z-logo
open-access-imgOpen Access
Multiple antibodies targeting tumor-specific mutations redirect immune cells to inhibit tumor growth and increase survival in experimental animal models
Author(s) -
G. S. Shukla,
Stephanie C. Pero,
Yini Sun,
Langhua Mei,
F. Zhang,
Giselle L. Saulnier Sholler,
David N. Krag
Publication year - 2019
Publication title -
clinical and translational oncology
Language(s) - English
Resource type - Journals
eISSN - 1699-3055
pISSN - 1699-048X
DOI - 10.1007/s12094-019-02235-3
Subject(s) - antibody , effector , antigen , medicine , immune system , population , melanoma , cancer research , polyclonal antibodies , ex vivo , immunology , in vivo , biology , microbiology and biotechnology , environmental health
T cell therapy for cancer involves genetic introduction of a target-binding feature into autologous T cells, ex vivo expansion and single large bolus administration back to the patient. These reprogrammed T cells can be highly effective in killing cells, but tumor heterogeneity results in regrowth of cells that do not sufficiently express the single antigen being targeted. We describe a cell-based therapy that simultaneously targets multiple tumor-specific antigens.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom