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Bioactivity of umbilical cord blood dendritic cells and anti-leukemia effect.
Wei, Xu-Cang; Yang, Di-Di; Han, Xiu-Rui; Zhao, Yu-An; Li, Yan-Chun; Zhang, Li-Jie; Wang, Jiu-Ju.
Afiliação
  • Wei XC; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Yang DD; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Han XR; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Zhao YA; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Li YC; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Zhang LJ; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
  • Wang JJ; Institute of Hematological Research, Shaanxi Provincial People's Hospital Xi'an 710068.
Int J Clin Exp Med ; 8(10): 19725-30, 2015.
Article em En | MEDLINE | ID: mdl-26770637
ABSTRACT

OBJECTIVE:

We investigated the effect of umbilical cord blood dendritic cells (DCs) on in vitro proliferation, immunophenotypes and levels of homologous cytokine-induced killer cells (CIK) and the toxicity on leukemia cells.

METHOD:

Mononuclear cell-induced DC-CIK cells derived from umbilical cord blood were collected and co-cultured in the proportion of 15. Cord blood CIK cells or peripheral blood DC-CIK cells were used as control. Phenotypes were analyzed by flow cytometry; vial cell counting was performed using trypan blue, and the killing activity of effector cells against leukemia cells was measured by MTT assay. The levels of interferon-r (IFN-r), tumor necrosis factor-a (TNF-α) and interleukin-12 (IL-12) were determined by ELISA.

RESULTS:

The proliferative capacity of DC-CIK cells was obviously improved compared with cord blood CIK cells and peripheral blood DC-CIK cells (P<0.05, P<0.05). During the co-culture of cord blood DC-CIK cells, the ratios of CD 3 (+) CD 8 (+) and CD 3 (+) CD 56 (+) cells were obviously higher than that of CIK cells under the same conditions (P<0.05). On day 3 of co-culture, the levels of IL-12, IFN-r and TNF-a in cultured supernatant of cord blood DC-CIK cells were all higher than those secreted by CIK cells cultured alone (P<0.01, P<0.05, P<0.05). When the effector to target ratio was 2.5-201, the killing effect of cord blood DC-CIK cells against each subtype of acute leukemia cells was obviously higher than that of CIK cells (P<0.05). No significant differences in killing effect were observed for different subtypes. This finding was consistent with the killing effect of peripheral blood DC-CIK cells against leukemia cells.

CONCLUSION:

Cord blood DCs can enhance the proliferative capacity of homologous CIK cells and its anti-leukemia effect. Though cord blood DC-CIK cells showed a higher proliferative capacity than peripheral blood DC-CIK cells, the two types of DC-CIK cells did not differ significantly in terms of cytoxicity. With a high availability and the low probability of graft rejection reaction, cord blood DC-CIK cells have a brighter prospect for application in immunotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Clin Exp Med Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Clin Exp Med Ano de publicação: 2015 Tipo de documento: Article