder patients were stimulated with pembrolizumab ± ipilimumab, in the presence of anti-CD3 and anti-CD28. (A) UMAP graphs for T lymphocyte populations. (B) Two lymphocyte populations differentially present in the two groups of patients were selected and analyzed for the expression of IFN-γ, granzyme B, and IL-10. (C) Frequency of T lymphocyte populations in each stimulus group. Median and interquartile range are shown. Statistical analysis using the Kruskal-Wallis test.
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Ipilimumab partially restored T cell activation in non-responder patients with NSCLC treated with pembrolizumab plus chemotherapy PBMC from five non-responder patients were stimulated with pembrolizumab ± ipilimumab, in the presence of anti-CD3 and anti-CD28. (A) UMAP graphs for T lymphocyte populations. (B) Two lymphocyte populations differentially present in the two groups of patients were selected and analyzed for the expression of IFN-γ, granzyme B, and IL-10. (C) Frequency of T lymphocyte populations in each stimulus group. Median and interquartile range are shown. Statistical analysis using the Kruskal-Wallis test.

Journal: iScience

Article Title: Circulating cell populations as response predictors and targets to improve immunotherapy in metastatic lung cancer

doi: 10.1016/j.isci.2026.116124

Figure Lengend Snippet: Ipilimumab partially restored T cell activation in non-responder patients with NSCLC treated with pembrolizumab plus chemotherapy PBMC from five non-responder patients were stimulated with pembrolizumab ± ipilimumab, in the presence of anti-CD3 and anti-CD28. (A) UMAP graphs for T lymphocyte populations. (B) Two lymphocyte populations differentially present in the two groups of patients were selected and analyzed for the expression of IFN-γ, granzyme B, and IL-10. (C) Frequency of T lymphocyte populations in each stimulus group. Median and interquartile range are shown. Statistical analysis using the Kruskal-Wallis test.

Article Snippet: Ipilimumab, Yervoy , Bristol-Myers Squibb , N/A.

Techniques: Activation Assay, Expressing