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1
Photodynamic therapy with recombinant adenovirus AdmIL-12 enhances anti-tumour therapy efficacy in human papillomavirus 16 (E6/E7) infected tumour model.重组腺病毒AdmIL-12介导的光动力疗法增强了人乳头瘤病毒16(E6/E7)感染肿瘤模型中的抗肿瘤治疗效果。
Immunology. 2008 Aug;124(4):461-8. doi: 10.1111/j.1365-2567.2007.02797.x. Epub 2008 Apr 4.
2
Photodynamic therapy-generated tumor cell lysates with CpG-oligodeoxynucleotide enhance immunotherapy efficacy in human papillomavirus 16 (E6/E7) immortalized tumor cells.光动力疗法产生的肿瘤细胞裂解物与CpG寡脱氧核苷酸可增强人乳头瘤病毒16(E6/E7)永生化肿瘤细胞的免疫治疗效果。
Cancer Sci. 2007 May;98(5):747-52. doi: 10.1111/j.1349-7006.2007.00447.x.
3
A therapy modality using recombinant IL-12 adenovirus plus E7 protein in a human papillomavirus 16 E6/E7-associated cervical cancer animal model.在人乳头瘤病毒16型E6/E7相关宫颈癌动物模型中使用重组白细胞介素-12腺病毒加E7蛋白的一种治疗方式。
Hum Gene Ther. 2003 Oct 10;14(15):1389-99. doi: 10.1089/104303403769211619.
4
Suppression of antitumour protective cytotoxic T lymphocyte responses to a human papillomavirus 16 E7 DNA vaccine by coinjection of interleukin-12 complementary DNA: involvement of nitric oxide in immune suppression.白细胞介素-12 cDNA 共注射抑制人乳头瘤病毒 16 E7 DNA 疫苗诱导的抗肿瘤保护性细胞毒性 T 淋巴细胞反应:一氧化氮在免疫抑制中的作用。
Immunology. 2009 Sep;128(1 Suppl):e707-17. doi: 10.1111/j.1365-2567.2009.03068.x. Epub 2009 Feb 9.
5
Macrophages transduced with an adenoviral vector expressing interleukin 12 suppress tumor growth and metastasis in a preclinical metastatic prostate cancer model.用表达白细胞介素12的腺病毒载体转导的巨噬细胞在临床前转移性前列腺癌模型中抑制肿瘤生长和转移。
Cancer Res. 2003 Nov 15;63(22):7853-60.
6
Immunization with adenoviral vectors carrying recombinant IL-12 and E7 enhanced the antitumor immunity to human papillomavirus 16-associated tumor.用携带重组白细胞介素-12和E7的腺病毒载体进行免疫接种可增强对人乳头瘤病毒16相关肿瘤的抗肿瘤免疫力。
Gynecol Oncol. 2005 May;97(2):559-67. doi: 10.1016/j.ygyno.2005.01.046.
7
Coadministration of the fungal immunomodulatory protein FIP-Fve and a tumour-associated antigen enhanced antitumour immunity.真菌免疫调节蛋白 FIP-Fve 与肿瘤相关抗原联合应用增强了抗肿瘤免疫。
Immunology. 2009 Sep;128(1 Suppl):e881-94. doi: 10.1111/j.1365-2567.2009.03099.x. Epub 2009 Mar 26.
8
Cooperative effects of adenoviral vector-mediated interleukin 12 gene therapy with radiotherapy in a preclinical model of metastatic prostate cancer.腺病毒载体介导的白细胞介素12基因治疗与放疗在转移性前列腺癌临床前模型中的协同作用。
Gene Ther. 2007 Feb;14(3):227-36. doi: 10.1038/sj.gt.3302788. Epub 2006 Oct 5.
9
Prostate cancer gene therapy: comparison of adenovirus-mediated expression of interleukin 12 with interleukin 12 plus B7-1 for in situ gene therapy and gene-modified, cell-based vaccines.前列腺癌基因治疗:腺病毒介导的白细胞介素12表达与白细胞介素12加B7-1用于原位基因治疗和基因修饰的细胞疫苗的比较。
Clin Cancer Res. 2000 Oct;6(10):4101-9.
10
Interleukin-2 gene transfer potentiates the alpha-galactosylceramide-stimulated antitumor effect by the induction of TRAIL in NKT and NK cells in mouse models of subcutaneous and metastatic carcinoma.白细胞介素-2 基因转移通过诱导 TRAIL 在 NKT 和 NK 细胞中增强 α-半乳糖神经酰胺刺激的抗肿瘤作用,在皮下和转移性癌的小鼠模型中。
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2
Targeting immunogenic cancer cell death by photodynamic therapy: past, present and future.通过光动力疗法靶向免疫原性癌细胞死亡:过去、现在和未来。
J Immunother Cancer. 2021 Jan;9(1). doi: 10.1136/jitc-2020-001926.
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Photodynamic therapy for gynecological diseases and breast cancer.光动力学疗法在妇科疾病和乳腺癌中的应用。
Cancer Biol Med. 2012 Mar;9(1):9-17. doi: 10.3969/j.issn.2095-3941.2012.01.002.
5
Therapeutic effects of systemic photodynamic therapy in a leukemia animal model using A20 cells.A20 细胞用于白血病动物模型的全身光动力疗法的治疗效果。
Lasers Med Sci. 2012 Mar;27(2):445-52. doi: 10.1007/s10103-011-0950-x. Epub 2011 Jul 18.
6
Photodynamic therapy of cancer: an update.光动力疗法治疗癌症:最新进展。
CA Cancer J Clin. 2011 Jul-Aug;61(4):250-81. doi: 10.3322/caac.20114. Epub 2011 May 26.

