The relationship between CD4+CD25+CD127- regulatory T cells and inflammatory response and outcome during shock states
© Hein et al.; licensee BioMed Central Ltd. 2010
Received: 23 September 2009
Accepted: 15 February 2010
Published: 15 February 2010
Although regulatory T lymphocytes (Tregs) have a pivotal role in preventing autoimmune diseases and limiting chronic inflammatory conditions, they may also block beneficial immune responses by preventing sterilizing immunity to certain pathogens.
To determine whether naturally occurring Treg cells have a role in inflammatory response and outcome during shock state we conducted an observational study in two adult ICUs from a university hospital. Within 12 hours of admission, peripheral whole blood was collected for the measurement of cytokines and determination of lymphocyte count. Sampling was repeated at day three, five and seven. Furthermore, an experimental septic shock was induced in adult Balb/c mice through caecal ligation and puncture.
Forty-three patients suffering from shock (26 septic, 17 non septic), and 7 healthy volunteers were included. The percentage of Tregs increased as early as 3 days after the onset of shock, while their absolute number remained lower than in healthy volunteers. A similar pattern of Tregs kinetics was found in infected and non infected patients. Though there was an inverse correlation between severity scores and Tregs percentage, the time course of Tregs was similar between survivors and non survivors. No relation between Tregs and cytokine concentration was found. In septic mice, although there was a rapid increase in Treg cells subset among splenocytes, antibody-induced depletion of Tregs before the onset of sepsis did not alter survival.
These data argue against a determinant role of Tregs in inflammatory response and outcome during shock states.
Despite this, our knowledge of the underlying process of sepsis is still unclear, and this is particularly obvious from an immunological standpoint. Indeed, after having considered for years the host response to severe infection only as a stormy inflammatory reaction, it appears now that anti-inflammatory components are released at the same time as pro-inflammatory mediators and the net result of these two arms of immune response determines the patient's phenotype: overwhelming inflammation with early death, delicate balance between pro- and anti-inflammation with progressive recovering, or exaggerated anti-inflammation predisposing to superinfections [3, 4].
The later phenotype has been called 'immune paralysis' or 'leukocyte reprogramming' and is characterized by a lymphocytes' anergy, apoptosis, and a reduced capacity to present antigens . Several mechanisms may partly explain this phenomenon such as an increased production of anti-inflammatory cytokines IL-10 and transforming growth factor (TGF)-β .
More recently, several groups have implicated an active lymphoid suppressor cell population: the naturally occurring regulatory T cells (Tregs) [5, 6]. Although these CD4+CD25+ cells make up only a small fraction of the T-lymphocyte population, they are potent inhibitors of immune response , and are now widely regarded as the primary mediators of peripheral tolerance, able to maintain immune homeostasis, to prevent autoimmunity, and to modulate inflammation induced by pathogens and environmental insults .
From a functional perspective, the suppressive mechanisms used by Tregs can be divided into four groups: suppression by inhibitory cytokines (such as IL-10 and TGF-β) and cell-to-cell contact, suppression by cytolysis through the secretion of granzymes, suppression by metabolic disruption, and suppression by the modulation of dendritic cells maturation or function (through cell-surface molecules such as cytotoxic T lymphocyte antigen-4, IL-10 and TGF-β) .
Although Tregs have a pivotal role in preventing autoimmune diseases and limiting chronic inflammatory disorders, they may also block beneficial immune responses by preventing sterilizing immunity to certain pathogens [3, 9]. As an elevated percentage of Tregs was observed during septic shock, a role of this cell subset has been suspected during this syndrome . Indeed, data are scarce and conflicting: whereas Heuer and colleagues demonstrated that adoptive transfer treatment with ex vivo-stimulated Tregs improved sepsis mortality , Scumpia and colleagues found that endogenous Tregs did not play a role in sepsis mortality in mice .
In humans, Venet and colleagues showed that, although the percentage of Tregs increased during sepsis, absolute cell count was decreased . Moreover, these authors recently found an inverse correlation between Tregs and lymphocyte proliferation capacity .
In the present study we report that the relative increase in Tregs appears lately during septic shock and show that this phenomenon is not specific to sepsis but also occurs during non-septic shock. We also observe that the percentage of Tregs is inversely correlated with severity at admission, although with no relation to cytokine plasma concentrations. Finally, we demonstrate that Tregs do not influence survival or cytokine production in a polymicrobial model of septic shock in mice.
