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Ultra-low extracorporeal volume microfluidic leukapheresis is safe and effective in a rat model

Author

Listed:
  • Mubasher Iqbal

    (Department of Biomedical Engineering; University of Houston)

  • Alexandra L. McLennan

    (Department of Pediatrics; Baylor College of Medicine
    Center for Translational Research on Inflammatory Diseases; Michael E. DeBakey Veterans Affairs Medical Center)

  • Anton Mukhamedshin

    (Department of Biomedical Engineering; University of Houston)

  • Mai T. P. Dinh

    (Department of Biomedical Engineering; University of Houston)

  • Qisheng Liu

    (Center for Translational Research on Inflammatory Diseases; Michael E. DeBakey Veterans Affairs Medical Center
    Department of Medicine; Baylor College of Medicine)

  • Jacob J. Junco

    (Department of Pediatrics; Baylor College of Medicine)

  • Arvind Mohan

    (Department of Pediatrics; Baylor College of Medicine)

  • Poyyapakkam R. Srivaths

    (Department of Pediatrics; Baylor College of Medicine)

  • Karen R. Rabin

    (Department of Pediatrics; Baylor College of Medicine)

  • Thomas P. Fogarty

    (Department of Pediatrics; Baylor College of Medicine)

  • Sean C. Gifford

    (Halcyon Biomedical Incorporated)

  • Sergey S. Shevkoplyas

    (Department of Biomedical Engineering; University of Houston)

  • Fong W. Lam

    (Department of Pediatrics; Baylor College of Medicine
    Center for Translational Research on Inflammatory Diseases; Michael E. DeBakey Veterans Affairs Medical Center)

Abstract

Leukapheresis is a potentially life-saving therapy for children with symptomatic hyperleukocytosis. However, the standard centrifugation-based approach exposes pediatric patients to significant complications due to its large extracorporeal volume, high flow rates, and considerable platelet loss. Here, we tested whether performing cell separation with a high-throughput microfluidic technology could alleviate these limitations. In vitro, our microfluidic devices removed ~85% of large leukocytes and ~90% of spiked leukemic blasts from undiluted human whole blood, while minimizing platelet losses. Multiplexed devices connected in parallel allowed for faster, clinically relevant flow rates in vitro with no difference in leukocyte collection efficiency. When connected to Sprague-Dawley rats, the devices removed large leukocytes with ~80% collection efficiency, reducing the leukocyte count in recirculating blood by nearly half after a 3-hour procedure. Evaluation of plasma biomarkers and end-organ histology revealed no adverse effects compared to sham control. Overall, our study suggests that microfluidics-based leukapheresis is safe and effective at selectively removing leukocytes from circulation, with separation performance sufficiently high to ultimately enable low extracorporeal volume leukapheresis in children.

Suggested Citation

  • Mubasher Iqbal & Alexandra L. McLennan & Anton Mukhamedshin & Mai T. P. Dinh & Qisheng Liu & Jacob J. Junco & Arvind Mohan & Poyyapakkam R. Srivaths & Karen R. Rabin & Thomas P. Fogarty & Sean C. Giff, 2025. "Ultra-low extracorporeal volume microfluidic leukapheresis is safe and effective in a rat model," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57003-5
    DOI: 10.1038/s41467-025-57003-5
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    References listed on IDEAS

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    1. Fong Wilson Lam & Cameron August Brown & Christian Valladolid & Dabel Cynthia Emebo & Timothy Gerald Palzkill & Miguel Angel Cruz, 2020. "The vimentin rod domain blocks P-selectin-P-selectin glycoprotein ligand 1 interactions to attenuate leukocyte adhesion to inflamed endothelium," PLOS ONE, Public Library of Science, vol. 15(10), pages 1-18, October.
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