Abstract
Background
Sepsis is a prominent reason for intensive care unit (ICU) admission in patients with HIV. We aimed to investigate the impact of HIV infection on presentation, outcome and host response in sepsis.
Methods
We performed a prospective observational study in the ICUs of two tertiary hospitals. For the current analyses, we selected all patients diagnosed with sepsis within 24 hours after admission. Host response biomarkers were analyzed in a more homogeneous subgroup of admissions involving HIV-positive patients with pneumosepsis, matched to admissions of HIV-negative patients for age, gender and race. Matching was done by nearest neighbor matching with R package “MatchIt”.
Results
We analyzed 2251 sepsis admissions including 41 (1.8 %) with HIV infection (32 unique patients). HIV-positive patients were younger and admission of HIV-positive patients more frequently involved pneumonia (73.2 % versus 48.8 % of admissions of HIV-negative patients, P = 0.004). Disease severity and mortality up to one year after admission did not differ according to HIV status. Furthermore, sequential plasma levels of host response biomarkers, providing insight into activation of the cytokine network, the vascular endothelium and the coagulation system, were largely similar in matched admissions of HIV-positive and HIV-negative patients with pneumosepsis.
Conclusions
Sepsis is more often caused by pneumonia in HIV-positive patients. HIV infection has little impact on the disease severity, mortality and host response during sepsis.
Electronic supplementary material
The online version of this article (doi:10.1186/s13054-016-1469-0) contains supplementary material, which is available to authorized users.
Keywords: HIV, Sepsis, Pneumonia, Intensive care units
Background
The spectrum of disease in human immunodeficiency virus (HIV)-infected patients has changed dramatically since the introduction of combination antiretroviral therapy (cART) [1]. The incidence of opportunistic infections has decreased and long-term survival has improved to an extent that HIV infection has become a chronic disease [1]. However, invasive bacterial infections and sepsis remain an important cause of morbidity and mortality in patients with HIV [2, 3], and previous studies have demonstrated the importance of sepsis as a reason for intensive care unit (ICU) admission [3–8]. Advanced HIV infection has been associated with higher mortality in patients with sepsis compared to mortality in HIV-negative patients with sepsis [9–11].
Sepsis is characterized by an imbalanced host response, characterized amongst other factors by release of proinflammatory and anti-inflammatory cytokines, activation of the vascular endothelium and stimulation of the coagulation system with concurrent impairment of anticoagulant mechanisms [12]. HIV infection is associated with activation and deregulation of several cellular and mediator pathways also implicated in the pathogenesis of sepsis, which has led to the hypothesis that HIV infection may further disturb the host response in sepsis [13]. However, few studies have investigated the immune response to sepsis in patients with HIV co-infection.
We aimed to compare the presentation and outcome of sepsis in the presence or absence of HIV co-infection in an area with widely available cART. In addition, in a more homogeneous subgroup of patients with pneumosepsis, we sought to obtain insight into the influence of HIV co-infection on the host response.
Methods
Study design, patients and definitions
This study was conducted as part of the Molecular Diagnosis and Risk Stratification of Sepsis (MARS) project, a prospective observational study in the ICUs of two tertiary teaching hospitals (Academic Medical Center in Amsterdam and University Medical Center Utrecht, The Netherlands) [14]. Trained ICU researchers prospectively collected demographic, clinical, microbiological and interventional data [14]. In the MARS study, assignment of pathogens to pneumonia cases was based on post hoc physician assessment, using all available information, including pathogens cultured from blood, lower respiratory tract samples and respiratory secretions and serology and PCR results, combined with the clinical decision to treat the patient for the particular causative pathogen, in multidisciplinary meetings.
Information on CD4 counts, viral loads and cART was collected from patient files. CD4 counts and viral loads measured between 120 days prior to and 30 days after admission were considered representative. If multiple samples were available, the first sample was included in our analyses. Organ failure was defined by a score of 3 or greater on the Sequential Organ Failure Assessment (SOFA) score, or a score of 1 or more for cardiovascular failure [15]. Shock was defined by the use of vasopressors (noradrenaline) for hypotension in a dose of 0.1 mcg/kg/min during at least 50 % of the ICU day. The plausibility of infection was assessed post hoc and classified on a 4-point scale (none, possible, probable or definite) according to Center for Disease Control and Prevention [16] and International Sepsis Forum consensus definitions [14, 17].
