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Antitumour actions of interferons: implications for cancer therapy.干扰素的抗肿瘤作用:对癌症治疗的启示。
Nat Rev Cancer. 2016 Mar;16(3):131-44. doi: 10.1038/nrc.2016.14.
2
Hepatitis C virus-specific cytotoxic T cell response restoration after treatment-induced hepatitis C virus control.治疗诱导的丙型肝炎病毒得到控制后丙型肝炎病毒特异性细胞毒性T细胞反应的恢复
World J Gastroenterol. 2015 Mar 28;21(12):3480-91. doi: 10.3748/wjg.v21.i12.3480.
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Helper T lymphocyte response in the peripheral blood of patients with intraepithelial neoplasia submitted to immunotherapy with pegylated interferon-α.接受聚乙二醇化干扰素-α免疫治疗的上皮内瘤变患者外周血中辅助性T淋巴细胞反应。
Int J Mol Sci. 2015 Mar 10;16(3):5497-509. doi: 10.3390/ijms16035497.
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An evaluation of immune system cell infiltrate in the cervical stroma of patients with grade III cervical intraepithelial neoplasia after treatment with intralesional alpha-2B interferon.对经病灶内注射α-2B干扰素治疗的III级宫颈上皮内瘤变患者宫颈基质中免疫系统细胞浸润情况的评估。
Eur J Gynaecol Oncol. 2014;35(1):20-5.
5
Immunomodulatory effects of interferons in malignancies.干扰素在恶性肿瘤中的免疫调节作用。
J Interferon Cytokine Res. 2013 Apr;33(4):154-61. doi: 10.1089/jir.2012.0167.
6
A new mechanism of action for the anticancer drug mitomycin C: mechanism-based inhibition of thioredoxin reductase.一种新型抗癌药物丝裂霉素 C 的作用机制:基于机制的硫氧还蛋白还原酶抑制作用。
Chem Res Toxicol. 2012 Jul 16;25(7):1502-11. doi: 10.1021/tx3002065. Epub 2012 Jun 25.
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Modulation of T-cell function by type I interferon.I 型干扰素对 T 细胞功能的调节。
Immunol Cell Biol. 2012 May;90(5):492-7. doi: 10.1038/icb.2012.7. Epub 2012 Mar 6.
8
Expression of cytokines in cervical stroma in patients with high-grade cervical intraepithelial neoplasia after treatment with intralesional interferon alpha-2b.病灶内注射α-2b干扰素治疗后高级别宫颈上皮内瘤变患者宫颈基质中细胞因子的表达
Eur J Gynaecol Oncol. 2010;31(5):522-9.
9
Topical interferon alpha 2b eye-drops for treatment of ocular surface squamous neoplasia: a dose comparison study.局部应用干扰素 alpha 2b 滴眼剂治疗眼表面鳞状上皮肿瘤:剂量比较研究。
Br J Ophthalmol. 2010 May;94(5):551-4. doi: 10.1136/bjo.2008.153197. Epub 2009 Jun 2.
10
Mechanisms of action of interferon and ribavirin in chronic hepatitis C: Summary of a workshop.干扰素与利巴韦林治疗慢性丙型肝炎的作用机制:研讨会纪要
Hepatology. 2008 Jan;47(1):306-20. doi: 10.1002/hep.22070.

免疫抑制作为眼表鳞状细胞癌中干扰素无反应的潜在危险因素。

Immunosuppression as a Possible Risk Factor for Interferon Nonresponse in Ocular Surface Squamous Neoplasia.

作者信息

Ashkenazy Noy, Karp Carol L, Wang Gaofeng, Acosta Carolina Mercado, Galor Anat

机构信息

*Department of Ophthalmology, Miami Veterans Affairs Medical Center; †Bascom Palmer Eye Institute, University of Miami, Miami, FL; and ‡Jackson Memorial Hospital, Miami, FL.

出版信息

Cornea. 2017 Apr;36(4):506-510. doi: 10.1097/ICO.0000000000001153.

DOI:10.1097/ICO.0000000000001153
PMID:28129301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5334142/
Abstract

PURPOSE

The mechanism by which ocular surface squamous neoplasia (OSSN) responds to topical interferon-alpha-2b (IFNα2b) is not known. We report the cases of 3 immunosuppressed patients whose tumors did not respond to topical IFNα2b therapy. The purpose of this series is to shed light on potential mechanisms of IFNα2b in OSSN.

METHODS

Retrospective case series of 3 immunosuppressed patients whose biopsy-proven OSSN did not respond to topical IFNα2b treatment.

RESULTS

Three white, immunosuppressed males (mean age 70 years, range 66-76) were diagnosed with OSSN. Topical IFNα2b 1 million units/mL was administered 4 times a day and used for a mean of 5 months (range 2-7 mo) without an adequate response. All patients were then switched to 5-fluorouracil. Successful eradication of OSSN was achieved in 2 cases, and improvement of OSSN in another. The latter patient was switched to mitomycin-C with subsequent resolution of OSSN.

CONCLUSIONS

These cases suggest that an intact immune system may be an important link between IFNα2b therapy and tumor resolution. As such, topical IFNα2b may not be an optimal choice for patients with underlying immunosuppression. It may be more effective in this patient population to switch to a non-immune-modulating therapy such as 5-fluorouracil or mitomycin-C.

摘要

目的

眼表鳞状上皮瘤变(OSSN)对局部应用干扰素-α-2b(IFNα2b)的反应机制尚不清楚。我们报告了3例免疫抑制患者的病例,他们的肿瘤对局部IFNα2b治疗无反应。本系列病例的目的是阐明IFNα2b在OSSN中的潜在作用机制。

方法

对3例经活检证实的OSSN且对局部IFNα2b治疗无反应的免疫抑制患者进行回顾性病例系列研究。

结果

3例白人免疫抑制男性(平均年龄70岁,范围66 - 76岁)被诊断为OSSN。局部应用100万单位/毫升的IFNα2b,每天4次,平均使用5个月(范围2 - 7个月),但未获得充分反应。所有患者随后改用5-氟尿嘧啶。2例患者成功根除OSSN,另1例患者病情有所改善。后1例患者改用丝裂霉素-C,随后OSSN得到缓解。

结论

这些病例表明,完整的免疫系统可能是IFNα2b治疗与肿瘤消退之间的重要联系。因此,对于存在潜在免疫抑制的患者,局部应用IFNα2b可能不是最佳选择。对于这类患者,改用如5-氟尿嘧啶或丝裂霉素-C等非免疫调节疗法可能更有效。