Enumeration of major peripheral blood leukocyte populations for multicenter clinical trials using a whole blood

Tiffany R Hensley1, Austin B Easter, Sarah E Gerdts

  • 1Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center.

Insights

Cryopreservation of blood cells can alter immune cell subsets. This study presents a rapid, 11-color flow cytometry assay for fresh leukocytes, enabling accurate immune monitoring in large clinical trials.

Area of Science:

  • Immunology
  • Clinical Trials
  • Flow Cytometry

Background:

  • Cryopreservation of peripheral blood leukocytes is standard for immune response evaluation but can negatively impact certain cell subsets.
  • Assessing fresh leukocytes provides a more accurate in vivo snapshot but is logistically challenging for large, multicenter clinical trials due to time and location constraints.

Purpose of the Study:

  • To develop a standardized, rapid, and robust method for phenotyping and enumerating major peripheral blood leukocyte populations in fresh blood samples.
  • To provide a feasible alternative to cryopreservation for immunological assessments in multicenter clinical trials.

Main Methods:

  • Development of an 11-color antibody staining panel for use with Trucount tubes.
  • Procedure requires 100 μl of fresh whole blood and takes approximately 45 minutes.
  • Stained samples can be fixed, frozen, and shipped for central multicolor flow cytometry analysis.

Main Results:

  • The developed assay provides more robust cell-type specific information compared to complete blood counts or limited commercial panels.
  • The staining procedure is simple and adaptable for standard blood-processing laboratories.
  • The method allows for bulk preparation of antibody cocktails and centralized analysis, facilitating multicenter trial logistics.

Conclusions:

  • This 11-color flow cytometry assay offers a practical and accurate method for monitoring leukocyte populations in fresh blood for clinical trials.
  • The assay overcomes limitations of cryopreservation and logistical challenges of fresh sample analysis in multicenter settings.
  • The method can be further expanded to assess immune cell activation states, enhancing its utility in clinical research.

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