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. Author manuscript; available in PMC: 2022 Dec 1.
Published in final edited form as: Nat Biomed Eng. 2021 Jul 19;5(12):1426–1436. doi: 10.1038/s41551-021-00766-1

Fig. 1 ∣. Immune evasion by human cancer cells within metastatic LNs.

Fig. 1 ∣

a, Representative IF staining of metastatic LNs from patients with head and neck, colon and breast cancer. Scale bar, 1.2 mm. The number of images taken is reflected in the n values for b–d. The dashed lines indicate the margin of the LN lesion. b–d, Lymphocyte quantification within the non-tumour area (NT) and tumour area (T) of metastatic LNs from patients with head and neck cancer (b), colon cancer (c) and breast cancer (d). n = 9 patients with head and neck cancer (n = 8 (non-tumour B-cell area), n = 9 (non-tumour T-cell area) and n = 9 (tumour B- and T-cell area)). T- and B-cell area fraction from n = 13 patients with colon cancer was measured (n = 18 (non-tumour B-cell area), n = 19 (non-tumour T-cell area) and n = 21 (tumour B- and T-cell area)). T- and B-cell area fraction from n = 7 patients with breast cancer was measured (n = 12 (non-tumour B- and T-cell area) and n = 15 (tumour B- and T-cell area)). e, Representative IF staining of CD68+ macrophages (red) in a non-metastatic TDLN and a metastatic LN from a patient with head and neck cancer. Cancer cells are stained green (cytokeratin+), and DAPI (blue) stains all nucleated cells. n = 5 images taken from n = 5 non-metastatic LNs, n = 5 images from n = 5 metastatic LNs. Scale bar, 500 μm. f, Quantification of CD68+ macrophages within LN tumour and non-tumour areas from patients with head and neck squamous cell carcinoma (HNSCC). n = 5 LNs from n = 5 different patients; two of the LNs did not have a non-tumour area. Data are mean ± s.e.m. For b–d and f, significance was tested using two-tailed paired Student’s t-tests (b–d) and an unpaired Student’s t-test (f).