Literature DB >> 22683728

Programmed death 1 expression as a marker for immune and physiological dysfunction in the critically ill surgical patient.

Sean F Monaghan1, Rajan K Thakkar, Mai L Tran, Xin Huang, William G Cioffi, Alfred Ayala, Daithi S Heffernan.   

Abstract

Programmed death 1 (PD-1) is an inhibitor protein receptor for the immune system and has been shown to be upregulated in animal models of critical illness as well as after trauma and in burn victims in humans. It is believed that PD-1 may play a role in the immune dysfunction seen in surgical critical illness. However, although prior studies have associated changes in PD-1 expression with altered immune cell function, it is not known if a correlation with clinical status exists. We therefore aimed to describe a potential role for PD-1 in the immune dysfunction seen in critically ill trauma and surgical patients. This is an observational cohort study. Acute Physiology and Chronic Health Evaluation II (APACHE II) scores were calculated on critically ill and injured trauma and surgical intensive care unit patients from a tertiary care/level I trauma center. Blood was drawn within 24 h of establishment of diagnosis and admission to the intensive care unit to measure circulating cytokine levels, as well as PD-1 expression on circulating cells. Main outcome measures included PD-1 expression on leukocytes and the relationship to physiological dysfunction (APACHE II) as well as the correlation of PD-1 expression and interleukin 10 levels among patients with severe physiological dysfunction. Samples were collected from 90 critically ill surgical patients. Among patients with severe physiological dysfunction (APACHE II >20), there were increased numbers of granulocytes (median, 144 vs. 90 cells/μL; P = 0.037) and monocytes (median, 12 vs. 6 cells/μL; P = 0.022) with PD-1 expression. In addition, among patients with an APACHE II score of greater than 20, there was a larger percentage of CD3 cells (44% vs. 29%; P = 0.015) expressing PD-1. When only patients with an APACHE II score greater than 20 were assessed, PD-1 expression on monocytes correlated positively with interleukin levels in the serum (r = 0.525, P = 0.05). Variability in the expression of PD-1 on leukocytes in critical surgical illness correlates with physiological dysfunction and suggests that PD-1 may be a valuable tool in the assessment of immune dysfunction following trauma or severe surgical insult.

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Year:  2012        PMID: 22683728     DOI: 10.1097/SHK.0b013e31825de6a3

Source DB:  PubMed          Journal:  Shock        ISSN: 1073-2322            Impact factor:   3.454


  30 in total

1.  Sepsis erodes CD8+ memory T cell-protective immunity against an EBV homolog in a 2B4-dependent manner.

Authors:  Jianfeng Xie; Rebecca L Crepeau; Ching-Wen Chen; Wenxiao Zhang; Shunsuke Otani; Craig M Coopersmith; Mandy L Ford
Journal:  J Leukoc Biol       Date:  2019-01-09       Impact factor: 4.962

2.  Inflammatory mechanisms in sepsis: elevated invariant natural killer T-cell numbers in mouse and their modulatory effect on macrophage function.

Authors:  Daithi S Heffernan; Sean F Monaghan; Rajan K Thakkar; Mai L Tran; Chun-Shiang Chung; Stephen H Gregory; William G Cioffi; Alfred Ayala
Journal:  Shock       Date:  2013-08       Impact factor: 3.454

3.  Increased attrition of memory T cells during sepsis requires 2B4.

Authors:  Jianfeng Xie; Ching-Wen Chen; Yini Sun; Sonia J Laurie; Wenxiao Zhang; Shunsuke Otani; Gregory S Martin; Craig M Coopersmith; Mandy L Ford
Journal:  JCI Insight       Date:  2019-05-02

4.  Effect of PD-1: PD-L1 in Invariant Natural Killer T-Cell Emigration and Chemotaxis Following Sepsis.

Authors:  John S Young; Daithi S Heffernan; Chun-Shiang Chung; Maude L Kettenmann; Whitney A Young; Valeria Sanabria Guillen; William G Cioffi; Alfred Ayala
Journal:  Shock       Date:  2016-05       Impact factor: 3.454

5.  Improved survival after induction of sepsis by cecal slurry in PD-1 knockout murine neonates.

Authors:  Whitney A Young; Eleanor A Fallon; Daithi S Heffernan; Philip A Efron; William G Cioffi; Alfred Ayala
Journal:  Surgery       Date:  2016-12-21       Impact factor: 3.982

Review 6.  Dysregulated myelopoiesis and hematopoietic function following acute physiologic insult.

Authors:  Tyler J Loftus; Alicia M Mohr; Lyle L Moldawer
Journal:  Curr Opin Hematol       Date:  2018-01       Impact factor: 3.284

Review 7.  A novel role for coinhibitory receptors/checkpoint proteins in the immunopathology of sepsis.

Authors:  Eleanor A Fallon; Bethany M Biron-Girard; Chun-Shiang Chung; Joanne Lomas-Neira; Daithi S Heffernan; Sean F Monaghan; Alfred Ayala
Journal:  J Leukoc Biol       Date:  2018-02-02       Impact factor: 4.962

8.  Flt3 Ligand Treatment Attenuates T Cell Dysfunction and Improves Survival in a Murine Model of Burn Wound Sepsis.

Authors:  Naeem K Patil; Julia K Bohannon; Liming Luan; Yin Guo; Benjamin Fensterheim; Antonio Hernandez; Jingbin Wang; Edward R Sherwood
Journal:  Shock       Date:  2017-01       Impact factor: 3.454

9.  Active players in resolution of shock/sepsis induced indirect lung injury: immunomodulatory effects of Tregs and PD-1.

Authors:  Lunxian Tang; Jianwen Bai; Chun-Shiang Chung; Joanne Lomas-Neira; Yaping Chen; Xin Huang; Alfred Ayala
Journal:  J Leukoc Biol       Date:  2014-07-31       Impact factor: 4.962

10.  Frontline Science: Defects in immune function in patients with sepsis are associated with PD-1 or PD-L1 expression and can be restored by antibodies targeting PD-1 or PD-L1.

Authors:  Andriani C Patera; Anne M Drewry; Katherine Chang; Evan R Beiter; Dale Osborne; Richard S Hotchkiss
Journal:  J Leukoc Biol       Date:  2016-09-26       Impact factor: 4.962

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