For the current analysis we selected all patients admitted to the ICU between January 2011 and July 2013 with sepsis diagnosed within 24 hours after ICU admission, defined as the presence of infection combined with at least one additional parameter as described in the 2001 International Sepsis Definitions Conference [18]. Patients with a post hoc infection likelihood of “none” were excluded, as were patients transferred from another ICU, except for those referred to one of the study centers on the day of admission. The Municipal Personal Records Database was consulted to determine survival up to one year after ICU admission. In The Netherlands, all deaths are immediately reported to this database, so this provides a reliable and up-to-date means to assess mortality. If a patient had multiple admissions, only the first admission was used to assess mortality.
Biomarker measurements
Daily (at admission and at 6 a.m. thereafter) left-over plasma (obtained from blood drawn for routine patient monitoring) was stored within 4 hours at -80 °C. All measurements were done in EDTA anticoagulated plasma obtained on admission (day 0) and days 2 and 4. Tumor necrosis factor alpha (TNF-α), interleukin-1beta (IL-1β), interferon-gamma (IFN-γ), IL-6, IL-8, IL-10, IL-13, soluble intercellular adhesion molecule-1 (ICAM-1) and soluble E-selectin were measured using FlexSet cytometric bead arrays (BD Bioscience, San Jose, CA, USA) using FACS Calibur (Becton Dickenson, Franklin Lakes, NJ, USA). Angiopoietin-1, angiopoietin-2, protein C, antithrombin (R&D systems, Abingdon, UK), and D-dimer (Procartaplex, eBioscience, San Diego, CA, USA) were measured by Luminex multiplex assay using BioPlex 200 (BioRad, Hercules, CA, USA). Normal biomarker values were acquired from EDTA plasma from 27 age-matched and gender-matched healthy volunteers, from whom written informed consent was obtained.
Statistical analysis
Data-analyses were performed in R (v3.1.1) [19]. Baseline characteristics of study groups were compared using the chi-square test for categorical variables and the t test or Wilcoxon rank sum test for continuous variables. In order to adjust for differences in clinical characteristics between groups, each HIV patient with pneumonia was matched by age, gender and race (white) to three HIV-negative controls, using nearest neighbor matching with R package “MatchIt”. Biomarkers were transformed to a log scale and mixed models were used to analyze repeated measurements. P values below 0.05 were considered statistically significant.
Results
Study population
A total of 6994 admissions, involving 5920 unique patients, were included during the study period, including 58 admissions of HIV-positive patients (0.8 %). We excluded 325 admissions because the patients had been transferred from other ICUs. Of the remaining 6669 admissions, 2251 (1889 patients) had a sepsis diagnosis in the first 24 hours of ICU admission, including 41 admissions (1.8 %) of 32 unique patients (1.7 %) with HIV infection (Table 1). The other 17 HIV-positive admissions (16 unique patients) during this study period were for non-infectious reasons, predominantly postoperative surveillance (n = 4), respiratory insufficiency (n = 3) and pulmonary embolism (n = 2).
Table 1.
Baseline characteristics and outcome of all sepsis admissions stratified according to HIV infection status
| HIV-positive (n = 41) | HIV-negative (n = 2210) | P | |
|---|---|---|---|
| Demographicsa | |||
| Age, years, mean (SD) | 49.6 (12) | 60.4 (15.5) | <0.0001 |
| Gender, male (%) | 24 (75) | 1154 (6) | 0.14 |
| Race, white (%) | 18 (56.2) | 1652 (89) | 0.005 |
| Admissions | |||
| Readmission (%) | 9 (22.0) | 353 (16.0) | 0.39 |
| New HIV diagnosis (%) | 6 (14.6) | -- | -- |
| Severity of disease in first 24 hours | |||
| SOFA score, median (IQR)b | 7 (3-10.5) | 7 (4–9) | 0.38 |
| Organ failure (%) | 35 (85.4) | 1802 (81.5) | 1 |
| Shock (%) | 9 (22) | 606 (27.4) | 0.50 |
| HIV disease severity and treatment | |||
| CD4 count, cells/mm3, median (IQR)c | 70 (23-346) | -- | -- |
| Viral load, cp/ml, median (IQR)d | 105 (48-54916) | -- | -- |
| On cART (%) | 29 (70.7) | -- | -- |
| Viral suppression (%) | 18 (47.4) | -- | -- |
| Outcome | |||
| Length of ICU stay, median days (IQR) | 4 (1–11) | 4 (2–8) | 0.47 |
| Organ failure during admission (%) | 37 (90.2) | 1915 (86.7) | 0.73 |
| Shock during admission (%) | 15 (36.6) | 750 (33.9) | 0.74 |
| 30-day mortality (%)a | 6 (18.8) | 481 (25.9) | 0.42 |
| 60-day mortality (%)a | 11 (34.4) | 568 (30.6) | 0.72 |
| 90-day mortality (%)a | 13 (40.6) | 629 (33.9) | 0.57 |
| 1-year mortality (%)a | 16 (50) | 794 (42.8) | 0.35 |
