138 Shared frameshift neoantigens are expressed throughout mismatch repair deficient cancer development and are recognized by tissue infiltrating T cells that are dysregulated in advanced lesions
Main Authors: | Matthew Brown, Nina Bhardwaj, Cansu Cimen Bozkus, Aimee L Lucas, Alexandros D Polydorides, Leandra Velazquez, Mesude Bicak, Juhana Habib, Sharonne Holtzman, Mona Saleh, Robert Samstein |
---|---|
Format: | Article |
Language: | English |
Published: |
BMJ Publishing Group
2023-11-01
|
Series: | Journal for ImmunoTherapy of Cancer |
Similar Items
-
Lynch Syndrome and MSI-H Cancers: From Mechanisms to “Off-The-Shelf” Cancer Vaccines
by: Vladimir Roudko, et al.
Published: (2021-09-01) -
Immune escape and resistance to immunotherapy in mismatch repair deficient tumors
by: Guillaume Mestrallet, et al.
Published: (2023-07-01) -
Comparison of personal and shared frameshift neoantigen vaccines in a mouse mammary cancer model
by: Milene Peterson, et al.
Published: (2020-05-01) -
Predicting response and toxicity to immune checkpoint inhibitors in lung cancer using antibodies to frameshift neoantigens
by: Luhui Shen, et al.
Published: (2023-05-01) -
Characterization of shared neoantigens landscape in Mismatch Repair Deficient Endometrial Cancer
by: Elisa De Paolis, et al.
Published: (2024-12-01)