Materials and methods
All consecutive patients newly admitted to the medical ICUs of two French teaching hospital between January 2007 and June 2007 were prospectively enrolled in the study if they were suffering from shock whatever its etiology. Septic shock was defined by the standard criteria of the American College of Chest Physicians/Society of Critical Care Medicine consensus conference , and non-septic shock states were defined according to definitions used by Antonelli and colleagues . Patients who were immunocompromised were not enrolled (treatment with corticosteroids > 0.5 mg/kg equivalent prednisolone, bone marrow or organ transplant recipients, leukopenia (white blood cell count < 1000/mm3) or neutropenia (polymorphonuclear granulocyte count < 500/mm3), hematological malignancy or AIDS). Patients who presented with early death or discharge (within 12 hours after admission) were also excluded. Seven healthy volunteers from the laboratory served as controls: four men, three women, mean age 37.5 ± 3.6 years, without chronic or acute diseases. Approvals from the Comité de Protection des Personnes-EST III and the ethical committee of the Société de Réanimation de Langue Française were obtained, and the informed consents of the patients and volunteers were sought prior to inclusion.
Upon admission to the ICU, the following data were recorded for each patient: age; sex; severity of underlying medical condition according to the criteria of McCabe and Jackson ; Simplified Acute Physiology Score (SAPS) II ; Sepsis-related Organ Failure Assessment (SOFA) score ; reason for admission into the ICU; principal diagnosis; vital signs; respiratory parameters; routine blood tests and microbiological culture results. Survival or death in the ICU was assessed during a follow-up period of up to 28 days.
Within 12 hours upon admission, peripheral whole blood was collected on citrated tubes. Sampling was repeated at day three, five and seven provided that the patient was still in the ICU.
Flow cytometry analyses were conducted on a Coulter Cytomics FC500 cytometer (Beckman-Coulter, Hialeah, FL, USA). All the monoclonal antibodies and the isotypic controls (except anti-Foxp3) used were from Immunotech (Marseille, France): PE-Texas Red (ECD)-labelled anti-CD3, fluorescein isothiocyanate (FITC)-labelled anti-CD14, phycoerythrin (PE)-labelled anti-HLA-DR (clone IM 1639), FITC-labelled anti-CD3, PC5-labeled anti-CD56, PC5-labelled anti-natural killer (NK) G2D, PC5-labeled anti-CD4, FITC-labelled anti-CD25 and PE-labelled anti-CD127; the Foxp3 monoclonal antibody was from eBiosciences (San Diego, CA, USA). After red blood cells lysis (Q-prep system, Beckman Coulter, Hialeah, FL, USA), naturally occurring Tregs were characterized by the expression of CD4 and CD25 and the lack of expression of CD127. We also characterized the number of monocytes and NK cells based upon the expression of the usual markers (CD45, CD14, HLA-DR, CD16, and NKG2D, respectively). Results are expressed as percentages of the CD4+ lymphocyte population and as number of cells per microliter of whole blood.
Cytokines plasma concentrations
Plasma concentrations of IL-2, IL-4, IL-5, IL-10, interferon (INF) γ and TNFα were quantified through fluorescence activated cell sorting (FACS) by the use of human Th1/Th2 CBA kit (BD Biosciences, San Diego, CA, USA) according to the recommendations of the manufacturer. Intra- and inter-assay coefficients of variation were less than 8%. Concentration of TGFβ was determined by ELISA (R&D Systems, Lille, France).
Polymicrobial sepsis in mice
All experiments were approved by the Institutional Animal Care and Use Committee. Adult (5 to 6 weeks, 20 to 23 g) male Balb/c mice were purchased from the Centre d'élevage Dépré (Saint-Doulchard, France).
For induction of polymicrobial sepsis, mice were anesthetized by intraperitoneal administration of ketamine and xylazine in 0.2 ml sterile pyrogen-free saline. The cecum was exposed through a 1.0 cm abdominal midline incision and subjected to ligation of the distal half followed by two punctures with a 21G needle. A small amount of stool was expelled from the punctures to ensure patency. The cecum was replaced into the peritoneal cavity and the abdominal incision closed in two layers. After surgery, all mice were injected subcutaneously with 0.5 ml of physiologic saline solution for fluid resuscitation and subcutaneously every 12 hours with 1.25 mg (i.e., 50 μg/g) of imipenem. A sham operation was performed by isolating the cecum without ligation or puncture.
