Lymphocyte-conditioned medium in combination with interleukin-2 effectively induces antitumour autoimmunity by adoptive transfer of short activated killer (SHAK) cells.

Cytokines and molecular therapy Pub Date : 1995-03-01
J Buer, R Hilse, I Dallmann, J Grosse, H Kirchner, U Zorn, E L Hänninen, A Franzke, S Duensing, H Poliwoda
{"title":"Lymphocyte-conditioned medium in combination with interleukin-2 effectively induces antitumour autoimmunity by adoptive transfer of short activated killer (SHAK) cells.","authors":"J Buer,&nbsp;R Hilse,&nbsp;I Dallmann,&nbsp;J Grosse,&nbsp;H Kirchner,&nbsp;U Zorn,&nbsp;E L Hänninen,&nbsp;A Franzke,&nbsp;S Duensing,&nbsp;H Poliwoda","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, effective antitumour immunity was transferred by autologous short activated killer (SHAK) cells induced over four hours with lymphocyte conditioned medium (LCM) and recombinant interleukin-2 (rIL-2). Among eight patients with progressive metastatic renal cell carcinoma refractory to standard therapy, there were six objective tumour responses to SHAKs. Progression-free survival ranged from 0 to 8+ months, and overall survival ranged from 2 to 14+ months, with a median of 9+ months. Systemic toxicity of SHAKs was limited to flulike symptoms. Patient SHAKs provided a tumour-specific immunity, both cellular and humoral (expression and secretion of secondary cytokines, including IL-2, GM-CSF, INF-gamma and TNF-alpha), far superior to rIL-2 activated killer cells.</p>","PeriodicalId":79484,"journal":{"name":"Cytokines and molecular therapy","volume":"1 1","pages":"39-46"},"PeriodicalIF":0.0000,"publicationDate":"1995-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytokines and molecular therapy","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, effective antitumour immunity was transferred by autologous short activated killer (SHAK) cells induced over four hours with lymphocyte conditioned medium (LCM) and recombinant interleukin-2 (rIL-2). Among eight patients with progressive metastatic renal cell carcinoma refractory to standard therapy, there were six objective tumour responses to SHAKs. Progression-free survival ranged from 0 to 8+ months, and overall survival ranged from 2 to 14+ months, with a median of 9+ months. Systemic toxicity of SHAKs was limited to flulike symptoms. Patient SHAKs provided a tumour-specific immunity, both cellular and humoral (expression and secretion of secondary cytokines, including IL-2, GM-CSF, INF-gamma and TNF-alpha), far superior to rIL-2 activated killer cells.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
淋巴细胞条件培养基联合白细胞介素-2通过短激活杀伤(SHAK)细胞过继转移有效诱导抗肿瘤自身免疫。
在这项研究中,用淋巴细胞条件培养基(LCM)和重组白细胞介素-2 (il -2)诱导的自体短激活杀伤细胞(SHAK)在4小时内转移了有效的抗肿瘤免疫。在8例标准治疗难治性进展性转移性肾癌患者中,有6例患者对SHAKs有客观肿瘤反应。无进展生存期为0 ~ 8个月,总生存期为2 ~ 14个月,中位生存期为9个月以上。SHAKs的全身毒性仅限于流感样症状。患者SHAKs提供了肿瘤特异性免疫,包括细胞和体液(次级细胞因子的表达和分泌,包括IL-2, GM-CSF, inf - γ和tnf - α),远远优于IL-2激活的杀伤细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Long-term interleukin-3 and intensive immunosuppression in the treatment of aplastic anemia. Stem cell factor and PIXY-321 in acute lymphoblastic leukemia: in vitro study on proliferative effects and apoptosis. Idiotype vaccination strategies against a murine B-cell lymphoma: dendritic cells loaded with idiotype and bispecific idiotype x anti-class II antibodies can protect against tumor growth. Polymorphism within the second intron of the IL-1 receptor antagonist gene in patients with hematopoietic malignancies. Soluble tumor necrosis factor (sTNF) receptors: a possible prognostic marker for bone marrow transplantation-related complications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1