aDemographic and mortality data are given for the first ICU admission during the study period; readmissions were not included, resulting in analysis of 32 HIV-positive patients and 1857 HIV-negative patients. From the total of 2251 admissions, 23 were lost to follow up at day 30 (1 %), 32 at day 60 (1.4 %), 37 at day 90 (1.6 %), and 59 at 1 year (2.6 %) after ICU admission. bThe central nervous system score was excluded from the Sequential Organ Failure Assessment (SOFA) score calculation, because of a large number of sedated patients. cCD4 counts were available for 39 admissions. In 32 patients (82 %) the CD4 count was obtained within 120 days prior to admission, and 7 patients (18 %) had a CD4 count obtained on admission or within 30 days after admission. dViral loads were available for 39 admissions. Viral suppression was defined as a viral load below the detection limit, which was <40 copies/ml or <50 copies/ml, depending on the hospital laboratory. cART combination antiretroviral therapy, IQR interquartile range, SD standard deviation
Presentation, cause and outcome of sepsis
Sepsis admissions with HIV co-infection involved younger patients, who were less likely to be Caucasian, compared to sepsis admissions without HIV infection (Table 1). The majority of HIV-positive patient admissions (n = 29, 70.7 %) involved patients who were on cART, but only 18 (47.4 %) had complete viral suppression (HIV load <50 copies/ml). There were 6 admissions (14.6 %) involving patients presenting with newly diagnosed HIV infection and the majority of HIV admissions presented with overt immune suppression (CD4 counts <200 cells/mm3 in 56.1 % and <350 cells/mm3 in 73.2 % of admissions). Pneumonia was the most common infection in both HIV-positive and HIV-negative admissions, but pneumonia was more frequent in HIV-positive patient admissions (n = 30 (73.2 %) versus 1048 (48.8 %) in admissions involving patients with sepsis who were HIV-negative, P = 0.004) (Fig. 1). The proportion of patients admitted with organ failure or shock was similar in HIV-positive and HIV-negative patients (Table 1). Likewise, the occurrence of organ failure and shock at any day during ICU stay was similar between groups. Crude mortality up to one year after ICU admission did not differ between HIV-positive and HIV-negative patients with sepsis.
Fig. 1.
Primary sites of infection in patients with sepsis admitted to the ICU stratified by HIV status. Numbers in the figure represent the numbers of patients per group. P values are indicated for differences between HIV-positive and HIV-negative patients at each time point
Presentation, cause and outcome of pneumonia
Considering the strong predominance of pneumonia amongst HIV-positive admissions, we focused our further analyses on 30 admissions of HIV-positive patients with pneumosepsis (Table 2). Considering the large demographic differences according to HIV status, we composed a control cohort of 90 admissions of HIV-negative patients with pneumonia, matched for age, sex and race. In the matched cohort demographic characteristics were similar between groups. The matched cohort contained more HIV-positive than HIV-negative patients who were readmitted. In order to explore reasons for the relatively high readmission rates amongst HIV-positive patients we compared HIV-positive admissions with and without readmission (Additional file 1); this analysis did not provide a clear explanation. Although the severity of disease was comparable between HIV-positive and HIV-negative admissions, as reflected by the SOFA score and the percentage of patients presenting with organ failure or shock, HIV-positive pneumosepsis admissions were significantly less likely to require mechanical ventilation in the first 24 hours. Causative pathogens in patients with pneumosepsis are outlined in Table 3. The most common pathogens in HIV-positive admissions were Streptococcus pneumoniae, Staphylococcus aureus and Pneumocystis jirovecii. While S. pneumoniae and S. aureus were similarly frequent in HIV-negative patients, P. jirovecii was more common in HIV-positive patients compared with unmatched HIV-negative patients with pneumosepsis, but not when compared to matched HIV-negative patients with pneumosepsis. In the latter group P. jirovecii pneumonia occurred in patients on immunosuppressive therapy. Cytomegalovirus (CMV) was a more frequent pathogen in HIV-positive admissions, both in unmatched and matched analyses. Crude mortality up to one year after ICU admission did not differ between HIV-positive and HIV-negative patients with pneumonia (either unmatched or matched) (Table 2).
Table 2.
