The Impact of Mechanical Circulatory Support Devices on White Blood Cell Phenotype and Function
- PMID: 40251454
- DOI: 10.1007/s13239-025-00784-z
The Impact of Mechanical Circulatory Support Devices on White Blood Cell Phenotype and Function
Abstract
Background: Mechanical circulatory support devices (MCSDs) have gradually become an effective treatment of end-stage heart failure (HF). However, the introduction of foreign surfaces and non-physiological shear stress (NPSS) can cause severe damage to various blood cells, leading to impaired function of immune system and increased risk of complications such as inflammation and thrombosis. The effect of mechanical injury on white blood cell (WBC) has been largely neglected compared to that on red blood cell (RBC) and platelet (PLT).
Method: To better understand the impact of MCSDs on WBCs and emphasize the importance of investigating WBC damage to avoid adverse events during mechanical circulatory support, this review elaborated the induction of WBC phenotypic and functional injury by MCSD-related factors, and the relationship between injury and clinical complications. Furthermore, this article provided a detailed review and comparative analysis of in vitro blood-shearing devices (BSDs) and detection methods used in WBC damage investigation.
Results: NPSS, biomaterials and other related factors can activate WBC, decrease WBC function, and promote the release of pro-inflammatory and pro-thrombotic microparticles, increasing the risk of inflammation and thrombotic complications. The evaluation of WBC damage typically involves measuring cell viability and dysfunction using in vitro BSDs (e.g. concentric cylinder devices) and injury detection methods (e.g. flow cytometry).
Conclusions: WBCs with normal morphology may also experience functional failure due to NPSS from MCSDs, leading to sublethal mechanical cell injury. Therefore, the effect of MCSDs on WBCs can be more comprehensively evaluated by a combination of measuring cell functional capacity and cell counting.
Keywords: Detection methods; In Vitro blood-shearing devices; Inflammation; Leukocyte damage; Shear stress.
© 2025. The Author(s) under exclusive licence to Biomedical Engineering Society.
Conflict of interest statement
Declarations. Competing interests: The authors have no relevant financial or non-financial interests to disclose.
Similar articles
-
Microfluidic approaches for the assessment of blood cell trauma: a focus on thrombotic risk in mechanical circulatory support devices.Int J Artif Organs. 2016 Jun 15;39(4):184-93. doi: 10.5301/ijao.5000485. Epub 2016 Mar 30. Int J Artif Organs. 2016. PMID: 27034318
-
Mechanical shear stress and leukocyte phenotype and function: Implications for ventricular assist device development and use.Int J Artif Organs. 2019 Mar;42(3):133-142. doi: 10.1177/0391398818817326. Epub 2018 Dec 26. Int J Artif Organs. 2019. PMID: 30585115 Review.
-
In vitro comparative study of red blood cell and VWF damage on 3D printing biomaterials under different blood-contacting conditions.Proc Inst Mech Eng H. 2023 Aug;237(8):1029-1036. doi: 10.1177/09544119231186474. Epub 2023 Jul 7. Proc Inst Mech Eng H. 2023. PMID: 37417741
-
In vitro study of red blood cell and VWF damage in mechanical circulatory support devices based on blood-shearing platform.Proc Inst Mech Eng H. 2022 Jun;236(6):860-866. doi: 10.1177/09544119221088420. Epub 2022 Apr 3. Proc Inst Mech Eng H. 2022. PMID: 35369808
-
A review of implantable pulsatile blood pumps: Engineering perspectives.Int J Artif Organs. 2020 Sep;43(9):559-569. doi: 10.1177/0391398820902470. Epub 2020 Feb 10. Int J Artif Organs. 2020. PMID: 32037940 Review.
References
-
- Piperata A, Caraffa R, Avesani M, Gerosa G, Bottio T. Heart transplantation in the new era of extended donor criteria. Authorea Preprints. 2021.
-
- Mei X, Lu B, Wu P, Zhang L. In vitro study of red blood cell and VWF damage in mechanical circulatory support devices based on blood-shearing platform. Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine. 2022;236(6):860-6.
Publication types
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous