AI Article Synopsis

  • Acute myeloid leukemia (AML) remains difficult to treat despite new therapies, highlighting the need for effective immune responses against the disease.
  • The review emphasizes various immunotherapy targets, including both cancer cell features and the surrounding environment, and suggests personalized treatment strategies.
  • Key immunotherapy methods discussed include immune checkpoint inhibitors, antibody-drug conjugates, therapeutic vaccines, and CAR-T/NK cells, while also addressing resistance mechanisms and the impact of the leukemia microenvironment on treatment outcomes.

Article Abstract

Despite advancements, acute myeloid leukemia (AML) remains unconquered by current therapies. Evidence of immune evasion during AML progression, such as HLA loss and T-cell exhaustion, suggests that antileukemic immune responses contribute to disease control and could be harnessed by immunotherapy. In this review, we discuss a spectrum of AML immunotherapy targets, encompassing cancer cell-intrinsic and surface antigens as well as targeting in the leukemic milieu, and how they can be tailored for personalized approaches. These targets are overviewed across major immunotherapy modalities applied to AML: immune checkpoint inhibitors, antibody-drug conjugates, therapeutic vaccines, bispecific/trispecific antibodies, and chimeric antigen receptor (CAR)-T and CAR-NK cells. Significance: Immune therapies in AML treatment show evolving promise. Ongoing research aims to customize approaches for varied patient profiles and clinical scenarios. This review covers immune surveillance mechanisms, therapy options like checkpoint inhibitors, antibodies, CAR-T/NK cells, and vaccines, as well as resistance mechanisms and microenvironment considerations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11215380PMC
http://dx.doi.org/10.1158/2643-3230.BCD-23-0202DOI Listing

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