| Literature DB >> 28105230 |
Yanfeng Liu1, Haibo Liu2, Hausheng Liu2, Pengcheng He2, Jing Li2, Xin Liu2, Limei Chen2, Mengchang Wang2, Jiejing Xi2, Huaiyu Wang2, Haitao Zhang2, Ying Zhu3, Wei Zhu3, Jing Ning3, Caili Guo3, Chunhong Sun3, Mei Zhang2.
Abstract
Individuals >65 years old account for a large proportion of cancer patients, and usually have poor prognoses due to relative weaker physiological function and lower drug tolerance. To characterize the efficacy and safety of dendritic cell (DC)-activated cytokine-induced killer cell (CIK)-mediated treatment, and develop an adoptive immunotherapy for cancer patients >65 years old, a retrospective study was performed in 58 cancer sufferers who received 1-4 cycles of DC-activated CIK (DC-CIK) treatment and evaluated the response (tumor remission rate) and toxicity (side effects to the treatment). The present results showed that DCs and CIKs could be expanded rapidly in vitro, and following co-culture with DCs, the population of cluster of differentiation (CD) 3+, CD3+CD4+, CD3+CD8+ and CD3+CD56+ CIKs was significantly increased compared to CIKs without DC activation (P=0.044). In addition, DC-CIK infusion produced marked clinical outcomes, resulting in an objective remission rate, overall clinical benefit rate and Karnofsky performance status of 44.83, 75.86 and 87.28±5.46%, respectively, which was significantly improved compared with prior to treatment (P<0.05). Additionally, subsequent to two cycles of this immunotherapy, several tumor marker expression levels declined, returning to the normal range. The proportion of CD3+CD4+ (P=0.017) and CD3+CD8+ (P=0.023) lymphocytes, and the population of CD4/CD8 cells (P=0.024) were also increased. In conclusion, the present study suggests that the immunotherapy mediated by DC-CIK is safe and effective for cancer patients aged >65 years.Entities:
Keywords: cancer; cytokine-induced killer cells; dendritic cells; immunotherapy
Year: 2016 PMID: 28105230 PMCID: PMC5228401 DOI: 10.3892/ol.2016.5337
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967