AI Article Synopsis

  • Adult T cell leukaemia/lymphoma (ATL) is a serious cancer caused by the human T cell leukaemia virus type-I (HTLV-I) that has a poor prognosis.
  • A new therapeutic vaccine was developed to enhance the immune response specifically targeting HTLV-I Tax proteins, and a pilot study was conducted on three high-risk ATL patients.
  • All patients showed improved health after vaccination, with two experiencing partial or complete remission, while the third had stable disease for 14 months, suggesting the vaccine is a safe and promising treatment option for ATL.

Article 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.

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Source
http://dx.doi.org/10.1111/bjh.13302DOI Listing

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