• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

转移性恶性黑色素瘤中的肿瘤浸润淋巴细胞及对α干扰素治疗的反应

Tumour-infiltrating lymphocytes in metastatic malignant melanoma and response to interferon alpha treatment.

作者信息

Håkansson A, Gustafsson B, Krysander L, Håkansson L

机构信息

Department of Oncology, University Hospital, Linköping, Sweden.

出版信息

Br J Cancer. 1996 Sep;74(5):670-6. doi: 10.1038/bjc.1996.420.

DOI:10.1038/bjc.1996.420
PMID:8845294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2074699/
Abstract

Interferon alpha (IFN-alpha) has a documented activity against malignant melanoma with a response rate of only approximately 20%. It would therefore be of considerable importance if patients likely to respond could be identified. The degree of mononuclear cell infiltration in primary tumours has been reported to correlate with a favourable prognosis. This investigation used monoclonal antibodies, anti-CD4, -CD8 and -CD11c, to identify subsets of tumour-infiltrating mononuclear cells in fine needle aspirates to study whether the presence of such cells correlates with the therapeutic effect of IFN-alpha. Twenty-one patients with systemic and 20 with regional metastatic malignant melanoma were studied before initiation of IFN-alpha treatment. A statistically significant correlation (P < 0.001) was found between the occurrence of CD4+ lymphocytes in fine needle aspirates and the therapeutic benefit of IFN-alpha in patients with systemic disease. Ten out of 11 with moderate to high numbers of infiltrating CD4+ lymphocytes achieved tumour regression. In contrast, among patients with low numbers of these cells in metastatic lesions, nine out of ten had progressive disease. Similar results were found in patients with regional disease.

摘要

α干扰素(IFN-α)对恶性黑色素瘤具有已被证实的活性,但其缓解率仅约为20%。因此,如果能够识别出可能有反应的患者,将具有相当重要的意义。据报道,原发性肿瘤中单核细胞浸润程度与预后良好相关。本研究使用抗CD4、抗CD8和抗CD11c单克隆抗体,在细针穿刺抽吸物中识别肿瘤浸润单核细胞亚群,以研究这些细胞的存在是否与IFN-α的治疗效果相关。在开始IFN-α治疗前,对21例全身性和20例区域性转移性恶性黑色素瘤患者进行了研究。在细针穿刺抽吸物中CD4+淋巴细胞的出现与全身性疾病患者IFN-α的治疗益处之间发现了具有统计学意义的相关性(P < 0.001)。11例有中度至高数量浸润性CD4+淋巴细胞的患者中有10例实现了肿瘤消退。相比之下,在转移病灶中这些细胞数量较少的患者中,10例中有9例病情进展。在区域性疾病患者中也发现了类似结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/f084864b6148/brjcancer00021-0012-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/32766571dfb0/brjcancer00021-0010-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/dd68ce682597/brjcancer00021-0011-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/f084864b6148/brjcancer00021-0012-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/32766571dfb0/brjcancer00021-0010-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/dd68ce682597/brjcancer00021-0011-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c7/2074699/f084864b6148/brjcancer00021-0012-a.jpg

相似文献

1
Tumour-infiltrating lymphocytes in metastatic malignant melanoma and response to interferon alpha treatment.转移性恶性黑色素瘤中的肿瘤浸润淋巴细胞及对α干扰素治疗的反应
Br J Cancer. 1996 Sep;74(5):670-6. doi: 10.1038/bjc.1996.420.
2
Biochemotherapy of metastatic malignant melanoma. Predictive value of tumour-infiltrating lymphocytes.转移性恶性黑色素瘤的生物化疗。肿瘤浸润淋巴细胞的预测价值。
Br J Cancer. 2001 Dec 14;85(12):1871-7. doi: 10.1054/bjoc.2001.2169.
3
Effect of IFN-alpha on tumor-infiltrating mononuclear cells and regressive changes in metastatic malignant melanoma.干扰素-α对肿瘤浸润单核细胞的作用及转移性恶性黑色素瘤的退行性变化
J Interferon Cytokine Res. 1998 Jan;18(1):33-9. doi: 10.1089/jir.1998.18.33.
4
Expression of ICAM-1 during IFN-alpha-based treatment of metastatic malignant melanoma: relation to tumor-infiltrating mononuclear cells and regressive tumor changes.基于干扰素-α治疗转移性恶性黑色素瘤期间细胞间黏附分子-1的表达:与肿瘤浸润单核细胞及肿瘤消退变化的关系
J Interferon Cytokine Res. 1999 Feb;19(2):171-7. doi: 10.1089/107999099314315.
5
Clinical responses and lymphoid infiltrates in metastatic melanoma following treatment with intralesional GM-CSF.病灶内注射粒细胞-巨噬细胞集落刺激因子(GM-CSF)治疗转移性黑色素瘤后的临床反应及淋巴细胞浸润情况
Melanoma Res. 1996 Jun;6(3):247-55. doi: 10.1097/00008390-199606000-00008.
6
Infiltration of mononuclear inflammatory cells into primary colorectal carcinomas: an immunohistological analysis.原发性结直肠癌中单核炎性细胞浸润:一项免疫组织学分析。
Br J Cancer. 1997;75(3):374-80. doi: 10.1038/bjc.1997.61.
7
Tumor-infiltrating lymphocytes in patients with metastatic melanoma receiving chemoimmunotherapy.接受化学免疫疗法的转移性黑色素瘤患者的肿瘤浸润淋巴细胞
J Immunother. 1997 Nov;20(6):488-95. doi: 10.1097/00002371-199711000-00009.
8
Inflammatory cell infiltrates in advanced metastatic uveal melanoma.晚期转移性葡萄膜黑色素瘤中的炎性细胞浸润。
Hum Pathol. 2017 Aug;66:159-166. doi: 10.1016/j.humpath.2017.06.005. Epub 2017 Jun 24.
9
Tumour-associated macrophages are related to progression in patients with metastatic melanoma following interleukin-2 based immunotherapy.肿瘤相关巨噬细胞与接受白细胞介素-2免疫治疗的转移性黑色素瘤患者的病情进展有关。
Acta Oncol. 2006;45(4):400-5. doi: 10.1080/02841860500471798.
10
Characterization of proliferative cells in malignant melanomas and their inflammatory infiltrates.恶性黑色素瘤中增殖细胞及其炎性浸润的特征分析
Cancer Detect Prev. 1991;15(3):183-7.

引用本文的文献

1
Improved prognosis and evidence of enhanced immunogenicity in tumor and circulation of high-risk melanoma patients with unknown primary.对于原发灶不明的高危黑色素瘤患者,肿瘤和循环中存在更好的预后和增强免疫原性的证据。
J Immunother Cancer. 2022 Jan;10(1). doi: 10.1136/jitc-2021-004310.
2
CTLA-4 blockade and interferon-α induce proinflammatory transcriptional changes in the tumor immune landscape that correlate with pathologic response in melanoma.CTLA-4 阻断和干扰素-α 在肿瘤免疫图谱中诱导促炎转录变化,与黑色素瘤的病理反应相关。
PLoS One. 2021 Jan 11;16(1):e0245287. doi: 10.1371/journal.pone.0245287. eCollection 2021.
3

