Mesothelin, a novel immunotherapy target for triple negative breast cancer

被引:0
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作者
Julia Tchou
Liang-Chuan Wang
Ben Selven
Hongtao Zhang
Jose Conejo-Garcia
Hossein Borghaei
Michael Kalos
Robert H. Vondeheide
Steven M. Albelda
Carl H. June
Paul J. Zhang
机构
[1] University of Pennsylvania,Division of Endocrine and Oncologic Surgery, Department of Surgery, and the Rena Rowan Breast Center, Perelman School of Medicine
[2] University of Pennsylvania,Abramson Cancer Center, Perelman School of Medicine
[3] University of Pennsylvania,Thoracic Oncology Research Laboratory, Pulmonary Division, Perelman School of Medicine
[4] University of Pennsylvania,Department of Pathology and Lab Medicine, Perelman School of Medicine
[5] The Wistar Institute,Tumor Microenvironment and Metastasis Program
[6] Fox Chase Cancer Center,Abramson Family Cancer Research Institute, Perelman School of Medicine
[7] University of Pennsylvania,undefined
[8] Perelman Center for Advanced Medicine,undefined
来源
关键词
Mesothelin; Breast cancer subtypes; Triple negative breast cancer; Chimeric antigen receptor; Immunotherapy;
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学科分类号
摘要
Mesothelin is a cell-surface glycoprotein present on mesothelial cells and elicits T cell responses in a variety of cancers including pancreatic, biliary and ovarian cancer. Breast cancer is not known to express mesothelin. We postulated that mesothelin may be a unique tumor-associated antigen in triple negative breast cancer (TNBC), a less common breast cancer subtype which may have been under-represented in prior studies that characterized mesothelin expression. Therefore, we screened 99 primary breast cancer samples by immunohistochemistry analysis using formalin-fixed paraffin-embedded archival tumor tissues and confirmed that mesothelin was overexpressed in the majority of TNBC (67 %) but only rarely in <5 % ER(+) or Her2-neu(+) breast cancer, respectively. To determine whether mesothelin may be exploited as a novel immunotherapy target in breast cancer, an in vitro cell killing assay was performed to compare the ability of genetically modified T cells expressing a chimeric antibody receptor (CAR) specific for mesothelin (mesoCAR T cells) or non-transduced T cells to kill mesothelin-expressing primary breast cancer cells. A significantly higher anti-tumor cytotoxicity by mesoCAR T cells was observed (31.7 vs. 8.7 %, p < 0.001). Our results suggest that mesothelin has promise as a novel immunotherapy target for TNBC for which effective targeted therapy is lacking to date.
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页码:799 / 804
页数:5
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