High dose RHAMM-R3 peptide vaccination for patients with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) and multiple myeloma (MM)

نویسندگان

  • Jochen Greiner
  • Anita Schmitt
  • Krzysztof Giannopoulos
  • Markus T. Rojewski
  • Marlies Goetz
  • Isabel Funk
  • Mark Ringhoffer
  • Donald Bunjes
  • Susanne Hofmann
  • Gerd Ritter
  • Hartmut Doehner
  • Michael Schmitt
  • Marlies Götz
  • Hartmut Döhner
  • José Carreras Leu
چکیده

Background: Recently, we demonstrated immunological and clinical responses to a RHAMM-R3 peptide vaccine in patients with acute myeloid leukemia, myelodysplastic syndrome (MDS) and multiple myeloma (MM). To improve the outcome of the vaccine, a second cohort was vaccinated with a higher dose of 1,000μg peptide. Design and Methods: Nine patients received four vaccinations subcutaneously at a biweekly interval. Immunomonitoring of cytotoxic CD8+ as well as regulatory CD4+ T cells was performed by flow cytometry as well as by enzyme-linked immunospot (ELISpot) assays. Parameters of clinical response were assessed. Results: In four of nine patients (44%) we detected positive immunological responses. These patients showed an increase of CD8+RHAMM-R3_tetramer+/ CD45RA+/CCR7-/CD27-/CD28effector T cells and an increase of R3-specific CD8+ T cells. Two of these patients showed a significant decrease of regulatory T cells (Tregs). In one patient without response Tregs frequency increased from 5 to 16%. Three patients showed clinical effects: One patient with MDS RAEB-1 showed a reduction of leukemic blasts in the bone marrow, another MDS patient an improvement of peripheral blood counts and one patient with MM a reduction of free light chains. In comparison with the 300 μg cohort clinical and immunological reactions were lower in this cohort. Conclusions: High dose RHAMM-R3 peptide vaccination induced immunological responses and positive clinical effects. Therefore, RHAMM constitutes a promising structure for further targeted immunotherapies in patients with different hematological malignancies. However, higher doses of peptide did not improve the frequency and intensity of immune responses in this trial. (This study is registered at http://ISRCTN.org as ISRCTN32763606) DOI: 10.3324/haematol.2009.014704

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RHAMM-R3 peptide vaccination in patients with acute myeloid leukemia, myelodysplastic syndrome, and multiple myeloma elicits immunologic and clinical responses.

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تاریخ انتشار 2010