Abstract

Combining microfluidics technology with machine learning represents an innovative approach to conduct massive quantitative cell behavior study and implement smart decision-making systems in support of clinical diagnostics. The spleen plays a key-role in rare hereditary hemolytic anemia (RHHA), being the organ responsible for the premature removal of defective red blood cells (RBCs). The goal is to adapt the physiological spleen filtering strategy for in vitro study and monitoring of blood diseases through RBCs shape analysis. Then, a microfluidic device mimicking the slits of the spleen red pulp area and video data analysis are combined for the characterization of RBCs in RHHA. This microfluidic unit is designed to evaluate RBC deformability by maintaining them fixed in planar orientation, allowing the visual inspection of RBC’s capacity to restore their original shape after crossing microconstrictions. Then, two cooperative learning approaches are used for the analysis: the majority voting scheme, in which the most voted label for all the cell images is the class assigned to the entire video; and the maximum sum of scores to decide the maximally scored class to assign. The proposed platform shows the capability to discriminate healthy controls and patients with an average efficiency of 91%, but also to distinguish between RHHA subtypes, with an efficiency of 82%.

Highlights

  • Combining microfluidics technology with machine learning represents an innovative approach to conduct massive quantitative cell behavior study and implement smart decision-making systems in support of clinical diagnostics

  • Defects affecting red blood cells (RBCs) can lead to rare hereditary hemolytic anemia (RHHA), a group of heterogeneous inherited disorders characterized by premature removal of RBCs in the spleen, as they are not able to pass through the Inter Endothelial Slits (IES)

  • We propose a microfluidic platform that mimics the flow conditions of the spleen in the IES region, combined with image analysis based on deep learning algorithms for the massive and objective study of RBCs deformation properties with the aim to distinguish between specific types of RHHA, using for our study human blood samples from healthy donors and from patients (SCD, thalassemia syndromes (THAL), and hereditary spherocytosis (HS))

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Summary

Introduction

Combining microfluidics technology with machine learning represents an innovative approach to conduct massive quantitative cell behavior study and implement smart decision-making systems in support of clinical diagnostics. The spleen plays a key-role in rare hereditary hemolytic anemia (RHHA), being the organ responsible for the premature removal of defective red blood cells (RBCs). A microfluidic device mimicking the slits of the spleen red pulp area and video data analysis are combined for the characterization of RBCs in RHHA This microfluidic unit is designed to evaluate RBC deformability by maintaining them fixed in planar orientation, allowing the visual inspection of RBC’s capacity to restore their original shape after crossing microconstrictions. Human RBCs are 120-day lifespan cells, known for containing hemoglobin (Hb), necessary to accomplish their main function as oxygen transporters They have a diameter and thickness of 8 and 2–3 μm, respectively, presenting a unique flexibility characteristic needed to rapidly deform themselves and squeeze into the blood flow; into the capillaries which diameter can reach half of the size of an R­ BC3,4. Techniques as ectacytometry, that gives a results as a mean value, use whole or diluted blood and do not consider samples’ heterogeneity and difference in size among R­ BCs15

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