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p95HER2-T cell bispecific antibody for breast cancer treatment.

Authors :
Rius Ruiz I
Vicario R
Morancho B
Morales CB
Arenas EJ
Herter S
Freimoser-Grundschober A
Somandin J
Sam J
Ast O
Barriocanal ÁM
Luque A
Escorihuela M
Varela I
Cuartas I
Nuciforo P
Fasani R
Peg V
Rubio I
Cortés J
Serra V
Escriva-de-Romani S
Sperinde J
Chenna A
Huang W
Winslow J
Albanell J
Seoane J
Scaltriti M
Baselga J
Tabernero J
Umana P
Bacac M
Saura C
Klein C
Arribas J
Source :
Science translational medicine [Sci Transl Med] 2018 Oct 03; Vol. 10 (461).
Publication Year :
2018

Abstract

T cell bispecific antibodies (TCBs) are engineered molecules that include, within a single entity, binding sites to the T cell receptor and to tumor-associated or tumor-specific antigens. The receptor tyrosine kinase HER2 is a tumor-associated antigen in ~25% of breast cancers. TCBs targeting HER2 may result in severe toxicities, likely due to the expression of HER2 in normal epithelia. About 40% of HER2-positive tumors express p95HER2, a carboxyl-terminal fragment of HER2. Using specific antibodies, here, we show that p95HER2 is not expressed in normal tissues. We describe the development of p95HER2-TCB and show that it has a potent antitumor effect on p95HER2-expressing breast primary cancers and brain lesions. In contrast with a TCB targeting HER2, p95HER2-TCB has no effect on nontransformed cells that do not overexpress HER2. These data pave the way for the safe treatment of a subgroup of HER2-positive tumors by targeting a tumor-specific antigen.<br /> (Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)

Details

Language :
English
ISSN :
1946-6242
Volume :
10
Issue :
461
Database :
MEDLINE
Journal :
Science translational medicine
Publication Type :
Academic Journal
Accession number :
30282693
Full Text :
https://doi.org/10.1126/scitranslmed.aat1445