Baseline characteristics and outcome of unmatched and matched admissions for pneumonia stratified by HIV status
| Unmatched patients | Matched patientsa | ||||
|---|---|---|---|---|---|
| HIV-positive (n = 30) | HIV-negative (n = 1078) | P | HIV-negative (n = 90) | P | |
| Demographicsb | |||||
| Age, years, mean (SD) | 51.5 (11.1) | 60.6 (16.2) | 0.001 | 50.8 (12.9) | 0.83 |
| Gender, male (%) | 17 (77.3) | 604 (64.9) | 0.28 | 69 (84.1) | 0.52 |
| Race: white (%) | 14 (63.6) | 831 (89.3) | 0.002 | 67 (81.7) | 0.10 |
| Comorbiditiesb | |||||
| Chronic renal insufficiency (%) | 2 (9.1) | 101 (10.8) | 1 | 11 (13.4) | 0.75 |
| COPD (%) | 4 (18.2) | 178 (19.1) | 1 | 11 (13.4) | 0.73 |
| Diabetes mellitus (%) | 3 (13.6) | 173 (18.6) | 0.59 | 14 (17.1) | 0.76 |
| Hematologic malignancy (%) | 5 (22.7) | 73 (7.8) | 0.03 | 10 (12.2) | 0.30 |
| Hypertension (%) | 8 (36.4) | 277 (29.8) | 0.63 | 14 (17.1) | 0.08 |
| Liver cirrhosis (%) | 1 (4.5) | 16 (1.7) | 0.32 | 2 (2.4) | 1 |
| Metastatic malignancy (%) | 2 (9.1) | 28 (3) | 0.16 | 2 (2.4) | 0.20 |
| Non-metastatic malignancy (%) | 2 (9.1) | 96 (10.3) | 1 | 5 (6.1) | 0.64 |
| Admissions | |||||
| Readmission (%) | 8 (26.7) | 147 (13.6) | 0.06 | 8 (8.9) | 0.03 |
| Community-acquired pneumonia (%) | 18 (60) | 565 (52.4) | 0.44 | 56 (62.2) | 1 |
| Severity of disease in first 24 hours | |||||
| SOFA score, median (IQR) | 6 (4–8) | 7 (3–10) | 0.30 | 7 (4-9) | 0.89 |
| Organ failure (%) | 884 (82) | 25 (83.3) | 1 | 81 (90) | 0.70 |
| Shock (%) | 262 (24.3) | 8 (26.7) | 0.84 | 35 (38.9) | 0.53 |
| Supportive care in the first 24 hours | |||||
| Mechanical ventilation (%) | 20 (66.7) | 859 (79.7) | 0.12 | 81 (90) | 0.006 |
| Renal replacement therapy (%) | 2 (6.7) | 69 (6.4) | 1 | 8 (8.9) | 1 |
| Outcome | |||||
| Length of stay ICU, median days (IQR) | 5 (1-15) | 4 (2-9) | 0.70 | 6 (3-11) | 0.33 |
| Organ failure during admission (%) | 27 (90) | 951 (88.2) | 1 | 87 (96.7) | 0.26 |
| Shock during admission (%) | 14 (46.7) | 340 (31.5) | 0.10 | 35 (38.9) | 0.53 |
| 30-day mortality (%)b | 4 (18.2) | 244 (26.2) | 0.47 | 19 (23.2) | 0.79 |
| 60-day mortality (%)b | 8 (36.4) | 290 (31.1) | 0.67 | 22 (26.8) | 0.43 |
| 90-day mortality (%)b | 9 (40.9) | 319 (34.3) | 0.66 | 22 (26.8) | 0.30 |
| 1-year mortality (%)b | 11 (50) | 412 (44.3) | 0.66 | 25 (30.5) | 0.12 |
Results are presented as number (%) unless stated otherwise. aPatients were matched for age, gender and race and compared with HIV-positive patients. bDemographics and mortality data are given for the first ICU admission during the study period; readmissions were not included, resulting in analysis from 22 HIV-positive patients, 931 HIV-negative unmatched and 82 HIV-negative matched patients. cART combination antiretroviral therapy, COPD chronic obstructive pulmonary disease, ICU intensive care unit, IQR interquartile range, SD standard deviation, SOFA Sequential Organ Failure Assessment
Table 3.
