4.6 Article

Patient-specific Immune States before Surgery Are Strong Correlates of Surgical Recovery

期刊

ANESTHESIOLOGY
卷 123, 期 6, 页码 1241-1255

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/ALN.0000000000000887

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资金

  1. Stanford Bio-X graduate research fellowship (Stanford, California)
  2. U.S. National Institutes of Health (NIH), Bethesda, Maryland [T32GM007276]
  3. U.S. NIH [1K23GM111657-01, T32GM089626, U19 AI057229, U54CA149145, N01-HV-00242, 1U19AI100627, 5R01AI07372405, R01CA184968, 1 R33 CA183654, R33 CA183692, 1R01GM10983601, 201303028, 1R01NS08953301]
  4. Ann Schreiber Mentored Investigator Award from the Ovarian Cancer Research Fund, New York, New York [OCRF 292495]
  5. Canadian Institute of Health Research, Ottawa, Ontario, Canada [CIHR 321510]
  6. International Society for Advancement of Cytometry Scholarship, Bethesda, Maryland
  7. NIH-the Baylor Research Institute, Dallas, Texas [41000411217]
  8. NIH-Northrop Grumman Corp., Falls Church, California [7500108142]
  9. California Institute for Regenerative Medicine, San Francisco, California [DR1-01477]
  10. U.S. Department of Defense, Washington, D.C. [OC110674]
  11. European Commission, Brussels, Belgium [Health.2010.1.2-1]
  12. U.S. Food and Drug Administration, Silver Spring, Maryland [HHSF223201210194C]
  13. Bill and Melinda Gates Foundation, Seattle, Washington [OPP 1017093, OPP1113682]
  14. Alliance for Lupus Research (New York, New York)
  15. Lymphoma Research Foundation, New York, New York
  16. Entertainment Industry Foundation (National Women's Cancer Research Alliance grant, Los Angeles, California)
  17. Stanford University Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford, California

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Background: Recovery after surgery is highly variable. Risk-stratifying patients based on their predicted recovery profile will afford individualized perioperative management strategies. Recently, application of mass cytometry in patients undergoing hip arthroplasty revealed strong immune correlates of surgical recovery in blood samples collected shortly after surgery. However, the ability to interrogate a patient's immune state before surgery and predict recovery is highly desirable in perioperative medicine. Methods: To evaluate a patient's presurgical immune state, cell-type-specific intracellular signaling responses to ex vivo ligands (lipopolysaccharide, interleukin [IL]-6, IL-10, and IL-2/granulocyte macrophage colony-stimulating factor) were quantified by mass cytometry in presurgical blood samples. Selected ligands modulate signaling processes perturbed by surgery. Twenty-three cell surface and 11 intracellular markers were used for the phenotypic and functional characterization of major immune cell subsets. Evoked immune responses were regressed against patient-centered outcomes, contributing to protracted recovery including functional impairment, postoperative pain, and fatigue. Results: Evoked signaling responses varied significantly and defined patient-specific presurgical immune states. Eighteen signaling responses correlated significantly with surgical recovery parameters (|R| = 0.37 to 0.70; false discovery rate < 0.01). Signaling responses downstream of the toll-like receptor 4 in cluster of differentiation (CD) 14(+) monocytes were particularly strong correlates, accounting for 50% of observed variance. Immune correlates identified in presurgical blood samples mirrored correlates identified in postsurgical blood samples. Conclusions: Convergent findings in pre- and postsurgical analyses provide validation of reported immune correlates and suggest a critical role of the toll-like receptor 4 signaling pathway in monocytes for the clinical recovery process. The comprehensive assessment of patients' preoperative immune state is promising for predicting important recovery parameters and may lead to clinical tests using standard flow cytometry.

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