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Identification of Claudin 6-specific HLA class I- and HLA class II-restricted T cell receptors for cellular immunotherapy in ovarian cancer
Adoptive cell therapy (ACT) is one of promising immunotherapies for cancer patients by providing a large amount of cancer antigen-specific effector T cells that can be manufactured rapidly by ex vivo gene engineering. To provide antigen-specificity to patients' autologous T cells in a short-ter...
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Published in: | Oncoimmunology 2022-12, Vol.11 (1), p.2020983-2020983 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Adoptive cell therapy (ACT) is one of promising immunotherapies for cancer patients by providing a large amount of cancer antigen-specific effector T cells that can be manufactured rapidly by ex vivo gene engineering. To provide antigen-specificity to patients' autologous T cells in a short-term culture, T-cell receptors (TCRs) or chimeric antigen receptors (CARs) are transduced to bulk T cells. Because of intra- and inter-tumoral heterogeneity in tumor antigen expression, a repertoire of TCR or CAR genes targeting a wide range of tumor antigens are required for a broad and effective treatment by ACT. Here, we characterized immunogenicity of claudin 6 (CLDN6) in ovarian cancer patients and identified specific TCR genes from CD8
+
and CD4
+
T cells. CLDN6 protein was frequently expressed on EpCAM
+
ovarian cancer cells but not CD45
+
lymphocytes in tumor ascites of ovarian cancer patients. Spontaneous CLDN6-specific CD4
+
and CD8
+
T-cell response was detected in peripheral blood mononuclear cells (PBMCs) from 1 out of 17 ovarian cancer patients. HLA-A*02:01 (A2) and DR*04:04 (DR4)-restricted TCR genes were isolated from CLDN6-specific CD8
+
and CD4
+
T cells, respectively. T cells that were engineered with A2-restricted TCR gene recognized and killed A2
+
CLDN6
+
cancer cells. DR4-restricted TCR-transduced T cells directly recognized DR4
+
CLDN6
+
-overexpressed cancer cells. Our results demonstrate that these CLDN6-specific TCR genes are useful as therapeutic genes for ACT to patients with ovarian and other solid tumors expressing CLDN6. |
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ISSN: | 2162-402X 2162-4011 2162-402X |
DOI: | 10.1080/2162402X.2021.2020983 |