Adoptive transfer of autologous, HER2-specific, cytotoxic T lymphocytes for the treatment of HER2-overexpressing breast cancer

被引:115
作者
Bernhard, Helga
Neudorfer, Julia
Gebhard, Kerstin
Conrad, Heinke
Hermann, Christine
Naehrig, Joerg
Fend, Falko
Weber, Wolfgang
Busch, Dirk H.
Peschel, Christian
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Med 3, D-81675 Munich, Germany
[2] Tech Univ Munich, Klinikum Rechts Isar, Dept Hematol Oncol, D-81675 Munich, Germany
[3] Tech Univ Munich, Klinikum Rechts Isar, Dept Pathol, D-81675 Munich, Germany
[4] Tech Univ Munich, Klinikum Rechts Isar, Dept Nucl Med, D-81675 Munich, Germany
[5] Neuherberg & Tech Univ Munich, Inst Hlth & Environm, GSF, Clin Cooperat Grp Antigen Specif Immunotherapy, Neuherberg, Germany
[6] Tech Univ Munich, Klinikum Rechts Isar, Dept Microbiol Immunol & Hygiene, D-81675 Munich, Germany
关键词
tumor immunity; human; cytotoxic T cells; antigens; peptides; epitopes; MHC; IN-VIVO PERSISTENCE; CELL TRANSFER THERAPY; MELANOMA PATIENTS; HER-2/NEU PROTOONCOGENE; BONE-MARROW; TUMOR; ANTIGEN; CLONES; GENERATION; REGRESSION;
D O I
10.1007/s00262-007-0355-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human epidermal growth factor receptor 2 (HER2) has been targeted as a breast cancer-associated antigen by immunotherapeutical approaches based on HER2-directed monoclonal antibodies and cancer vaccines. We describe the adoptive transfer of autologous HER2-specific T-lymphocyte clones to a patient with metastatic HER2-overexpressing breast cancer. The HLA/multimer-based monitoring of the transferred T lymphocytes revealed that the T cells rapidly disappeared from the peripheral blood. The imaging studies indicated that the T cells accumulated in the bone marrow (BM) and migrated to the liver, but were unable to penetrate into the solid metastases. The disseminated tumor cells in the BM disappeared after the completion of adoptive T-cell therapy. This study suggests the therapeutic potential for HER2-specific T cells for eliminating disseminated HER2-positive tumor cells and proposes the combination of T cell-based therapies with strategies targeting the tumor stroma to improve T-cell infiltration into solid tumors.
引用
收藏
页码:271 / 280
页数:10
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