High-dimensional Immune Profiles and Machine Learning May Predict Acute Myeloid Leukemia Relapse Early following Transplant

被引:0
作者
Short, Samantha M. [1 ]
Perez, Mildred D. [1 ]
Morse, Alexis E. [1 ]
Jennings, Rebecca Damron [2 ,4 ]
Howard, Dianna S. [2 ]
Foureau, David [3 ]
Chojecki, Aleksander
David, Camille [1 ]
Blaha, Lauren [1 ]
Shaw, Yolanda [1 ]
Lee, C. Jiah [1 ]
Park, Nuri [1 ]
Marsac, Caitlyn [1 ]
Agostino, Ralph [5 ]
Khuri, Natalia [6 ]
Grayson, Jason M. [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Microbiol & Immunol, Winston Salem, NC USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Sect Hematol & Oncol, One Med Ctr Blvd, Winston Salem, NC USA
[3] Atrium Hlth, Levine Canc Inst, Immune Monitoring Core Lab, Charlotte, NC USA
[4] Atrium Hlth, Levine Canc Inst, Dept Hematol Oncol & Blood Disorders, Charlotte, NC USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Biostat & Data Sci, One Med Ctr Blvd, Winston Salem, NC USA
[6] Wake Forest Univ, Dept Comp Sci, Winston Salem, NC USA
关键词
CELLS;
D O I
10.4049/jimmunol.2300827
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Identification of early immune signatures associated with acute myeloid leukemia (AML) relapse following hematopoietic stem cell transplant (HSCT) is critical for patient outcomes. We analyzed PBMCs from 58 patients with AML undergoing HSCT, focusing on T cell subsets and functional profiles. High-dimensional flow cytometry coupled with Uniform Manifold Approximation and Projection dimensionality reduction and PhenoGraph clustering revealed distinct changes in CD4+ and CD8+ T cell populations in 16 patients who relapsed within 1 y of HSCT. We observed increased IL-2, IL-10, and IL-17-producing supervised machine learning algorithm that predicted AML relapse with 90% accuracy within 30 d after HSCT using highthroughput assays. The algorithm leverages condensed immune phenotypic data, alongside the ADASYN algorithm, for data balancing and 100 rounds of XGBoost supervised learning. This approach holds potential for detecting relapse-associated immune signatures months before clinical manifestation. Our findings demonstrate a distinct immunological signature potentially capable of predicting AML relapse as early as 30 d after HSCT. The Journal of Immunology, 2024, 213: 1441-1451.
引用
收藏
页码:1441 / 1451
页数:12
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