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Neoantigen screening identifies broad TP53 mutant immunogenicity in patients with epithelial cancers
Parisa Malekzadeh, … , Steven A. Rosenberg, Drew C. Deniger
Parisa Malekzadeh, … , Steven A. Rosenberg, Drew C. Deniger
Published February 4, 2019
Citation Information: J Clin Invest. 2019;129(3):e123791. https://doi.org/10.1172/JCI123791.
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Concise Communication Immunology Oncology

Neoantigen screening identifies broad TP53 mutant immunogenicity in patients with epithelial cancers

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Abstract

Authors

Parisa Malekzadeh, Anna Pasetto, Paul F. Robbins, Maria R. Parkhurst, Biman C. Paria, Li Jia, Jared J. Gartner, Victoria Hill, Zhiya Yu, Nicholas P. Restifo, Abraham Sachs, Eric Tran, Winifred Lo, Robert P.T. Somerville, Steven A. Rosenberg, Drew C. Deniger

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Figure 2

Immunogenic TP53 hot spot mutations could be restricted by common HLA alleles and targeted by TCRs isolated from p53 neoantigen–reactive TILs.

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Immunogenic TP53 hot spot mutations could be restricted by common HLA al...
(A) HLA class I restriction of p53Y220C (patient 5, TIL culture 4259-F1) and p53R248W (patient 9, TIL culture 4266-F1) neoepitopes. Data are mean ± SEM, n = 3 technical replicates. > indicates 1,250 pg/ml IFN-γ. (B) Peptide mapping of CD4+ T cell responses from patient 4 to p53R175H neoepitopes. (C) HLA class II restriction for p53Y220C neoantigen from patient 5. (D) HLA allele frequencies from selected populations (http://www.allelefrequencies.net/default.asp). (E) Specificity of HLA-DRB*13:01/p53R175H–reactive TCR to 25 amino acid p53R175H peptides.

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