Extended Data Fig. 2: Development of in vivo lentiviral and organoid models of CRC with neoantigen expression. | Nature Cancer

Extended Data Fig. 2: Development of in vivo lentiviral and organoid models of CRC with neoantigen expression.

From: Low neoantigen expression and poor T-cell priming underlie early immune escape in colorectal cancer

Extended Data Fig. 2: Development of in vivo lentiviral and organoid models of CRC with neoantigen expression.The alternative text for this image may have been generated using AI.

(a) Lentiviruses used to initiate colon tumors in Apcflox/flox and Apcflox/flox; Rag2-/- mice. (b) Efficiency of tumor formation 16 weeks post-injection. N = independent animals. Significance assessed by two-tailed Wilcoxon Rank Sum with Holm’s correction for multiple comparisons. (c) Antigen expression in LucOS-induced tumors in Rag2-/- (left) and wild-type (right) mice at 12 weeks (colonoscopy above, bioluminescence below). (d) Efficiency of tumor induction with LucOS lentivirus at 20,000 and 100,000 transduction units (TU)/μl. N = 26 independent animals. (e) Antigen expression (bioluminescence). N = 26 independent animals. Significance assessed by two-tailed Wilcoxon Rank Sum. (f) Antigen expression in LucOS-induced tumors with continuous T-cell depletion at 5 weeks (left) and 7 weeks after T-cell depletion (right), and colonoscopy (above). (g) Antigen expression versus relative tumor size (percent of colon occluded) following withdrawal of depleting antibodies. N = 4 independent animals. (h) Correlation of antigen expression and tumor burden in Rag2-/- (dark pink) and αCD4/8 (light pink)-treated mice 12 weeks post-injection with LucOS. N = 17 independent animals. Significance measured by Spearman’s rank-order correlation. (i) noSIIN, hiSIIN, and loSIIN organoids grown in the absence of WNT. Scale bars = 1 mm. Representative of N = 3 independent cultures. (j) Top 10 mutated genes in MSK-IMPACT colon adenocarcinoma (cBioPortal). (k) Lentiviral constructs used to generate organoids expressing only EGFP (noSIIN-GFP) and SIINFEKL expression variants. (l) Linear regression with Pearson correlation of SIINFEKL abundance (TMT-MS) versus mScarletSIIN MFI (flow cytometry). TMT-MS was performed on three independent preparations of each line. (m) H&E and IHC of noSIIN primary colon tumor 42 days post-transplant. Representative of N = 9 independent animals. Scale bar = 100 μM. (n-o) Images of dimSIIN (n) and midSIIN (o) tumors that formed in N = 2/9 and 1/9 transplanted animals, respectively. (p) Lentiviral constructs used to generate organoids expressing SIYRYYGL, ITYTWTRL, and VGFNFRTL at high and low levels. (q) ITYTWTRL and VGFNFRTL tetramer-specific CD8+ T cells infiltrating 42-day loITY and loVGF tumors by flow cytometry. Representative of N = 10 loITY and 9 loVGF transplanted animals.

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