4.6 Review

Approaches to Enhance Natural Killer Cell-Based Immunotherapy for Pediatric Solid Tumors

期刊

CANCERS
卷 13, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13112796

关键词

NK cells; childhood cancer; solid tumor; neuroblastoma; Ewing sarcoma; rhabdomyosarcoma; osteosarcoma; hepatoblastoma; chimeric antigen receptor; CAR NK cells

类别

资金

  1. Bridge to the Doctorate Fellowship
  2. SciMed GRS Fellowship
  3. National Science Foundation Graduate Research Fellowship Program [DGE-1747503]
  4. Ruth M. Vetter Fellowship in Pediatric Hematology, Oncology, and Bone Marrow Transplant
  5. NIGMS/NIH [T32 GM008692]
  6. NCI/NIH [R01 CA215461, T32 CA009135]
  7. St. Baldrick's-Stand up to Cancer Pediatric Dream Team Translational Research Grant [SU2C-AACRDT-27-17]
  8. American Cancer Society [RSG-18-104-01LIB]
  9. MACC Fund
  10. American Association for Cancer Research, the Scientific Partner of SU2C

向作者/读者索取更多资源

Children with metastatic solid tumors have poor prognosis, but altering NK cells in the immune system may hold promise for recognizing and eliminating cancer. However, challenges remain in effectively using NK cells for treatment.
Simple Summary Children with metastatic solid tumors typically have a very poor prognosis, especially when the cancer returns or is resistant to upfront treatment. There is hope that the cells in the immune system can be programmed to help patients recognize and eliminate their cancer. Natural killer (NK) cells are an important component of the immune system designed to eliminate virally infected cells and tumors. In the last 20 years, advances in cell manufacturing have allowed investigators to grow NK cells in the laboratory to high numbers and engineer the cells to become highly potent. While some clinical trials using NK cells in children with solid tumors have shown promise, we still have much to learn on how to use NK cells effectively. This review will discuss our current understanding of NK cell biology and its relevance to solid tumors that commonly affect children. Treatment of metastatic pediatric solid tumors remain a significant challenge, particularly in relapsed and refractory settings. Standard treatment has included surgical resection, radiation, chemotherapy, and, in the case of neuroblastoma, immunotherapy. Despite such intensive therapy, cancer recurrence is common, and most tumors become refractory to prior therapy, leaving patients with few conventional treatment options. Natural killer (NK) cells are non-major histocompatibility complex (MHC)-restricted lymphocytes that boast several complex killing mechanisms but at an added advantage of not causing graft-versus-host disease, making use of allogeneic NK cells a potential therapeutic option. On top of their killing capacity, NK cells also produce several cytokines and growth factors that act as key regulators of the adaptive immune system, positioning themselves as ideal effector cells for stimulating heavily pretreated immune systems. Despite this promise, clinical efficacy of adoptive NK cell therapy to date has been inconsistent, prompting a detailed understanding of the biological pathways within NK cells that can be leveraged to develop next generation NK cell therapies. Here, we review advances in current approaches to optimizing the NK cell antitumor response including combination with other immunotherapies, cytokines, checkpoint inhibition, and engineering NK cells with chimeric antigen receptors (CARs) for the treatment of pediatric solid tumors.

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