本文引用的文献

1
Photodynamic therapy-generated tumor cell lysates with CpG-oligodeoxynucleotide enhance immunotherapy efficacy in human papillomavirus 16 (E6/E7) immortalized tumor cells.光动力疗法产生的肿瘤细胞裂解物与CpG寡脱氧核苷酸可增强人乳头瘤病毒16(E6/E7)永生化肿瘤细胞的免疫治疗效果。
Cancer Sci. 2007 May;98(5):747-52. doi: 10.1111/j.1349-7006.2007.00447.x.
2
C225 and PDT combination therapy for ovarian cancer: the play's the thing.西妥昔单抗(C225)与光动力疗法(PDT)联合治疗卵巢癌:关键在于行动。
J Natl Cancer Inst. 2005 Oct 19;97(20):1488-9. doi: 10.1093/jnci/dji360.
3
Celecoxib and NS-398 enhance photodynamic therapy by increasing in vitro apoptosis and decreasing in vivo inflammatory and angiogenic factors.塞来昔布和NS-398通过增加体外细胞凋亡以及减少体内炎症和血管生成因子来增强光动力疗法。
Cancer Res. 2005 Oct 15;65(20):9473-8. doi: 10.1158/0008-5472.CAN-05-1659.
4
Immunization with adenoviral vectors carrying recombinant IL-12 and E7 enhanced the antitumor immunity to human papillomavirus 16-associated tumor.用携带重组白细胞介素-12和E7的腺病毒载体进行免疫接种可增强对人乳头瘤病毒16相关肿瘤的抗肿瘤免疫力。
Gynecol Oncol. 2005 May;97(2):559-67. doi: 10.1016/j.ygyno.2005.01.046.
5
The present and future role of photodynamic therapy in cancer treatment.光动力疗法在癌症治疗中的当前及未来作用。
Lancet Oncol. 2004 Aug;5(8):497-508. doi: 10.1016/S1470-2045(04)01529-3.
6
Interleukin-12 inhibits tumor growth in a novel angiogenesis canine hemangiosarcoma xenograft model.白细胞介素-12在一种新型血管生成犬血管肉瘤异种移植模型中抑制肿瘤生长。
Neoplasia. 2004 Mar-Apr;6(2):106-16. doi: 10.1593/neo.03334.
7
Photodynamic effect of novel chlorin e6 derivatives on a single nerve cell.新型二氢卟吩e6衍生物对单个神经细胞的光动力效应。
Life Sci. 2004 Mar 12;74(17):2185-97. doi: 10.1016/j.lfs.2003.09.053.
8
A therapy modality using recombinant IL-12 adenovirus plus E7 protein in a human papillomavirus 16 E6/E7-associated cervical cancer animal model.在人乳头瘤病毒16型E6/E7相关宫颈癌动物模型中使用重组白细胞介素-12腺病毒加E7蛋白的一种治疗方式。
Hum Gene Ther. 2003 Oct 10;14(15):1389-99. doi: 10.1089/104303403769211619.
9
Contribution of CD8(+) T cells to gamma interferon production in human tuberculosis.CD8(+) T细胞在人类结核病中对γ干扰素产生的作用。
Infect Immun. 2001 May;69(5):3497-501. doi: 10.1128/IAI.69.5.3497-3501.2001.
10
Immunological and viral factors associated with the response of vulval intraepithelial neoplasia to photodynamic therapy.与外阴上皮内瘤变对光动力疗法反应相关的免疫和病毒因素。
Cancer Res. 2001 Jan 1;61(1):192-6.