When specified, animals were given either an intraperitoneal injection of 500 μg of affinity purified CD25 (PC61 hybridoma)-depleting antibody (BioExpress, West Lebanon, NH, USA) or an identical volume (250 μl) of sterile normal saline 72 hours before the caecal ligation and puncture (CLP). Administration of the antibody (250 μg) or normal saline was repeated two hours before the procedure.
Animals were observed for up to seven days to determine survival. For certain experiments, 4 to 6 mice were euthanized at 24, 48 or 96 hours after surgery to harvest blood or splenocytes. Among splenocytes, the Tregs were considered to be the CD4+CD25+Foxp3+ cells on FACS.
At indicated times, plasma concentrations of TNF-α, IL-1β and IL-6 were measured by ELISA.
Changes in time or between groups were analyzed by one-way analysis of variance. Comparisons between patients with septic shock, patients with non-septic shock and/or healthy volunteers were performed by using Student's t test as normally distributed values (Kolmogoroff-Smirnov test), Mann-Whitney U test, or Kruskal Wallis test when indicated. Data are expressed as mean ± standard deviation or median ± interquartile range when appropriate. Correlations were established using Spearman's test. Survival analysis (mice) was performed using the log rank test after drawing the Kaplan Meier survival curves. Analysis was completed with the Statview software (Abacus Concepts, Berkeley, CA, USA), with a two-tailed P value less than 0.05 considered as statistically significant.
Characteristics of the studied population
Septic shock patients (n = 26)
Non-septic shock patients (n = 17)
McCabe and Jackson criteria
SAPS II score
Mean arterial pressure, mmHg
Arterial lactate (mmol/L)
C-reactive protein, mg/L
The septic shock patients had lower neutrophils and lymphocytes counts, higher plasma concentrations of C-reactive protein and procalcitonin as compared with non-septic patients.
Kinetics of Tregs
The sub-populations of lymphocytes on admission
(n = 26)
Non septic shock
(n = 17)
(n = 7)
CD4+ lymphocytes (cells/μL)*
Tregs (% of CD4+)
NK cells (cells/μL)†
NK cells (% of lymphocytes)
By day three, both Treg numbers and percentages progressively increased in both groups of patients, especially the septic ones, although there was no statistical difference between the two groups of patients (Figures 1b and 1c). At day seven, although the percentage of Tregs was higher in the septic patients than in the non-septic patients and healthy volunteers, there were no differences in terms of absolute count, reflecting the persistence of the CD4+ lymphopenia in the septic shock group.
Correlation between Tregs, severity and cytokines plasma concentrations
By contrast, we were unable to find any correlation between Tregs and plasma cytokine (IL-2, IL-4, IL-5, IL-10, INFγ, TNFα and TGF-β) concentrations, either taken individually or expressed as Th1/Th2 ratios (data not shown). This absence of correlation was found in septic as well as non-septic patients.
NK cells kinetics
NK cells have been advocated as an important component influencing outcome during septic shock .
Polymicrobial sepsis in mice
Finally, plasma concentrations of TNF-α (Figure 8), IL-1β or IL-6 (not shown) were not different between the two groups of mice.
There is now enough evidence that morbidity and mortality occurring during septic, as well as non-septic, shock may be due to the effect of distinct mechanisms over time: in addition to an overwhelming pro-inflammatory immune response, concomitant counter-inflammatory mechanisms develop that may be responsible for 'immune paralysis' . Although naturally occurring Tregs have been found to play major roles in a wide range of disorders, such as tumour progression, inflammation or transplantation tolerance [4, 7, 9], their implication during shock states is unclear.
In agreement with the findings of Monneret and colleagues [10, 19], we observed that the percentage of Tregs increased as early as three days after the onset of shock, while their absolute number remained lower than in healthy volunteers. This phenomenon has been explained by Venet and colleagues by a decrease of the CD4+CD25- lymphocytes subset , most probably through apoptosis. Adding to the similarities that exist between septic and non-septic shock in terms of immune derangement, we found similar patterns of Treg kinetics in infected and non-infected patients. Indeed, immune paralysis is also observed during trauma/haemorrhage or cardiogenic shock as demonstrated by a reduced ability of antigen presentation or ex vivo pro-inflammatory cytokine production . Nevertheless, this apparent absence of difference between septic and non-septic patients may also, at least in part, be explained by the small sample size and the variability in each of the measurements.
