TY - JOUR
T1 - Inhibitory molecules expressed in T lymphocytes in patients with lung cancer before and after chemotherapy
AU - Xu, Yujie
AU - Zhang, Yi
AU - Kuang, Xiankui
AU - Duan, Xiufang
AU - Li, Jieyao
AU - Li, Jianbin
AU - Zhang, Zhen
AU - Zhang, Bin
AU - Wang, Liping
PY - 2013/8/30
Y1 - 2013/8/30
N2 - Objective: The tumongenesis, progression, and metastasis of lung cancer are mostly governed by the immunosuppressive profile. This study aimed to explore the levels of various immunosuppressive inhibitory molecules in lung-cancer patients subjected to different chemotherapy cycles. Methods: Thirty-three patients with advanced lung cancer (ALC; stages III-IV) without receiving prior chemotherapy and 23 healthy subjects were enrolled in our study. Peripheral blood samples were collected from the patients before each chemotherapy cycle. The inhibitory markers expressed in T cells such as TIM3, PD-1, and CTLA4 were analyzed by flow cytometry. Results: The percentages of CD4+ T1M3+, CD8+ TIM3\ CD4+ PD-1+, CD8+ PD-1+, CD4+ CTLA-4+, and CD8+ CTLA-4+ T cells in the peripheral blood of the ALC patients were significantly higher compared to the controls. The percentage of CD4+ TIM3+, CD8+ TIM3+, CD4 + PD-1+, and CD8+ PD-1+ T lymphocytes in the peripheral blood of patients (n=19) who achieved PR or SD significantly decreased after five cycles of chemotherapy (PO.05). Similarly, the percentages of CD4+ CTLA-4+ and CD8 +CTLA-4+ T cells in the patients also decreased after five cycles of treatment. Conclusion: The immune status of ALC patients was evidently suppressed. Effective chemotherapy successfully potentiated effective immune responses by downregulating inhibitory molecules in T cells.
AB - Objective: The tumongenesis, progression, and metastasis of lung cancer are mostly governed by the immunosuppressive profile. This study aimed to explore the levels of various immunosuppressive inhibitory molecules in lung-cancer patients subjected to different chemotherapy cycles. Methods: Thirty-three patients with advanced lung cancer (ALC; stages III-IV) without receiving prior chemotherapy and 23 healthy subjects were enrolled in our study. Peripheral blood samples were collected from the patients before each chemotherapy cycle. The inhibitory markers expressed in T cells such as TIM3, PD-1, and CTLA4 were analyzed by flow cytometry. Results: The percentages of CD4+ T1M3+, CD8+ TIM3\ CD4+ PD-1+, CD8+ PD-1+, CD4+ CTLA-4+, and CD8+ CTLA-4+ T cells in the peripheral blood of the ALC patients were significantly higher compared to the controls. The percentage of CD4+ TIM3+, CD8+ TIM3+, CD4 + PD-1+, and CD8+ PD-1+ T lymphocytes in the peripheral blood of patients (n=19) who achieved PR or SD significantly decreased after five cycles of chemotherapy (PO.05). Similarly, the percentages of CD4+ CTLA-4+ and CD8 +CTLA-4+ T cells in the patients also decreased after five cycles of treatment. Conclusion: The immune status of ALC patients was evidently suppressed. Effective chemotherapy successfully potentiated effective immune responses by downregulating inhibitory molecules in T cells.
KW - Advanced lung cancer
KW - Chemotherapy
KW - Flow cytometry
KW - Inhibitory molecule
KW - T cell
UR - http://www.scopus.com/inward/record.url?scp=84887001543&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84887001543&partnerID=8YFLogxK
U2 - 10.3969/j.issn.1000-8179.20130292
DO - 10.3969/j.issn.1000-8179.20130292
M3 - Article
AN - SCOPUS:84887001543
SN - 1672-7118
VL - 40
SP - 960
EP - 964
JO - Chinese Journal of Clinical Oncology
JF - Chinese Journal of Clinical Oncology
IS - 16
ER -