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SENTI-101, a Preparation of Mesenchymal Stromal Cells Engineered to Express IL12 and IL21, Induces Localized and Durable Antitumor Immunity in Preclinical Models of Peritoneal Solid Tumors.
Gonzalez-Junca, Alba; Liu, Frances D; Nagaraja, Archana S; Mullenix, Alyssa; Lee, Chen-Ting; Gordley, Russell M; Frimannsson, Daniel O; Maller, Ori; Garrison, Brian S; Iyer, Dharini; Benabbas, Anissa; Truong, Tiffany A; Quach, Allison; Tian, Mengxi; Martinez, Rowena; Savur, Rishi; Perry-McNamara, Alyssa; Nguyen, Denny; Almudhfar, Niran; Blanco, Carmina; Huynh, Christina; Nand, Asish; Lay, Yu-An E; Magal, Ashita; Mangalampalli, Sravani; Lee, Philip J; Lu, Timothy K; Lee, Gary.
Afiliação
  • Gonzalez-Junca A; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California. alba.gonzalez@sentibio.com.
  • Liu FD; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Nagaraja AS; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Mullenix A; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Lee CT; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Gordley RM; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Frimannsson DO; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Maller O; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Garrison BS; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Iyer D; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Benabbas A; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Truong TA; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Quach A; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Tian M; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Martinez R; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Savur R; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Perry-McNamara A; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Nguyen D; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Almudhfar N; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Blanco C; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
  • Huynh C; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Nand A; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Lay YE; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Magal A; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Mangalampalli S; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Lee PJ; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Lu TK; Department of Technology and Operations, Senti Biosciences, Inc., South San Francisco, California.
  • Lee G; Department of Research and Development, Senti Biosciences, Inc., South San Francisco, California.
Mol Cancer Ther ; 20(9): 1508-1520, 2021 09.
Article em En | MEDLINE | ID: mdl-34210826
ABSTRACT
Advanced peritoneal carcinomatosis including high-grade ovarian cancer has poor prognoses and a poor response rate to current checkpoint inhibitor immunotherapies; thus, there is an unmet need for effective therapeutics that would provide benefit to these patients. Here we present the preclinical development of SENTI-101, a cell preparation of bone marrow-derived mesenchymal stromal (also known as stem) cells (MSC), which are engineered to express two potent immune-modulatory cytokines, IL12 and IL21. Intraperitoneal administration of SENTI-101 results in selective tumor-homing and localized and sustained cytokine production in murine models of peritoneal cancer. SENTI-101 has extended half-life, reduced systemic distribution, and improved antitumor activity when compared with recombinant cytokines, suggesting that it is more effective and has lower risk of systemic immunotoxicities. Treatment of tumor-bearing immune-competent mice with a murine surrogate of SENTI-101 (mSENTI-101) results in a potent and localized immune response consistent with increased number and activation of antigen presenting cells, T cells and B cells, which leads to antitumor response and memory-induced long-term immunity. Consistent with this mechanism of action, co-administration of mSENTI-101 with checkpoint inhibitors leads to synergistic improvement in antitumor response. Collectively, these data warrant potential clinical development of SENTI-101 for patients with peritoneal carcinomatosis and high-grade ovarian cancer.Graphical abstract SENTI-101 schematic and mechanism of actionSENTI-101 is a novel cell-based immunotherapeutic consisting of bone marrow-derived mesenchymal stromal cells (BM-MSC) engineered to express IL12 and IL21 intended for the treatment of peritoneal carcinomatosis including high-grade serous ovarian cancer. Upon intraperitoneal administration, SENTI-101 homes to peritoneal solid tumors and secretes IL12 and IL21 in a localized and sustained fashion. The expression of these two potent cytokines drives tumor infiltration and engagement of multiple components of the immune system antigen-presenting cells, T cells, and B cells, resulting in durable antitumor immunity in preclinical models of cancer.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Peritoneais / Melanoma Experimental / Interleucinas / Interleucina-12 / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Peritoneais / Melanoma Experimental / Interleucinas / Interleucina-12 / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article