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Development and optimization of a diluted whole blood ELISpot assay to test immune function.
Ungaro, Ricardo F; Xu, Julie; Kucaba, Tamara A; Rao, Mahil; Bergmann, Christian B; Brakenridge, Scott C; Efron, Philip A; Goodman, Michael D; Gould, Robert W; Hotchkiss, Richard S; Liang, Muxuan; Mazer, Monty B; McGonagill, Patrick W; Moldawer, Lyle L; Remy, Kenneth E; Turnbull, Isaiah R; Caldwell, Charles C; Badovinac, Vladimir P; Griffith, Thomas S.
Afiliación
  • Ungaro RF; Sepsis and Critical Illness Research Center and Department of Surgery, University of Florida College of Medicine, Gainesville, FL, United States of America.
  • Xu J; Department of Urology, University of Minnesota, Minneapolis, MN, United States of America.
  • Kucaba TA; Department of Urology, University of Minnesota, Minneapolis, MN, United States of America.
  • Rao M; Department of Pediatrics, University of Iowa, Iowa City, IA, United States of America.
  • Bergmann CB; University Hospital Ulm, Clinic for Trauma Surgery, Hand, Plastic, and Reconstructive Surgery Albert-Einstein-Allee 23, Ulm, Germany.
  • Brakenridge SC; Department of Surgery, University of Washington, Seattle, WA, United States of America.
  • Efron PA; Sepsis and Critical Illness Research Center and Department of Surgery, University of Florida College of Medicine, Gainesville, FL, United States of America.
  • Goodman MD; Department of Surgery, University of Cincinnati, Cincinnati, OH, United States of America.
  • Gould RW; Department of Anesthesiology, University of Minnesota, Minneapolis, MN, United States of America.
  • Hotchkiss RS; Department of Anesthesiology, Washington University, St. Louis, MO, United States of America.
  • Liang M; Department of Biostatistics, University of Florida, Gainesville, FL, United States of America.
  • Mazer MB; Department of Pediatrics, UH Rainbow Babies and Children's Hospital, Cleveland, OH, United States of America.
  • McGonagill PW; Department of Surgery, University of Iowa, Iowa City, IA, United States of America.
  • Moldawer LL; Sepsis and Critical Illness Research Center and Department of Surgery, University of Florida College of Medicine, Gainesville, FL, United States of America.
  • Remy KE; Department of Pediatrics, UH Rainbow Babies and Children's Hospital, Cleveland, OH, United States of America.
  • Turnbull IR; Department of Anesthesiology, Washington University, St. Louis, MO, United States of America; Immune Functional Diagnostics, LLC, St. Louis, MO, United States of America.
  • Caldwell CC; Department of Surgery, University of Cincinnati, Cincinnati, OH, United States of America.
  • Badovinac VP; Department of Pathology, University of Iowa, Iowa City, IA, United States of America.
  • Griffith TS; Department of Urology, University of Minnesota, Minneapolis, MN, United States of America; Center for Immunology, University of Minnesota, Minneapolis, MN, United States of America; Minneapolis VA Health Care System, Minneapolis, MN, United States of America. Electronic address: tgriffit@umn.edu.
J Immunol Methods ; 533: 113743, 2024 Oct.
Article en En | MEDLINE | ID: mdl-39147231
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interferón gamma / Factor de Necrosis Tumoral alfa / Sepsis / Ensayo de Immunospot Ligado a Enzimas Límite: Female / Humans / Male Idioma: En Revista: J Immunol Methods Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interferón gamma / Factor de Necrosis Tumoral alfa / Sepsis / Ensayo de Immunospot Ligado a Enzimas Límite: Female / Humans / Male Idioma: En Revista: J Immunol Methods Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos