Literature DB >> 28941416

Increased cycles of DC/CIK immunotherapy decreases frequency of Tregs in patients with resected NSCLC.

Haiping Song1, Shujuan Liu1, Ziyun Zhao2, Weihong Sun3, Xiaofang Wei4, Xuezhen Ma5, Peng Zhao4, Daiqing Gao4.   

Abstract

Regulatory T cells (Tregs) suppress antitumor immune responses. Cycles of Dendritic cells (DC) vaccination combined with cytokine-induced killer (CIK) cells (DC/CIK) treatment were significantly related with good prognosis. Therefore, we investigated whether increased cycles of immunotherapy could decrease frequency of Tregs in patients with resected non-small cell lung cancer (NSCLC). Previous study from our laboratory has determined that the optimal cutoff point of the cycle count was 3cycles. We examined the levels of Tregs and the related cytokines by flow cytometric and cytokine analysis in these patients after more than (≥) 3cycles or less than (<) 3cycles of DC/CIK cell treatment. Significant reduction of Tregs frequency, Treg-generated cytokines level and recurrence rate were presented in patients received with ≥3cycles of DC/CIK cell treatment compared with patients with <3cycles of treatment. Interestingly, Tregs frequency and the related cytokines level were similar between patients suffered tumor recurrence and patients without recurrence in both groups. Together, our findings reveal that increased cycle count of DC/CIK cell immunotherapy contribute to decline of Tregs frequency and cancer recurrence rate in patients with resected NSCLC.
Copyright © 2017. Published by Elsevier B.V.

Entities:  

Keywords:  Cytokine-induced killer cell; Dendritic cell; Foxp3(+) Treg cells; Immunotherapy; Non-small cell lung cancer

Mesh:

Substances:

Year:  2017        PMID: 28941416     DOI: 10.1016/j.intimp.2017.09.014

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  8 in total

1.  Cytokine-induced killer cells co-cultured with non-cell derived targeting peptide-loaded dendritic cells induce a specific antitumor response.

Authors:  Cuijuan Liu; Xueyuan Cui; Dayong Zhou; Chunlin Li; Mengya Zhao; Yaqing Jin; Chen Ding; Yimin Zhu
Journal:  Cancer Biol Ther       Date:  2019-02-19       Impact factor: 4.742

Review 2.  NK and cells with NK-like activities in cancer immunotherapy-clinical perspectives.

Authors:  Keywan Mortezaee; Jamal Majidpoor
Journal:  Med Oncol       Date:  2022-06-18       Impact factor: 3.064

3.  18F-FHBG PET-CT Reporter Gene Imaging of Adoptive CIK Cell Transfer Immunotherapy for Breast Cancer in a Mouse Model.

Authors:  Xiaofeng Li; Guotao Yin; Wei Ji; Jianjing Liu; Yufan Zhang; Jian Wang; Xiang Zhu; Lei Zhu; Dong Dai; Wenchao Ma; Wengui Xu
Journal:  Onco Targets Ther       Date:  2020-11-13       Impact factor: 4.147

4.  Efficacy of DC-CIK-based immunotherapy combined with chemotherapy in the treatment of intermediate to advanced non-small cell lung cancer.

Authors:  Ling Wang; Yue Dai; Fuliang Zhu; Zhimin Qiu; Yaqi Wang; Yinghui Hu
Journal:  Am J Transl Res       Date:  2021-11-15       Impact factor: 4.060

5.  Role of CD200/CD200R Signaling Pathway in Regulation of CD4+T Cell Subsets During Thermal Ablation of Hepatocellular Carcinoma.

Authors:  Shengchuan Huang; Yan Pan; Qingdong Zhang; Weiping Sun
Journal:  Med Sci Monit       Date:  2019-03-06

Review 6.  Impaired dendritic cell functions in lung cancer: a review of recent advances and future perspectives.

Authors:  Jing-Bo Wang; Xue Huang; Fu-Rong Li
Journal:  Cancer Commun (Lond)       Date:  2019-07-15

Review 7.  Dendritic Cell-Based Immunotherapy in Lung Cancer.

Authors:  Dieter Stevens; Joline Ingels; Sandra Van Lint; Bart Vandekerckhove; Karim Vermaelen
Journal:  Front Immunol       Date:  2021-02-12       Impact factor: 7.561

8.  Lack of sphingomyelin synthase 2 reduces cerebral ischemia/reperfusion injury by inhibiting microglial inflammation in mice.

Authors:  Yu Yang; Fengxian Hu; Guifeng Yang; Qingmei Meng
Journal:  Exp Ther Med       Date:  2020-10-22       Impact factor: 2.447

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.