Literature DB >> 16525677

Postoperative immunosuppression cascade and immunotherapy using lymphokine-activated killer cells for patients with esophageal cancer: possible application for compensatory anti-inflammatory response syndrome.

Yoshiyuki Yamaguchi1, Jun Hihara, Katsuji Hironaka, Akiko Ohshita, Riki Okita, Makoto Okawaki, Kazuo Matsuura, Ichiro Nagamine, Takuhiro Ikeda, Masahiro Ohara, Yoichi Hamai.   

Abstract

Immunological parameters were measured in order to elucidate a postoperative immunosuppression mechanism in transthoracic esophagectomy for patients with esophageal cancer. Moreover, lymphokine-activated killer (LAK) cells were transferred just after the surgery to overcome the postoperative immunosuppression. Fifteen consecutive patients who underwent transthoracic esophagectomy were subjected to the postoperative measurement of immunological parameters. Ten patients who underwent open cholecystectomy served as controls. Heparinized venous blood was obtained pre- and postoperatively, and serum levels of cytokines IL-6 and IL-10 and immunosuppressive acidic protein (IAP) were measured. Peripheral blood lymphocytes were harvested and analyzed by flow cytometry for phenotype detection and by a mixed lymphocyte reaction for detecting concanavalin (Con)-A-induced or -non-induced suppressor activity. Another 29 consecutive patients who underwent transthoracic esophagectomy were randomly enrolled in a postoperative immunotherapy trial either with or without lymphokine-activated killer cells. It was found that, in the esophagectomy group, IL-6 and IL-10 increased postoperatively and peaked on day 1, followed by an increase in IAP, peaked again on day 4, with a profound decrease in helper and cytotoxic T-cell subsets, followed by increases in Con-A-induced (on day 7 or later) and spontaneous (on day 10) suppressor activities. These changes were minimal in the cholecystectomy group. LAK cell transfer restored the postoperative decrease in the helper and cytotoxic T-cell population, and there was a trend of reduction for postoperative remote infection such as pneumonia and surgical site infection in the LAK therapy group. Taken together, we would like to propose the existence of a postoperative immunosuppression cascade consisting of increases in cytokines and immunosuppressive proteins, decreases in helper and cytotoxic T-cell populations, and the development of suppressor T-cell activities in surgery for esophageal cancer. Postoperative adoptive transfer of LAK cells may be a novel clinical application in surgery for esophageal cancer as a means of treating this postoperative immunosuppressive condition that may be identical to the status of compensatory anti-inflammatory response syndrome (CARS).

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Year:  2006        PMID: 16525677

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  9 in total

1.  Cancer Recurrence After Esophagectomy: Impact of Postoperative Infection in Propensity-Matched Cohorts.

Authors:  Vernissia Tam; James D Luketich; Daniel G Winger; Inderpal S Sarkaria; Ryan M Levy; Neil A Christie; Omar Awais; Manisha R Shende; Katie S Nason
Journal:  Ann Thorac Surg       Date:  2016-06-25       Impact factor: 4.330

2.  Preoperative therapy of esophagogastric cancer: the problem of nonresponding patients.

Authors:  S Blank; A Stange; L Sisic; W Roth; L Grenacher; F Sterzing; M Burian; D Jäger; M Büchler; K Ott
Journal:  Langenbecks Arch Surg       Date:  2012-12-07       Impact factor: 3.445

3.  Immunological changes after minimally invasive or conventional esophageal resection for cancer: a randomized trial.

Authors:  K W Maas; S S A Y Biere; I M W van Hoogstraten; D L van der Peet; M A Cuesta
Journal:  World J Surg       Date:  2014-01       Impact factor: 3.352

Review 4.  Regulating surgical oncotaxis to improve the outcomes in cancer patients.

Authors:  Toshihiro Hirai; Hideo Matsumoto; Hisako Kubota; Yoshiyuki Yamaguchi
Journal:  Surg Today       Date:  2013-06-05       Impact factor: 2.549

5.  BRD7 plays an anti-inflammatory role during early acute inflammation by inhibiting activation of the NF-кB signaling pathway.

Authors:  Ran Zhao; Yukun Liu; Heran Wang; Jing Yang; Weihong Niu; Songqing Fan; Wei Xiong; Jian Ma; Xiaoling Li; Joshua B Phillips; Ming Tan; Yuanzheng Qiu; Guiyuan Li; Ming Zhou
Journal:  Cell Mol Immunol       Date:  2016-07-04       Impact factor: 11.530

6.  Influence of transfusion of lymphokine-activated T killer cells on inflammatory responses in dogs after laparotomy.

Authors:  Keiichiro Mie; Mizuki Tomihari; Kiyotaka Hoshi; Takashi Nakamura; Tomohiro Yamaguchi; Kazuro Miyahara; Terumasa Shimada
Journal:  J Vet Med Sci       Date:  2016-01-02       Impact factor: 1.267

7.  Adenoviral-based immunotherapy provides local disease control in an orthotopic murine model of esophageal cancer.

Authors:  Jon G Quatromoni; Jarrod D Predina; Pratik Bhojnagarwala; Ryan P Judy; Jack Jiang; Elizabeth M De Jesus; Veena Kapoor; Guanjun Cheng; Olugbenga T Okusanya; Evgeniy Eruslanov; Sunil Singhal
Journal:  J Immunother       Date:  2014-06       Impact factor: 4.456

8.  Preventive effect of ulinastatin on postoperative complications, immunosuppression, and recurrence in esophagectomy patients.

Authors:  Lingmin Zhang; Ning Wang; Suna Zhou; Wenguang Ye; Qinglin Yao; Guixia Jing; Mingxin Zhang
Journal:  World J Surg Oncol       Date:  2013-04-10       Impact factor: 2.754

9.  Clinical applications of dendritic cells-cytokine-induced killer cells mediated immunotherapy for pancreatic cancer: an up-to-date meta-analysis.

Authors:  Yucai Zhang; Xiaorui Zhang; Anqi Zhang; Ke Li; Kai Qu
Journal:  Onco Targets Ther       Date:  2017-08-23       Impact factor: 4.147

  9 in total

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