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Cathepsin G Is Expressed by Acute Lymphoblastic Leukemia and Is a Potential Immunotherapeutic Target.

Authors :
Khan M
Carmona S
Sukhumalchandra P
Roszik J
Philips A
Perakis AA
Kerros C
Zhang M
Qiao N
John LSS
Zope M
Goldberg J
Qazilbash M
Jakher H
Clise-Dwyer K
Qiu Y
Mittendorf EA
Molldrem JJ
Kornblau SM
Alatrash G
Source :
Frontiers in immunology [Front Immunol] 2018 Jan 25; Vol. 8, pp. 1975. Date of Electronic Publication: 2018 Jan 25 (Print Publication: 2017).
Publication Year :
2018

Abstract

Cathepsin G (CG) is a myeloid azurophil granule protease that is highly expressed by acute myeloid leukemia (AML) blasts and leukemia stem cells. We previously identified CG1 (FLLPTGAEA), a human leukocyte antigen-A2-restricted nonameric peptide derived from CG, as an immunogenic target in AML. In this report, we aimed to assess the level of CG expression in acute lymphoid leukemia (ALL) and its potential as an immunotherapeutic target in ALL. Using RT-PCR and western blots, we identified CG mRNA and protein, respectively, in B-ALL patient samples and cell lines. We also examined CG expression in a large cohort of 130 patients with ALL via reverse-phase protein array (RPPA). Our data show that CG is widely expressed by ALL and is a poor prognosticator. In addition to endogenous expression, we also provide evidence that CG can be taken up by ALL cells. Finally, we demonstrate that patient ALL can be lysed by CG1-specific cytotoxic T lymphocytes in vitro . Together, these data show high expression of CG by ALL and implicate CG as a target for immunotherapy in ALL.

Details

Language :
English
ISSN :
1664-3224
Volume :
8
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
29422892
Full Text :
https://doi.org/10.3389/fimmu.2017.01975