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Clinical outcomes of a novel therapeutic vaccine with Tax peptide‐pulsed dendritic cells for adult T cell leukaemia/lymphoma in a pilot study
Authors:Youko Suehiro  Atsuhiko Hasegawa  Tadafumi Iino  Amane Sasada  Nobukazu Watanabe  Masao Matsuoka  Ayako Takamori  Ryuji Tanosaki  Atae Utsunomiya  Ilseung Choi  Tetsuya Fukuda  Osamu Miura  Shigeo Takaishi  Takanori Teshima  Koichi Akashi  Mari Kannagi  Naokuni Uike  Jun Okamura
Affiliation:1. Department of Haematology, National Kyushu Cancer Centre, Fukuoka, Japan;2. Department of Immunotherapeutics, Tokyo Medical and Dental University, Tokyo, Japan;3. Centre for Advanced Medicine Innovation, Kyushu University, Fukuoka, Japan;4. Institute of Medical Science, University of Tokyo, Tokyo, Japan;5. Institute for Virus Research, Kyoto University, Kyoto, Japan;6. Clinical Laboratory Division, National Cancer Centre Hospital, Tokyo, Japan;7. Department of Haematology, Imamura Bun‐in Hospital, Kagoshima, Japan;8. Department of Haematology, Tokyo Medical and Dental University, Tokyo, Japan;9. Department of Haematology, Hokkaido University, Hokkaido, Japan;10. Department of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan;11. Institute for Clinical Research, National Kyushu Cancer Centre, Fukuoka, Japan
Abstract:Adult T cell leukaemia/lymphoma (ATL) is a human T cell leukaemia virus type‐I (HTLV‐I)‐infected T cell malignancy with poor prognosis. We herein developed a novel therapeutic vaccine designed to augment an HTLV‐I Tax‐specific cytotoxic T lymphocyte (CTL) response that has been implicated in anti‐ATL effects, and conducted a pilot study to investigate its safety and efficacy. Three previously treated ATL patients, classified as intermediate‐ to high‐risk, were subcutaneously administered with the vaccine, consisting of autologous dendritic cells (DCs) pulsed with Tax peptides corresponding to the CTL epitopes. In all patients, the performance status improved after vaccination without severe adverse events, and Tax‐specific CTL responses were observed with peaks at 16–20 weeks. Two patients achieved partial remission in the first 8 weeks, one of whom later achieved complete remission, maintaining their remission status without any additional chemotherapy 24 and 19 months after vaccination, respectively. The third patient, whose tumour cells lacked the ability to express Tax at biopsy, obtained stable disease in the first 8 weeks and later developed slowly progressive disease although additional therapy was not required for 14 months. The clinical outcomes of this pilot study indicate that the Tax peptide‐pulsed DC vaccine is a safe and promising immunotherapy for ATL.
Keywords:adult T cell leukaemia/lymphoma  tumour vaccine  dendritic cell  human T cell leukaemia virus type‐I  cytotoxic T lymphocyte
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