Evidence for Persistent Immune Suppression in Patients Who Develop Chronic Critical Illness After Sepsis

Many sepsis survivors develop chronic critical illness (CCI) and are assumed to be immunosuppressed, but there is limited clinical evidence to support this. We sought to determine whether the incidence of secondary infections and immunosuppressive biomarker profiles of patients with CCI differ from...

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Veröffentlicht in:Shock (Augusta, Ga.) Ga.), 2018-03, Vol.49 (3), p.249-258
Hauptverfasser: Stortz, Julie A, Murphy, Tyler J, Raymond, Steven L, Mira, Juan C, Ungaro, Ricardo, Dirain, Marvin L, Nacionales, Dina C, Loftus, Tyler J, Wang, Zhongkai, Ozrazgat-Baslanti, Tezcan, Ghita, Gabriela L, Brumback, Babette A, Mohr, Alicia M, Bihorac, Azra, Efron, Philip A, Moldawer, Lyle L, Moore, Frederick A, Brakenridge, Scott C
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container_end_page 258
container_issue 3
container_start_page 249
container_title Shock (Augusta, Ga.)
container_volume 49
creator Stortz, Julie A
Murphy, Tyler J
Raymond, Steven L
Mira, Juan C
Ungaro, Ricardo
Dirain, Marvin L
Nacionales, Dina C
Loftus, Tyler J
Wang, Zhongkai
Ozrazgat-Baslanti, Tezcan
Ghita, Gabriela L
Brumback, Babette A
Mohr, Alicia M
Bihorac, Azra
Efron, Philip A
Moldawer, Lyle L
Moore, Frederick A
Brakenridge, Scott C
description Many sepsis survivors develop chronic critical illness (CCI) and are assumed to be immunosuppressed, but there is limited clinical evidence to support this. We sought to determine whether the incidence of secondary infections and immunosuppressive biomarker profiles of patients with CCI differ from those with rapid recovery (RAP) after sepsis. This prospective observational study evaluated 88 critically ill patients with sepsis and 20 healthy controls. Cohorts were defined based on clinical trajectory (early death, RAP, or CCI), whereas immunosuppression was clinically determined by the presence of a postsepsis secondary infection. Serial blood samples were collected for absolute lymphocyte counts (ALCs), monocytic human leukocyte antigen-DR (mHLA-DR) expression, and plasma-soluble programmed death-ligand 1 (sPD-L1) concentrations. Of the 88 patients with sepsis, 3 (3%) died within 14 days of sepsis onset, 50 (57%) experienced RAP, and 35 (40%) developed CCI. Compared with RAP patients, CCI patients exhibited a higher incidence and overall number of infections adjusted for hospital length of stay. ALC and mHLA-DR levels were dramatically reduced at the time of sepsis diagnosis when compared with healthy controls, whereas sPD-L1 concentrations were significantly elevated. There were no differences between RAP and CCI patients in ALC, sPD-L1, or mHLA-DR at the time of diagnosis or within 24 h after sepsis diagnosis. However, in contrast to the RAP group, CCI patients failed to exhibit any trend toward restoration of normal values of ALC, HLA-DR, and sPD-L1. Septic patients demonstrate clinical and biological evidence to suggest they are immunosuppressed at the time of sepsis diagnosis. Those who develop CCI have a greater incidence of secondary infections and persistently aberrant markers of impaired host immunity, although measurements at the time of sepsis onset did not distinguish between subjects with RAP and CCI.
doi_str_mv 10.1097/SHK.0000000000000981
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We sought to determine whether the incidence of secondary infections and immunosuppressive biomarker profiles of patients with CCI differ from those with rapid recovery (RAP) after sepsis. This prospective observational study evaluated 88 critically ill patients with sepsis and 20 healthy controls. Cohorts were defined based on clinical trajectory (early death, RAP, or CCI), whereas immunosuppression was clinically determined by the presence of a postsepsis secondary infection. Serial blood samples were collected for absolute lymphocyte counts (ALCs), monocytic human leukocyte antigen-DR (mHLA-DR) expression, and plasma-soluble programmed death-ligand 1 (sPD-L1) concentrations. Of the 88 patients with sepsis, 3 (3%) died within 14 days of sepsis onset, 50 (57%) experienced RAP, and 35 (40%) developed CCI. Compared with RAP patients, CCI patients exhibited a higher incidence and overall number of infections adjusted for hospital length of stay. ALC and mHLA-DR levels were dramatically reduced at the time of sepsis diagnosis when compared with healthy controls, whereas sPD-L1 concentrations were significantly elevated. There were no differences between RAP and CCI patients in ALC, sPD-L1, or mHLA-DR at the time of diagnosis or within 24 h after sepsis diagnosis. However, in contrast to the RAP group, CCI patients failed to exhibit any trend toward restoration of normal values of ALC, HLA-DR, and sPD-L1. Septic patients demonstrate clinical and biological evidence to suggest they are immunosuppressed at the time of sepsis diagnosis. 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subjects Adult
Aged
B7-H1 Antigen - blood
B7-H1 Antigen - immunology
Critical Illness
Female
HLA-DR Antigens - blood
HLA-DR Antigens - immunology
Humans
Immune Tolerance
Lymphocyte Count
Male
Middle Aged
Prospective Studies
Sepsis - blood
Sepsis - immunology
title Evidence for Persistent Immune Suppression in Patients Who Develop Chronic Critical Illness After Sepsis
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