本文引用的文献

1
Interferon alfa-2b adjuvant therapy of high-risk resected cutaneous melanoma: the Eastern Cooperative Oncology Group Trial EST 1684.高危切除性皮肤黑色素瘤的干扰素α-2b辅助治疗:东部肿瘤协作组试验EST 1684
J Clin Oncol. 1996 Jan;14(1):7-17. doi: 10.1200/JCO.1996.14.1.7.
2
Histologic regression in malignant melanoma: an interobserver concordance study.恶性黑色素瘤的组织学消退:一项观察者间一致性研究。
J Cutan Pathol. 1993 Apr;20(2):126-9. doi: 10.1111/j.1600-0560.1993.tb00228.x.
3
Differential immune reactivity of tumour-intrinsic and peripheral-blood lymphocytes against autoplastic colorectal carcinoma cells.
Downregulation of RIG-I mediated by ITGB3/c-SRC/STAT3 signaling confers resistance to interferon-α-induced apoptosis in tumor-repopulating cells of melanoma.
ITGB3/c-SRC/STAT3 信号下调 RIG-I 介导的干扰素-α诱导的黑色素瘤肿瘤再生细胞凋亡抵抗。
J Immunother Cancer. 2020 Mar;8(1). doi: 10.1136/jitc-2019-000111.
4
Immunotherapy in Pediatric Solid Tumors-A Systematic Review.儿童实体瘤的免疫治疗——一项系统综述
Cancers (Basel). 2019 Dec 14;11(12):2022. doi: 10.3390/cancers11122022.
5
Neoadjuvant therapy of locally/regionally advanced melanoma.局部/区域晚期黑色素瘤的新辅助治疗
Ther Adv Med Oncol. 2019 Jul 31;11:1758835919866959. doi: 10.1177/1758835919866959. eCollection 2019.
6
Tanapoxvirus lacking the 15L gene inhibits melanoma cell growth in vitro by inducing interferon-λ1 release.缺失15L基因的塔纳痘病毒通过诱导干扰素-λ1释放来抑制黑色素瘤细胞的体外生长。
Virus Genes. 2017 Jun;53(3):477-482. doi: 10.1007/s11262-017-1434-2. Epub 2017 Feb 10.
7
Phase II trial of pegylated interferon alfa-2b in young patients with neurofibromatosis type 1 and unresectable plexiform neurofibromas.聚乙二醇化干扰素α-2b治疗1型神经纤维瘤病年轻患者及不可切除丛状神经纤维瘤的II期试验。
Neuro Oncol. 2017 Feb 1;19(2):289-297. doi: 10.1093/neuonc/now158.
8
Pro-Inflammatory Cytokines Predict Relapse-Free Survival after One Month of Interferon-α but Not Observation in Intermediate Risk Melanoma Patients.促炎细胞因子可预测中度风险黑色素瘤患者接受α干扰素治疗1个月后的无复发生存率,但对观察等待患者无此预测作用。
PLoS One. 2015 Jul 20;10(7):e0132745. doi: 10.1371/journal.pone.0132745. eCollection 2015.
9
Recent advances in the development of breast cancer vaccines.乳腺癌疫苗研发的最新进展。
Breast Cancer (Dove Med Press). 2014 Oct 14;6:159-68. doi: 10.2147/BCTT.S38428. eCollection 2014.
10
Type I interferons: key players in normal skin and select cutaneous malignancies.I型干扰素:正常皮肤和特定皮肤恶性肿瘤中的关键角色。
Dermatol Res Pract. 2014;2014:847545. doi: 10.1155/2014/847545. Epub 2014 Jan 5.
肿瘤内在淋巴细胞和外周血淋巴细胞对自身结肠癌细胞的差异性免疫反应性。
Br J Cancer. 1981 Sep;44(3):396-402. doi: 10.1038/bjc.1981.197.
4
Prolonged survival for melanoma patients with elevated IgM antibody to oncofetal antigen.癌胚抗原IgM抗体升高的黑色素瘤患者生存期延长。
J Natl Cancer Inst. 1981 Feb;66(2):249-54.
5
Immunoperoxidase localization of lymphocyte subsets in the host response to melanoma and nevi.黑色素瘤和痣宿主反应中淋巴细胞亚群的免疫过氧化物酶定位
Cancer Res. 1983 Jun;43(6):2749-53.
6
In situ analysis of the mononuclear cell infiltrate in primary malignant melanoma of the skin.皮肤原发性恶性黑色素瘤中单核细胞浸润的原位分析。
Clin Exp Immunol. 1983 Jan;51(1):77-82.
7
Major histocompatibility antigens and mononuclear inflammatory infiltrate in benign nevomelanocytic proliferations and malignant melanoma.良性痣细胞增生和恶性黑色素瘤中的主要组织相容性抗原与单核炎性浸润
J Immunol. 1982 Dec;129(6):2808-15.
8
Tumor thickness and lymphocytic infiltration in malignant melanoma of the head and neck.头颈部恶性黑色素瘤的肿瘤厚度及淋巴细胞浸润情况
Am J Surg. 1974 Oct;128(4):557-61. doi: 10.1016/0002-9610(74)90275-x.
9
Partial regression in thin primary cutaneous malignant melanomas clinical stage I. A study of 486 cases.I期临床的原发性皮肤薄恶性黑色素瘤的部分回归。486例研究。
Virchows Arch A Pathol Anat Histopathol. 1985;408(2-3):241-7. doi: 10.1007/BF00707986.
10
Thin malignant melanomas with regression and metastases.伴有消退和转移的薄型恶性黑色素瘤。
Arch Dermatol. 1987 Oct;123(10):1326-30.