Hematology · 2 h ago
Review calls for multidimensional assessment of T-cell function in AML
A review in BMC Medicine argues that inhibitory-receptor expression alone does not adequately characterize T-cell dysfunction in acute myeloid leukemia (AML). The authors propose assessing several functional, metabolic and cellular features, emphasizing that T-cell states in AML are heterogeneous and context dependent.
- Inhibitory-receptor expression alone may not capture T-cell function.
- The review proposes a multidimensional assessment framework.
- T-cell impairment in AML appears heterogeneous and context dependent.
T-cell exhaustion or dysfunction has been linked to AML relapse, particularly after allogeneic hematopoietic stem cell transplantation. In this review, researchers examine how the AML tumor microenvironment may affect T cells and argue that assessments based only on inhibitory receptors such as PD-1, TIM-3, LAG-3 and CTLA-4 provide an incomplete account of their function. The article is a review and reports no new patient data.
The authors propose a broader characterization that includes cytokine secretion, cytotoxic capacity, activation and proliferation, metabolic profile, T-cell subsets, telomere length and epigenetic state. They also highlight evidence that T cells in AML are not uniformly impaired: some may retain cytotoxic potential, while dysfunction varies with cellular context and the tumor microenvironment.
The authors argue that standardized, multidimensional profiling could inform research into the design and timing of T-cell-based therapies. The review does not establish a validated assessment standard or demonstrate that adopting this approach improves patient outcomes; its proposals require further evaluation.
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BMC Medicine: T cells in AML: are they functionally impaired? a call for comprehensive characterization ↗This is an automated AI-condensed summary that has not yet been reviewed by an editor. Always consult the full item at the original source.
