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Naturally acquired MAGE-A10- and SSX-2-specific CD8+ T cell responses in patients with hepatocellular carcinoma.

作者信息

Bricard Gabriel, Bouzourene Hanifa, Martinet Olivier, Rimoldi Donata, Halkic Nermin, Gillet Michel, Chaubert Pascal, Macdonald H Robson, Romero Pedro, Cerottini Jean-Charles, Speiser Daniel E

机构信息

Division of Clinical Onco-Immunology, Ludwig Institute for Cancer Research, Lausanne, Switzerland.

出版信息

J Immunol. 2005 Feb 1;174(3):1709-16. doi: 10.4049/jimmunol.174.3.1709.


DOI:10.4049/jimmunol.174.3.1709
PMID:15661935
Abstract

Immunotherapy is being proposed to treat patients with hepatocellular carcinoma (HCC). However, more detailed knowledge on tumor Ag expression and specific immune cells is required for the preparation of highly targeted vaccines. HCC express a variety of tumor-specific Ags, raising the question whether CTL specific for such Ags exist in HCC patients. Indeed, a recent study revealed CTLs specific for two cancer-testis (CT) Ags (MAGE-A1 and MAGE-A3) in tumor infiltrating lymphocytes of HCC patients. Here we assessed the presence of T cells specific for additional CT Ags: MAGE-A10, SSX-2, NY-ESO-1, and LAGE-1, which are naturally immunogenic as demonstrated in HLA-A2(+) melanoma patients. In two of six HLA-A2(+) HCC patients, we found that MAGE-A10- and/or SSX-2-specific CD8(+) T cells naturally responded to the disease, because they were enriched in tumor lesions but not in nontumoral liver. Isolated T cells specifically and strongly killed tumor cells in vitro, providing evidence that these CTL were selected in vivo for high avidity Ag recognition. Therefore, besides melanoma, HCC is the second solid human tumor with clear evidence for in vivo tumor recognition by T cells, providing the rational for specific immunotherapy, based on immunization with CT Ags such as MAGE-A10 and SSX-2.

摘要

相似文献

[1]
Naturally acquired MAGE-A10- and SSX-2-specific CD8+ T cell responses in patients with hepatocellular carcinoma.

J Immunol. 2005-2-1

[2]
Tumor-reactive, SSX-2-specific CD8+ T cells are selectively expanded during immune responses to antigen-expressing tumors in melanoma patients.

Cancer Res. 2003-9-1

[3]
The spontaneous CD8+ T-cell response to HLA-A2-restricted NY-ESO-1b peptide in hepatocellular carcinoma patients.

Clin Cancer Res. 2004-10-15

[4]
Proteasome-assisted identification of a SSX-2-derived epitope recognized by tumor-reactive CTL infiltrating metastatic melanoma.

J Immunol. 2002-2-15

[5]
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[6]
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J Immunol. 2000-12-15

[7]
[Estimation of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8+T cells in vitro induced by HLA-A2 restricted NY-ESO-1b peptide].

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[8]
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[9]
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[10]
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引用本文的文献

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J Exp Clin Cancer Res. 2024-3-20

[2]
Systemic T-cell and humoral responses against cancer testis antigens in hepatocellular carcinoma patients.

Oncoimmunology. 2022

[3]
Novel Nanotechnology Approaches to Overcome Drug Resistance in the Treatment of Hepatocellular Carcinoma: Glypican 3 as a Useful Target for Innovative Therapies.

Int J Mol Sci. 2022-9-2

[4]
Therapeutic Vaccines against Hepatocellular Carcinoma in the Immune Checkpoint Inhibitor Era: Time for Neoantigens?

Int J Mol Sci. 2022-2-11

[5]
Novel TCR-like CAR-T cells targeting an HLA∗0201-restricted SSX2 epitope display strong activity against acute myeloid leukemia.

Mol Ther Methods Clin Dev. 2021-10-1

[6]
Natural Killer Cells and T Cells in Hepatocellular Carcinoma and Viral Hepatitis: Current Status and Perspectives for Future Immunotherapeutic Approaches.

Cells. 2021-5-28

[7]
Expression of Cancer Testis Antigens in Tumor-Adjacent Normal Liver Is Associated with Post-Resection Recurrence of Hepatocellular Carcinoma.

Cancers (Basel). 2021-5-20

[8]
KK-LC-1 may be an effective prognostic biomarker for gastric cancer.

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[9]
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Clin Sarcoma Res. 2020-2-4

[10]
Immune cell therapy for hepatocellular carcinoma.

J Hematol Oncol. 2019-5-29

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