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Enumeration of Major Peripheral Blood Leukocyte Populations for Multicenter Clinical Trials Using a Whole Blood Phenotyping Assay
Published on: September 16, 2012
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.
Abstract:
Cryopreservation of peripheral blood leukocytes is widely used to preserve cells for immune response evaluations in clinical trials and offers many advantages for ease and standardization of immunological assessments, but detrimental effects of this process have been observed on some cell subsets, such as granulocytes, B cells, and dendritic cells. Assaying fresh leukocytes gives a more accurate picture of the in vivo state of the cells, but is often difficult to perform in the context of large clinical trials. Fresh cell assays are dependent upon volunteer commitments and timeframes and, if time-consuming, their application can be impractical due to the working hours required of laboratory personnel. In addition, when trials are conducted at multiple centers, laboratories with the resources and training necessary to perform the assays may not be located in sufficient proximity to clinical sites. To address these issues, we have developed an 11-color antibody staining panel that can be used with Trucount tubes (Becton Dickinson; San Jose, CA) to phenotype and enumerate the major leukocyte populations within the peripheral blood, yielding more robust cell-type specific information than assays such as a complete blood count (CBC) or assays with commercially-available panels designed for Trucount tubes that stain for only a few cell types. The staining procedure is simple, requires only 100 μl of fresh whole blood, and takes approximately 45 minutes, making it feasible for standard blood-processing labs to perform. It is adapted from the BD Trucount tube technical data sheet (version 8/2010). The staining antibody cocktail can be prepared in advance in bulk at a central assay laboratory and shipped to the site processing labs. Stained tubes can be fixed and frozen for shipment to the central assay laboratory for multicolor flow cytometry analysis. The data generated from this staining panel can be used to track changes in leukocyte concentrations over time in relation to intervention and could easily be further developed to assess activation states of specific cell types of interest. In this report, we demonstrate the procedure used by blood-processing lab technicians to perform staining on fresh whole blood and the steps to analyze these stained samples at a central assay laboratory supporting a multicenter clinical trial. The video details the procedure as it is performed in the context of a clinical trial blood draw in the HIV Vaccine Trials Network (HVTN).
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