دورية أكاديمية

Neutrophil-activating therapy for the treatment of cancer.

التفاصيل البيبلوغرافية
العنوان: Neutrophil-activating therapy for the treatment of cancer.
المؤلفون: Linde IL; Program in Immunology, Stanford University, Stanford, CA 94305, USA; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Prestwood TR; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Qiu J; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Pilarowski G; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Linde MH; Program in Immunology, Stanford University, Stanford, CA 94305, USA., Zhang X; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Shen L; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Reticker-Flynn NE; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Chiu DK; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Sheu LY; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Van Deursen S; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Tolentino LL; Department of Pathology, Stanford University, Stanford, CA 94305, USA., Song WC; Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Engleman EG; Program in Immunology, Stanford University, Stanford, CA 94305, USA; Department of Pathology, Stanford University, Stanford, CA 94305, USA. Electronic address: edengleman@stanford.edu.
المصدر: Cancer cell [Cancer Cell] 2023 Feb 13; Vol. 41 (2), pp. 356-372.e10. Date of Electronic Publication: 2023 Jan 26.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 101130617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-3686 (Electronic) Linking ISSN: 15356108 NLM ISO Abbreviation: Cancer Cell Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Cambridge, Mass. : Cell Press, c2002-
مواضيع طبية MeSH: Neoplasms*/drug therapy , Neoplasms*/metabolism , Antineoplastic Agents*, Mice ; Animals ; Humans ; Neutrophils ; Leukotriene B4/metabolism ; Leukotriene B4/pharmacology ; Tumor Necrosis Factor-alpha/metabolism
مستخلص: Despite their cytotoxic capacity, neutrophils are often co-opted by cancers to promote immunosuppression, tumor growth, and metastasis. Consequently, these cells have received little attention as potential cancer immunotherapeutic agents. Here, we demonstrate in mouse models that neutrophils can be harnessed to induce eradication of tumors and reduce metastatic seeding through the combined actions of tumor necrosis factor, CD40 agonist, and tumor-binding antibody. The same combination activates human neutrophils in vitro, enabling their lysis of human tumor cells. Mechanistically, this therapy induces rapid mobilization and tumor infiltration of neutrophils along with complement activation in tumors. Complement component C5a activates neutrophils to produce leukotriene B 4 , which stimulates reactive oxygen species production via xanthine oxidase, resulting in oxidative damage and T cell-independent clearance of multiple tumor types. These data establish neutrophils as potent anti-tumor immune mediators and define an inflammatory pathway that can be harnessed to drive neutrophil-mediated eradication of cancer.
Competing Interests: Declaration of interests I.L.L., T.R.P., and E.G.E. are co-inventors on a patent application filed by Stanford University related to this work. W.-C.S. owns equity in, receives a consultant fee and research grant from, and is an inventor of patents licensed to Kira Pharmaceuticals and Aevitas Therapeutics. The other authors declare no competing interests.
(Copyright © 2023 Elsevier Inc. All rights reserved.)
التعليقات: Comment in: Cancer Cell. 2023 Feb 13;41(2):227-229. (PMID: 36787693)
Comment in: Nat Rev Cancer. 2023 Apr;23(4):190. (PMID: 36864183)
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معلومات مُعتمدة: R01 AI117410 United States AI NIAID NIH HHS; F31 CA196029 United States CA NCI NIH HHS; R01 CA233958 United States CA NCI NIH HHS; R01 AI146162 United States AI NIAID NIH HHS; R01 AI085596 United States AI NIAID NIH HHS; U54 CA209971 United States CA NCI NIH HHS; R01 CA262361 United States CA NCI NIH HHS; F32 CA189408 United States CA NCI NIH HHS; R01 CA222969 United States CA NCI NIH HHS; T32 HL120824 United States HL NHLBI NIH HHS; R01 CA251174 United States CA NCI NIH HHS; P01 CA244114 United States CA NCI NIH HHS; F30 CA196145 United States CA NCI NIH HHS
فهرسة مساهمة: Keywords: C5a; CD40; cancer immunotherapy; complement; leukotriene B4; neutrophil; reactive oxygen species; tumor immunology; tumor necrosis factor; xanthine oxidase
المشرفين على المادة: 0 (Antineoplastic Agents)
1HGW4DR56D (Leukotriene B4)
0 (Tumor Necrosis Factor-alpha)
تواريخ الأحداث: Date Created: 20230127 Date Completed: 20230216 Latest Revision: 20240214
رمز التحديث: 20240214
مُعرف محوري في PubMed: PMC9968410
DOI: 10.1016/j.ccell.2023.01.002
PMID: 36706760
قاعدة البيانات: MEDLINE
الوصف
تدمد:1878-3686
DOI:10.1016/j.ccell.2023.01.002