دورية أكاديمية

Umbilical cord blood CD34 + progenitor-derived NK cells efficiently kill ovarian cancer spheroids and intraperitoneal tumors in NOD/SCID/IL2Rg null mice.

التفاصيل البيبلوغرافية
العنوان: Umbilical cord blood CD34 + progenitor-derived NK cells efficiently kill ovarian cancer spheroids and intraperitoneal tumors in NOD/SCID/IL2Rg null mice.
المؤلفون: Hoogstad-van Evert JS; Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands.; Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands., Cany J; Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands., van den Brand D; Department of Biochemistry, Radboud University Medical Center, Nijmegen, the Netherlands., Oudenampsen M; Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands., Brock R; Department of Biochemistry, Radboud University Medical Center, Nijmegen, the Netherlands., Torensma R; Department of Tumor Immunology, Radboud University Medical Center, Nijmegen, the Netherlands., Bekkers RL; Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands., Jansen JH; Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands., Massuger LF; Department of Obstetrics and Gynecology, Radboud University Medical Center, Nijmegen, the Netherlands., Dolstra H; Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands.
المصدر: Oncoimmunology [Oncoimmunology] 2017 May 11; Vol. 6 (8), pp. e1320630. Date of Electronic Publication: 2017 May 11 (Print Publication: 2017).
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 101570526 Publication Model: eCollection Cited Medium: Print ISSN: 2162-4011 (Print) Linking ISSN: 21624011 NLM ISO Abbreviation: Oncoimmunology Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: 2015- : Philadelphia, PA : Taylor & Francis
Original Publication: Austin, TX : Landes Bioscience
مستخلص: Adoptive transfer of allogeneic natural killer (NK) cells is an attractive therapy approach against ovarian carcinoma. Here, we evaluated the potency of highly active NK cells derived from human CD34+ haematopoietic stem and progenitor cells (HSPC) to infiltrate and mediate killing of human ovarian cancer spheroids using an in vivo -like model system and mouse xenograft model. These CD56+Perforin+ HSPC-NK cells were generated under stroma-free conditions in the presence of StemRegenin-1, IL-15, and IL-12, and exerted efficient cytolytic activity and IFNγ production toward ovarian cancer monolayer cultures. Live-imaging confocal microscopy demonstrated that these HSPC-NK cells actively migrate, infiltrate, and mediate tumor cell killing in a three-dimensional multicellular ovarian cancer spheroid. Infiltration of up to 30% of total HSPC-NK cells within 8 h resulted in robust tumor spheroid destruction. Furthermore, intraperitoneal HSPC-NK cell infusions in NOD/SCID-IL2Rγ null (NSG) mice bearing ovarian carcinoma significantly reduced tumor progression. These findings demonstrate that highly functional HSPC-NK cells efficiently destruct ovarian carcinoma spheroids in vitro and kill intraperitoneal ovarian tumors in vivo , providing great promise for effective immunotherapy through intraperitoneal HSPC-NK cell adoptive transfer in ovarian carcinoma patients.
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فهرسة مساهمة: Keywords: Adoptive immunotherapy; NK cells; mouse ovarian cancer xenograft; ovarian cancer; tumor spheroid infiltration
تواريخ الأحداث: Date Created: 20170919 Latest Revision: 20210112
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC5593716
DOI: 10.1080/2162402X.2017.1320630
PMID: 28919991
قاعدة البيانات: MEDLINE
الوصف
تدمد:2162-4011
DOI:10.1080/2162402X.2017.1320630