AML-loaded DC generate Th1-type cellular immune responses in vitro

Dongxia Xing, W. K. Decker, S. Li, S. N. Robinson, H. Yang, H. Segal, S. O'Connor, X. Yao, K. V. Komanduri, J. D. McMannis, R. B. Jones, M. de Lima, R. E. Champlin, E. J. Shpall

Research output: Contribution to journalArticlepeer-review

8 Scopus citations


Background: The generation of AML-specific T-lymphocyte responses by leukemia-derived DC has been documented by multiple investigators and is being pursued clinically. An obstacle to widespread use of this strategy is that it has not been possible to generate leukemic DC from all patients, and an alternative approach is needed if the majority of leukemia patients are to receive therapeutic vaccination in conjunction with other treatment protocols. Methods: In the present study, we generated DC from CD14-selected monocytes isolated from healthy donor PBPC and loaded them with a total cell lysate from AML patient blasts. Results: Immature in vitro -derived DC exhibited robust phagocytic activity, and mature DC demonstrated high expression of CD80, CD83, CD86 and the chemokine receptor CCR7, important for DC migration to local lymph nodes. Mature, Ag-loaded DC were used as APC for leukemia-specific cytotoxic T-lymphocyte (CTL) induction and demonstrated cytotoxic activity against leukemic targets. CTL lysis was Ag-specific, with killing of both allogeneic leukemic blasts and autologous DC loaded with allogeneic AML lysate. HLA-matched controls were not lysed in our system. Discussion: These data support further research into the use of this strategy as an alternative approach to leukemia-derived DC vaccination.

Original languageEnglish (US)
Pages (from-to)95-104
Number of pages10
Issue number2
StatePublished - May 2006
Externally publishedYes


  • Ag processing/presentation
  • AML
  • Cytotoxic T lymphocyte
  • DC

ASJC Scopus subject areas

  • Immunology
  • Immunology and Allergy
  • Pharmacology


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