重组腺病毒AdmIL-12介导的光动力疗法增强了人乳头瘤病毒16(E6/E7)感染肿瘤模型中的抗肿瘤治疗效果。

Photodynamic therapy with recombinant adenovirus AdmIL-12 enhances anti-tumour therapy efficacy in human papillomavirus 16 (E6/E7) infected tumour model.

作者信息

Park Eun Kyung, Bae Su-Mi, Kwak Sun-Young, Lee Sung Jong, Kim Yong-Wook, Han Chan-Hee, Cho Hyun-Jung, Kim Kyung Tae, Kim Young-Jae, Kim Hyun-Jung, Ahn Woong Shick

机构信息

Department of Obstetrics and Gynecology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Immunology. 2008 Aug;124(4):461-8. doi: 10.1111/j.1365-2567.2007.02797.x. Epub 2008 Apr 4.

DOI:10.1111/j.1365-2567.2007.02797.x
PMID:18397271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2492938/
Abstract

Immunotherapy with photodynamic therapy (PDT) offers great promise as a new alternative for cancer treatment; however, its use remains experimental. Here we investigated the utility of adenoviral delivery of interleukin-12 (AdmIL-12) as an adjuvant for PDT in mouse tumour challenge model. PDT was performed by irradiating Radachlorin in C57BL/6 mice transplanted with TC-1 cells. PDT plus AdmIL-12 treatment for tumour suppression as well as specific immune responses were evaluated with the following tests: in vitro and in vivo tumour growth inhibition, interferon-gamma (IFN-gamma) and tumour necrosis factor-alpha (TNF-alpha) assay, and cytotoxic T lymphocyte (CTL) assay. Direct intratumoral injection of AdmIL-12 resulted in a significant suppression of tumour growth compared to the control group. Treatment of PDT along with AdmIL-12 further enhanced antitumour effects significantly higher than either AdmIL-12 or PDT alone. This combined treatment resulted in complete regression of 9-mm sized tumour in every animal. We also evaluated immune responses induced by these treatments. Combined treatment significantly increased the production level of IFN-gamma and TNF-alpha compared with that by AdmIL-12 or PDT alone. PDT plus AdmIL-12 enhanced antitumour immunity through increased expansion of the CTL subset mediated by CD8+ T cells. Taken together, these results indicate that the high anti-cancer activity of PDT with AdmIL-12 is a powerful tool against cancer therapy and is a promising subject for further investigation.

摘要

光动力疗法(PDT)免疫疗法作为一种癌症治疗的新选择具有很大的前景;然而,其应用仍处于实验阶段。在这里,我们在小鼠肿瘤攻击模型中研究了腺病毒介导的白细胞介素-12(AdmIL-12)作为PDT佐剂的效用。通过照射移植了TC-1细胞的C57BL/6小鼠体内的拉达氯林来进行PDT。通过以下测试评估PDT加AdmIL-12治疗对肿瘤抑制以及特异性免疫反应的效果:体外和体内肿瘤生长抑制、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)测定以及细胞毒性T淋巴细胞(CTL)测定。与对照组相比,直接瘤内注射AdmIL-12导致肿瘤生长显著受到抑制。PDT与AdmIL-12联合治疗进一步显著增强了抗肿瘤效果,明显高于单独使用AdmIL-12或PDT。这种联合治疗使每只动物体内9毫米大小的肿瘤完全消退。我们还评估了这些治疗诱导的免疫反应。与单独使用AdmIL-12或PDT相比,联合治疗显著提高了IFN-γ和TNF-α的产生水平。PDT加AdmIL-12通过增加由CD8 + T细胞介导的CTL亚群的扩增来增强抗肿瘤免疫力。综上所述,这些结果表明,PDT与AdmIL-12的高抗癌活性是对抗癌症治疗的有力工具,并且是进一步研究的有希望的课题。