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An at-home blood collection device for remote immune monitoring by high-parameter flow cytometry
Andrew J. Konecny, Fang Yun Lim, Eva Domenjo-Vila, Erika Lovas, Rachel L. Blazevic, Louise E. Kimball, Michael Boeckh, Alpana Waghmare, Martin Prlic
Andrew J. Konecny, Fang Yun Lim, Eva Domenjo-Vila, Erika Lovas, Rachel L. Blazevic, Louise E. Kimball, Michael Boeckh, Alpana Waghmare, Martin Prlic
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Research Article Cell biology Clinical Research Immunology

An at-home blood collection device for remote immune monitoring by high-parameter flow cytometry

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Abstract

At-home blood collection devices (ABCDs) can facilitate study participation for remote and rural cohorts. Previous studies used ABCDs to interrogate samples by proteomics and sequencing approaches. We wanted to address the question of whether this approach could be used to assess live immune cells with high-parameter flow cytometry to enable remote immune monitoring. We first compared blood from standard venipuncture with ABCD blood draws, followed by assessment of the impact of sample shipping on immune cell viability and phenotyping. We found that capillary blood collected with a Tasso+ device and concurrently drawn venipuncture blood samples had highly congruent immune cell composition and phenotype. Shipment of Tasso+ samples via the United States Postal Service altered the myeloid compartment, but T cell numbers, subsets, and phenotypes remained remarkably stable compared with non-shipped samples. Finally, we describe a flow cytometry analysis framework that allowed for direct sample comparison even when samples were stained and analyzed over a time period of 1.5 years. Overall, our data highlight the feasibility of using ABCDs combined with subsequent flow cytometry analysis for remote immune monitoring. Additionally, our study also identifies areas that could be improved to further promote the use of ABCDs for immune monitoring.

Authors

Andrew J. Konecny, Fang Yun Lim, Eva Domenjo-Vila, Erika Lovas, Rachel L. Blazevic, Louise E. Kimball, Michael Boeckh, Alpana Waghmare, Martin Prlic

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Figure 6

Cytometry controls allow for reproducible assessment for long-term longitudinal studies.

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Cytometry controls allow for reproducible assessment for long-term longi...
(A) Overview of cytometry controls used to determine optimization and standardization of machine settings, and reagent or assay performance. (B and C) Representative plot of 6-peak Ultra Rainbow Calibration Particle raw fluorescence in the PE detector (B) and quantification of raw fluorescence of peaks 4, 5, and 6 across all detectors (C). Acquisitions took place across 2 years (reference in black and 8 subsequent acquisitions on separate days in color, n = 9). (D and E) Representative plot of T cell and B cell gating with frequencies of CD45+ non-neutrophils (D) and quantification of all major immune cell lineage frequencies among CD45+ non-neutrophils in the same biological replicate PBMC (E) (biological replicate stained on 10 separate days and acquired on 8 separate days, n = 10). (F) Representative plot of CD32, CD86, and SIRPα on cDCs. Color coding in F matches dates of staining in D. T cells included in F from September 11, 2023 with staining in gray for histograms as a negative cell population control. (G) Quantification of all phenotyping markers on cDCs (n = 10).

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