Development and optimization of a diluted whole blood ELISpot assay to test immune function

Sepsis remains a leading cause of death worldwide with no proven immunomodulatory therapies. Stratifying Patient Immune Endotypes in Sepsis ('SPIES') is a prospective, multicenter observational study testing the utility of ELISpot as a functional bioassay specifically measuring cytokine-producing cells after stimulation to identify the immunosuppressed endotype, predict clinical outcomes in septic patients, and test potential immune stimulants for clinical development. Most ELISpot protocols call for the isolation of PBMC prior to their inclusion in the assay. In contrast, we developed a diluted whole blood (DWB) ELISpot protocol that has been validated across multiple laboratories. Heparinized whole blood was collected from healthy donors and septic patients and tested under different stimulation conditions to evaluate the impact of blood dilution, stimulant concentration, blood storage, and length of stimulation on ex vivo IFNγ and TNFα production as measured by ELISpot. We demonstrate a dynamic range of whole blood dilutions that give a robust ex vivo cytokine response to stimuli. Additionally, a wide range of stimulant concentrations can be utilized to induce cytokine production. Further modifications demonstrate anticoagulated whole blood can be stored up to 24 h at room temperature without losing significant functionality. Finally, we show ex vivo stimulation can be as brief as 4 h allowing for a substantial decrease in processing time. The data demonstrate the feasibility of using ELISpot to measure the functional capacity of cells within DWB under a variety of stimulation conditions to inform clinicians on the extent of immune dysregulation in septic patients.

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Publication Details

Journal
Journal of Immunological Methods
Published
2024-08-13
DOI
https://doi.org/10.1016/j.jim.2024.113743
Citations
3
Primary Topic
Sepsis Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
1.16

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article

Development and optimization of a diluted whole blood ELISpot assay to test immune function

Richard S. Hotchkiss, Isaiah R. Turnbull, Mahil Rao, Philip A. Efron et al.
3 citations
Journal of Immunological Methods
Sepsis Diagnosis and Treatment
1.16
article

Development and optimization of a diluted whole blood ELISpot assay to test immune function

Richard S. Hotchkiss, Isaiah R. Turnbull, Mahil Rao, Philip A. Efron, Patrick W. McGonagill, Julie Xu, Charles C. Caldwell, R. W. Gould, Tamara A. Kucaba, Christian B. Bergmann, Thomas S. Griffith, Michael D. Goodman, Lyle L. Moldawer, Kenneth E. Remy, Muxuan Liang, Ricardo Ungaro, Monty B. Mazer, Scott C. Brakenridge, Vladimir P. Badovinac
article en
3 citations

Abstract

Sepsis remains a leading cause of death worldwide with no proven immunomodulatory therapies. Stratifying Patient Immune Endotypes in Sepsis ('SPIES') is a prospective, multicenter observational study testing the utility of ELISpot as a functional bioassay specifically measuring cytokine-producing cells after stimulation to identify the immunosuppressed endotype, predict clinical outcomes in septic patients, and test potential immune stimulants for clinical development. Most ELISpot protocols call for the isolation of PBMC prior to their inclusion in the assay. In contrast, we developed a diluted whole blood (DWB) ELISpot protocol that has been validated across multiple laboratories. Heparinized whole blood was collected from healthy donors and septic patients and tested under different stimulation conditions to evaluate the impact of blood dilution, stimulant concentration, blood storage, and length of stimulation on ex vivo IFNγ and TNFα production as measured by ELISpot. We demonstrate a dynamic range of whole blood dilutions that give a robust ex vivo cytokine response to stimuli. Additionally, a wide range of stimulant concentrations can be utilized to induce cytokine production. Further modifications demonstrate anticoagulated whole blood can be stored up to 24 h at room temperature without losing significant functionality. Finally, we show ex vivo stimulation can be as brief as 4 h allowing for a substantial decrease in processing time. The data demonstrate the feasibility of using ELISpot to measure the functional capacity of cells within DWB under a variety of stimulation conditions to inform clinicians on the extent of immune dysregulation in septic patients.

Journal of Immunological MethodsVol. 533
University of Iowa (US), University of Minnesota (US), Universität Ulm (DE), University of Washington (US), Washington University in St. Louis (US), University of Florida (US), Minneapolis VA Health Care System (US), MNGI Digestive Health (US), Rainbow Babies & Children's Hospital (US), University Hospital Ulm (DE), University of Cincinnati (US)
U.S. Department of Veterans Affairs, University of Iowa, National Institutes of Health
Zero hunger
Openalex Percentile: Top 20%
Sepsis Diagnosis and Treatment
1.16
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