TY - JOUR
T1 - Clinical outcomes of a novel therapeutic vaccine with Tax peptide-pulsed dendritic cells for adult T cell leukaemia/lymphoma in a pilot study
AU - Suehiro, Youko
AU - Hasegawa, Atsuhiko
AU - Iino, Tadafumi
AU - Sasada, Amane
AU - Watanabe, Nobukazu
AU - Matsuoka, Masao
AU - Takamori, Ayako
AU - Tanosaki, Ryuji
AU - Utsunomiya, Atae
AU - Choi, Ilseung
AU - Fukuda, Tetsuya
AU - Miura, Osamu
AU - Takaishi, Shigeo
AU - Teshima, Takanori
AU - Akashi, Koichi
AU - Kannagi, Mari
AU - Uike, Naokuni
AU - Okamura, Jun
N1 - Publisher Copyright:
© 2015 John Wiley & Sons Ltd.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - 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.
AB - 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.
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U2 - 10.1111/bjh.13302
DO - 10.1111/bjh.13302
M3 - Article
C2 - 25612920
AN - SCOPUS:84927694937
SN - 0007-1048
VL - 169
SP - 356
EP - 367
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 3
ER -