Multimodal spatial proteomic profiling in acute myeloid leukemia

Acute myeloid leukemia (AML) resides in an immune-rich microenvironment, yet, immune-based therapies have faltered in eliciting durable responses. Bridging this paradox requires a comprehensive understanding of leukemic interactions within the bone marrow microenvironment. We optimized a high-throughput tissue-microarray-based pipeline for high-plex spatial immunofluorescence and mass cytometry imaging on a single slide, capturing immune, tumor, and structural components. Using unbiased clustering on the spatial K function, we unveiled the presence of tertiary lymphoid-like aggregates in bone marrow, which we validated using spatial transcriptomics and an independent proteomics approach. We then found validated TLS signatures predictive of outcomes in AML using an integrated public 480-patient transcriptomic dataset. By harnessing high-plex spatial proteomics, we open the possibility of discovering novel structures and interactions that underpin leukemic immune response. Further, our study's methodologies and resources can be adapted for other bone marrow diseases where decalcification and autofluorescence present challenges.

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Publication Details

Journal
npj Precision Oncology
Published
2025-05-20
DOI
https://doi.org/10.1038/s41698-025-00897-7
Citations
3
Primary Topic
Advanced Biosensing Techniques and Applications
Type
article
Field-Weighted Citation Impact
2.42

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article

Multimodal spatial proteomic profiling in acute myeloid leukemia

Taghi Manshouri, Carlos E. Bueso‐Ramos, Jared K. Burks, Christopher D. Pacheco et al.
3 citations
npj Precision Oncology
Advanced Biosensing Techniques and Applications
2.42
article

Multimodal spatial proteomic profiling in acute myeloid leukemia

Taghi Manshouri, Carlos E. Bueso‐Ramos, Jared K. Burks, Christopher D. Pacheco, Ivo Veletić, Miriam B. Garcia, Patrick K. Reville, Andres Quesada, Jessica L. Root, Christopher Ly, Branko Cuglievan, Sonali Jindal, Sammy Ferri‐Borgogno, Javier A. Gomez, Padmanee Sharma, Fatima Zahra Jelloul, Hussein A. Abbas, Enes Dasdemir, Sreyashi Basu, Akshay Basi
article en
3 citations

Abstract

Acute myeloid leukemia (AML) resides in an immune-rich microenvironment, yet, immune-based therapies have faltered in eliciting durable responses. Bridging this paradox requires a comprehensive understanding of leukemic interactions within the bone marrow microenvironment. We optimized a high-throughput tissue-microarray-based pipeline for high-plex spatial immunofluorescence and mass cytometry imaging on a single slide, capturing immune, tumor, and structural components. Using unbiased clustering on the spatial K function, we unveiled the presence of tertiary lymphoid-like aggregates in bone marrow, which we validated using spatial transcriptomics and an independent proteomics approach. We then found validated TLS signatures predictive of outcomes in AML using an integrated public 480-patient transcriptomic dataset. By harnessing high-plex spatial proteomics, we open the possibility of discovering novel structures and interactions that underpin leukemic immune response. Further, our study's methodologies and resources can be adapted for other bone marrow diseases where decalcification and autofluorescence present challenges.

npj Precision OncologyVol. 9(1)
The University of Texas MD Anderson Cancer Center (US), University of Houston (US)
Cancer Prevention and Research Institute of Texas, National Institutes of Health, University of Texas MD Anderson Cancer Center, National Cancer Institute
Openalex Percentile: Top 12%
Advanced Biosensing Techniques and Applications
2.42
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