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Clinical Trial Summary

The expression of mHLA-DR, measured by flow cytometry, is today the reference marker to guide immunostimulatory therapies (IFN-γ) in the most severely immunocompromised patients. Nevertheless, pre-analytical constraints (storage of samples at +4°C before analysis) limit the wide use of mHLA-DR in clinical practice (problem of transporting samples to sites with a flow cytometer). Recent studies have shown that samples taken on Cyto-Chex Blood Collection Tubes (BCT) (containing a cell membrane stabilizer) were, for mHLA-DR, stable at room temperature during 72 hours after sampling. The main objective of this study is to compare the expression of mHLA-DR from samples taken simultaneously from standard tubes (EDTA) and new generation Cyto-Chex BCT tubes, to validate using Cyto Chex BCT tube in the clinical practice. The investigators think that mHLA-DR quantification performed from Cyto-Chex BCT tubes is reliable and similar to quantification performed from EDTA tubes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05546632
Study type Observational
Source Hospices Civils de Lyon
Contact Anne-Claire LUKASZEWICZ, Professor
Phone + 33 (4 )72 11 13 27
Email Anne-claire.lukaszewicz@chu-lyon.fr
Status Recruiting
Phase
Start date October 13, 2022
Completion date November 13, 2022

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