PMID- 21938468 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20121002 LR - 20211020 IS - 0920-9069 (Print) IS - 1573-0778 (Electronic) IS - 0920-9069 (Linking) VI - 64 IP - 1 DP - 2012 Jan TI - Clinical reagents of GM-CSF and IFN-alpha induce the generation of functional chronic myeloid leukemia dendritic cells in vitro. PG - 75-81 LID - 10.1007/s10616-011-9393-2 [doi] AB - Dendritic cells (DCs) have been successfully induced in vitro from chronic myeloid leukemia (CML) cells, which may provide a promising immunotherapeutic protocol for CML. To facilitate the optimization of DCs-based vaccination protocols, we investigated the efficiency of in vitro generation of DCs from bone marrow mononuclear cells of CML patients by clinical reagents of GM-CSF and IFN-alpha. Bone marrow mononuclear cells were isolated from eight CML patients and CML-DCs were generated in the presence of different cytokines (Group A: GM-CSF for research and IL-4 for research; Group B: GM-CSF for injection and IFN-alpha for injection) in RMPI-1640 medium containing 10% human AB serum. After 8 days, the morphologic features of CML-DCs were observed and their immunophenotypes were analyzed by flow cytometry. The activity of CML-DCs was determined by evaluating their ability to stimulate allogeneic mixed lymphocyte reaction (allo-MLR) and anti-leukemic cytotoxic T lymphocytes (CTLs). The culture protocols were successful in generating functional CML-DCs from all the CML patients as evidenced by the significant upregulation of CD80, CD86, CD83 HLA-DR and CD1a compared to pre-cultured (p < 0.05), and increased allogeneic T cell stimulating proliferation capacity (p < 0.05). CML-DCs could stimulate a specific anti-leukemia response. In summary, we demonstrate that the combination of clinical reagents GM-CSF and IFN-alpha induced the generation of DCs that have the ability to stimulate a specific anti-leukemia CTLs response in vitro, indicating their feasibility for clinical vaccination protocols for CML patients. FAU - Weng, Kaizhi AU - Weng K AD - Zhangzhou Municipal Hospital, Affiliated to Fujian Medical University, Zhangzhou, 363000, People's Republic of China, lqlrandywkz@163.com. FAU - Xie, Xiaobao AU - Xie X FAU - Qiu, Guoqiang AU - Qiu G FAU - Gu, Weiying AU - Gu W LA - eng PT - Journal Article DEP - 20110922 PL - United States TA - Cytotechnology JT - Cytotechnology JID - 8807027 PMC - PMC3261453 EDAT- 2011/09/23 06:00 MHDA- 2011/09/23 06:01 PMCR- 2013/01/01 CRDT- 2011/09/23 06:00 PHST- 2011/06/04 00:00 [received] PHST- 2011/09/05 00:00 [accepted] PHST- 2011/09/23 06:00 [entrez] PHST- 2011/09/23 06:00 [pubmed] PHST- 2011/09/23 06:01 [medline] PHST- 2013/01/01 00:00 [pmc-release] AID - 9393 [pii] AID - 10.1007/s10616-011-9393-2 [doi] PST - ppublish SO - Cytotechnology. 2012 Jan;64(1):75-81. doi: 10.1007/s10616-011-9393-2. Epub 2011 Sep 22.