Although we observed an inverse correlation between severity, assessed by SOFA score or arterial lactate concentration, and percentage of Tregs, the time course of the percentage or absolute number of Tregs was similar between survivors and non-survivors. Most probably, this finding may also be explained by the negative correlation between severity and CD4+CD25- lymphocyte number (data not shown). Nevertheless, only considering the group of septic shock patients, we observed that survivors had higher percentage and absolute numbers of Tregs by day five than non-survivors. Although this finding may suggest a specific effect of Tregs in sepsis outcome, the low number of non-survivors studied at days five and seven preclude any definite conclusion.
The influence of cytokines on Treg proliferation or activation is unknown during shock states, as is the effect of Tregs on cytokine production. Here we were unable to show any correlation between percentage or absolute count of Tregs and plasma cytokine concentration (IL-2, IL-4, IL-5, IL-10, INFγ, TNFα and TGF-β), taken individually or expressed as a Th1/Th2 balance. Therefore, Tregs do not seem to modulate the inflammatory response during shock in vivo. Of note, this absence of relation was found in septic as well as in non-septic patients.
As NK cells have recently been advocated to play a role in sepsis outcome, we also investigated the kinetics of this cell's subset. In contrast to the findings of Giamarellos-Bourboulis and colleagues , we observed that the percentage of NK cells was not different between patients and healthy volunteers throughout the study period. This discrepancy may be explained by the unexpectedly low NK percentage (4.12%) found in the six healthy volunteers, and the old age of the patients (77 years) enrolled in the Greek study. Patients with shock presented with a constantly decreased NK absolute count, without any differences between septic and non-septic shock. Finally, NK cell kinetics was similar between survivors and non-survivors. Taken together, these data suggest a marginal role of NK cells on shock outcome, although the relatively small number of patients enrolled precludes definite conclusion.
To further evaluate the role of Tregs on sepsis outcome, we used a well characterized CLP model of polymicrobial sepsis in mice. In accordance with Scumpia and colleagues , we observed a rapid increase in Tregs subset among splenocytes in septic animals. However, despite their increased proportion, antibody-induced depletion of Tregs before the onset of sepsis did not alter survival. Again, these data are in line with those of Scumpia and colleagues . The originality of the present study stems from the septic shock model we used: mice were fluid resuscitated and antibiotics given, further approaching the complex physiopathology of human sepsis. Therefore, our data are more able to be extrapolated to human septic shock. In accordance with what we observed in humans, Tregs did not appear to influence cytokine production (TNF-α, IL-1β, IL-6) in septic animals.
In contrast, our animal data seem in discordance with those reported by Heuer and colleagues . Several important differences between these two studies need to be underlined. First, Heuer and colleagues performed an adoptive transfer of in vitro prestimulated Tregs and then it is not clear whether the protective role on survival was due to Tregs themselves or to the artificial induction of membrane/soluble mediators. Second, the model of CLP we used here appears to be more stringent and thus, a potential protective role of Tregs may have been masked by the severity of the model. Finally, although we used the classical and well-accepted anti-CD25 antibody approach to deplete Tregs, we must acknowledge that anti-CD25 is not specific for Tregs and leads to the depletion of other important cells (activated T cells). Moreover, anti-CD25 antibody may not have completely eliminated CD25low Tregs.
Taken together, these data argue against a determinant role of naturally occurring Tregs on inflammatory response and outcome during shock states.
Percentage of Tregs increases early after the onset of shock whatever its etiology, while their absolute number remains lower than in healthy volunteers.
Percentage of Tregs is inversely correlated to severity of shock, although the time course of percentage or absolute number of Tregs is similar between survivors and non-survivors.
There is no correlation between percentage or absolute number of Tregs and plasma cytokine concentrations taken individually or expressed as a Th1/Th2 balance.
In a mouse model of septic shock, antibody-induced depletion of Tregs before the onset of sepsis does not alter survival.
enzyme-linked immunosorbent assay
fluorescent activated cell sorting
Simplified Acute Physiology Score
Sepsis-related Organ Failure Assessment
transforming growth factor
tumor necrosis factor
regulatory T cells.
This work has been supported by a Contrat de Programme Recherche Clinique (CPRC) 2007 from Nancy University's hospital.
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