Vacuum-Stabilized Palmar Cooling Mobilizes Circulating Small Pluripotent Stem Cells in Humans

Authors

  • Torbjörn Ogéus DC
  • PgD
  • MSc
  • ScA
  • Manuel Riegner
  • MD

Abstract

Background: Small Pluripotent Stem Cells (SPSCs) have been identified in adult peripheral blood and are characterized by their small size and expression of pluripotency-associated markers. Strategies that safely and reproducibly increase the availability of such cells without pharmacological intervention remain of interest for translational and regenerative applications.

Methods: In this paired pre–post observational study, 50 adult subjects (male and female, aged 20–67 years) underwent exposure to a standardized vacuum-based physiological stimulus using the Vacuul device. Peripheral blood samples were collected immediately before and after exposure. SPSCs were isolated using a size- and centrifugation-based enrichment protocol implemented within a standardized analytical framework. Cell concentration and viability were assessed using an automated cell counter, and immunocytochemical analyses were performed to evaluate expression of OCT4, SOX2, and SSEA-4, with Hoechst nuclear staining.

Results: Baseline SPSC concentration averaged approximately 20 × 10? cells/mL. Following Vacuul exposure, SPSC concentration increased by a mean of approximately 30%, with individual responses ranging from 12% to 55%. All subjects demonstrated an increase in circulating SPSC concentration. Cell viability remained stable at 98–99% before and after exposure. Immunocytochemical analysis demonstrated preserved expression of pluripotency-associated markers and consistent nuclear staining following Vacuul exposure.

Conclusions: Vacuum-Stabilized Palmar Cooling is associated with a reproducible increase in circulating SPSCs without compromising cell viability or altering pluripotency-associated marker expression.

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Published

2026-05-13

How to Cite

DC, T. O., PgD, MSc, ScA, Riegner, M., & MD. (2026). Vacuum-Stabilized Palmar Cooling Mobilizes Circulating Small Pluripotent Stem Cells in Humans. Archives of Clinical and Biomedical Research, 10(3), 162–172. Retrieved from https://fortunejournals.org/ojs/index.php/acbr/article/view/15179