Cryopreservation reduces the concentration of detectable bacteria in contaminated peripheral blood progenitor cell

Frank Kipp1, Elmar Linnemann, Rudolf-Josef Fischer

  • 1Institute of Medical Microbiology, the Institute of Transfusion Medicine/Transplantation Immunology, and the Department of Biometrics, University Hospital Münster, Germany.

Transfusion
|July 1, 2004
PubMed
Abstract

Insights

Cryopreservation of peripheral blood progenitor cell products (PBPCPs) reduces detectable bacterial contamination. This finding is crucial for accurate sterility testing of PBPCPs to prevent false-negative results and ensure patient safety.

Area of Science:

  • Microbiology
  • Hematology
  • Cell Therapy

Background:

  • Microbial contamination of peripheral blood progenitor cell products (PBPCPs) poses significant clinical risks.
  • Ensuring the sterility of PBPCPs is critical for patient safety in cell transplantation.

Purpose of the Study:

  • To investigate the impact of cryopreservation on the detection sensitivity of bacterial contamination in PBPCPs.
  • To assess how cryopreservation affects the recovery of common bacterial contaminants like Staphylococcus epidermidis and Escherichia coli.

Main Methods:

  • Expired PBPCPs were artificially contaminated with known concentrations of S. epidermidis or E. coli.
  • Bacterial concentrations (CFUs/mL) were quantified before and after a 24-hour cryopreservation period.
  • Standard microbiological culture techniques were employed for bacterial enumeration.

Main Results:

  • A statistically significant decrease in detectable Staphylococcus epidermidis was observed post-cryopreservation (2529 CFUs/mL vs. 2182 CFUs/mL, p < 0.05).
  • Similarly, Escherichia coli counts showed a significant reduction after cryopreservation (424 CFUs/mL vs. 343 CFUs/mL, p < 0.05).

Conclusions:

  • Cryopreservation demonstrably reduces the concentration of detectable bacteria in contaminated PBPCPs.
  • This reduction may lead to false-negative results in sterility testing, particularly for samples with low bacterial loads.
  • Clinical implications include potential risks associated with administering contaminated PBPCPs due to compromised sterility assessment.

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