Immunotherapy for neuroblastoma by hematopoietic cell transplantation and post-transplant immunomodulation

被引:2
作者
Ash, Shifra [1 ,2 ]
Askenasy, Nadir [2 ]
机构
[1] Technion Israel Inst Technol, Ruth Rappaport Childrens Hosp, Pediat Hematol Oncol & Bone Marrow Transplantat D, Rambam Hlth Care Campus, Haifa, Israel
[2] Schneider Childrens Med Ctr Israel, Frankel Lab Bone Marrow Transplantat, Petah Tiqwa, Israel
关键词
Neuroblastoma; Hematopoietic cell transplantation; Lymphocyte infusion; Antigen-presenting cells; Graft versus tumor; Graft versus host disease; BONE-MARROW-TRANSPLANTATION; GRAFT-VERSUS-LEUKEMIA; HIGH-RISK NEUROBLASTOMA; DONOR LYMPHOCYTE INFUSION; ANTIGEN-PRESENTING CELLS; PULSED DENDRITIC CELLS; NATURAL-KILLER-CELLS; REACTIVE T-CELLS; MINOR HISTOCOMPATIBILITY ANTIGENS; TUMOR GANGLIOSIDES INHIBIT;
D O I
10.1016/j.critrevonc.2023.103956
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neuroblastoma represents a relatively common childhood tumor that imposes therapeutic difficulties. High risk neuroblastoma patients have poor prognosis, display limited response to radiochemotherapy and may be treated by hematopoietic cell transplantation. Allogeneic and haploidentical transplants have the distinct advantage of reinstitution of immune surveillance, reinforced by antigenic barriers. The key factors favorable to ignition of potent anti-tumor reactions are transition to adaptive immunity, recovery from lymphopenia and removal of inhibitory signals that inactivate immune cells at the local and systemic levels. Post-transplant immunomodulation may further foster anti-tumor reactivity, with positive but transient impact of infusions of lymphocytes and natural killer cells both from the donor, the recipient or third party. The most promising approaches include introduction of antigen-presenting cells in early post-transplant stages and neutralization of inhibitory signals. Further studies will likely shed light on the nature and actions of suppressor factors within tumor stroma and at the systemic level.
引用
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页数:12
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