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Cellular immunotherapy for hematological malignancy: recent progress and future perspectives

Journal

CANCER BIOLOGY & MEDICINE
Volume 18, Issue 4, Pages 966-980

Publisher

CHINA ANTI-CANCER ASSOC
DOI: 10.20892/j.issn.2095-3941.2020.0801

Keywords

Cellular immunotherapy; hematologic; CAR-T; NK; stem cell transplantation

Funding

  1. Foundation for Innovative Research Groups of the National Natural Science Foundation of China [81621001]
  2. Key Program of National Natural Science Foundation of China [81930004]
  3. National Key Research and Development Program of China [2017YFA0104500]

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Advancements in cellular immunotherapy have revolutionized the treatment of hematologic malignancies by utilizing the patient's immune system to target cancer cells. While CAR-T cell therapy has shown success in treating certain malignancies, challenges such as resistance and non-durable efficacy remain. Strategies like NK cell therapy and haploidentical allografts are being explored as complementary treatments to achieve curative effects, especially in refractory cases.
Advancements in the field of cellular immunotherapy have accelerated in recent years and have changed the treatment landscape for a variety of hematologic malignancies. Cellular immunotherapy strategies exploit the patient's immune system to kill cancer cells. The successful use of CD19 chimeric antigen receptor (CAR) T-cells in treating B-cell malignancies is the paradigm of this revolution, and numerous ongoing studies are investigating and extending this approach to other malignancies. However, resistance to CAR-T cell therapy and non-durable efficacy have prevented CAR-T-cells from becoming the ultimate therapy. Because natural killer (NK) cells play an essential role in antitumor immunity, adoptively transferred allogeneic NK and CAR-modified NK cell therapy has been attempted in certain disease subgroups. Allogenic hematopoietic stem cell transplantation (allo-HSCT) is the oldest form of cellular immunotherapy and the only curative option for hematologic malignancies. Historically, the breadth of application of alloHSCT has been limited by a lack of identical sibling donors (ISDs). However, great strides have recently been made in the success of haploidentical allografts worldwide, which enable everyone to have a donor. Haploidentical donors can achieve comparable outcomes to those of ISDs and even better outcomes in certain circumstances because of a stronger graft vs. tumor effect. Currently, novel strategies such as CAR-T or NK-based immunotherapy can be applied as a complement to allo-HSCT for curative effects, particularly in refractory cases. Here, we introduce the developments in cellular immunotherapy in hematology.

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