Causative pathogens in all unmatched and matched patients with pneumonia stratified according to HIV status
| Unmatched patients | Matched patients | ||||
|---|---|---|---|---|---|
| HIV-positive (n = 30) | HIV-negative (n = 1078) | P | HIV-negative (n = 90) | P | |
| Gram-positive bacteria (%) | 8 (26.7) | 216 (20) | 0.52 | 18 (20.0) | 0.44 |
| Streptococcus pneumoniae (%) | 4 (13.3) | 71 (6.6) | 0.27 | 5 (5.6) | 0.22 |
| Streptococcus species (%) | 0 | 19 (1.8) | 0.67 | 3 (3.3) | 0.56 |
| Staphylococcus aureus (%) | 4 (13.3) | 99 (9.2) | 0.52 | 6 (6.7) | 0.27 |
| Other Gram-positive bacteria (%) | 0 | 27 (2.5) | 0.62 | 4 (4.4) | 0.58 |
| Gram-negative bacteria (%) | 3 (10.0) | 349 (32.4) | 0.0075 | 36 (40.0) | 0.011 |
| Haemophilus influenzae (%) | 0 | 70 (6.5) | 0.26 | 9 (10) | 0.11 |
| Escherichia coli (%) | 1 (3.3) | 65 (6) | 0.71 | 5 (5.6) | 1 |
| Pseudomonas aeruginosa (%) | 0 | 64 (5.9) | 0.25 | 6 (6.7) | 0.33 |
| Klebsiella pneumoniae (%) | 1 (3.3) | 29 (2.7) | 1 | 3 (3.3) | 1 |
| Enterobacter cloacae (%) | 0 | 25 (2.3) | 0.63 | 1 (1.1) | 1 |
| Stenotrophomonas maltophilia (%) | 1 (3.3) | 11 (1) | 0.28 | 1 (1.1) | 0.44 |
| Other Gram-negative bacteria (%) | 0 | 85 (7.9) | 0.18 | 11 (12.2) | 0.06 |
| Yeast/fungi (%) | 6 (20.0) | 84 (7.8) | 0.036 | 18 (20.0) | 1 |
| Aspergillus species (%) | 1 (3.3) | 40 (3.7) | 1 | 9 (10) | 0.44 |
| Pneumocystis jirovecii (%) | 4 (13.3) | 15 (1.4) | 0.004 | 5 (5.6) | 0.22 |
| Other yeasts or fungi (%) | 1 (3.3) | 29 (2.7) | 1 | 4 (4.4) | 1 |
| Viruses (%) | 3 (10.0) | 70 (6.5) | 0.72 | 10 (11.1) | 1 |
| Influenza (%) | 0 | 38 (3.5) | 0.41 | 8 (8.9) | 0.19 |
| Cytomegalovirus (%) | 2 (6.7) | 5 (0.5) | 0.019 | 0 | 0.049 |
| Other viruses (%) | 1 (3.3) | 27 (2.5) | 1 | 2 (2.2) | 1 |
| Atypical mycobacteria (%) | 1 (3.3) a | 1 (0.1) b | 0.053 | 0 | 0.24 |
| Unknown (%) | 15 (50) | 500 (46.4) | 1 | 30 (33.3) | 0.10 |
Results are presented as number (%). Percentages represent the proportion of pneumonia cases caused by the particular pathogen. Multiple causative pathogens were isolated in some patients with pneumonia. a Mycobacterium avium. b Mycobacterium xenopi
Host response biomarkers in pneumosepsis
To obtain insight into the influence of HIV infection on the host response to sepsis we measured 14 biomarkers indicative of activation and/or deregulation of key pathways implicated in sepsis pathogenesis in 30 HIV-positive and 90 matched HIV-negative pneumosepsis admissions. As expected [20, 21], patients with sepsis displayed activation of the cytokine network (Fig. 2), the vascular endothelium (Fig. 3) and the coagulation system (Fig. 4). The concentrations of most host response biomarkers were similar in HIV-positive and HIV-negative admissions, except for IFN-γ and soluble ICAM-1, which were higher in HIV-positive admissions at days 0 and 2. These differences were no longer statistically significant when readmissions were excluded, thus analyzing only the first admission of unique patients (Additional file 2). The plasma concentrations of TNF-α, IL-1β and IL-13 were undetectable in the majority of patients and were not different between groups (data not shown).
Fig. 2.
Cytokine levels in matched patients with pneumonia stratified according to HIV infection status. Plasma cytokine levels on days 0, 2 and 4 after intensive care unit admission. Data in box-and-whisker diagrams depict the median and lower quartile, upper quartile and respective 1.5 IQR as whiskers (as specified by Tukey). Dashed lines represent median in 27 healthy volunteers. P values are indicated for differences between HIV-positive and HIV negative-patients at each time point. IFN interferon, IL interleukin
Fig. 3.
Endothelial cell activation markers in matched patients with pneumonia stratified according to HIV infection status. Plasma levels of soluble E-selectin, soluble intercellular adhesion molecule-1 (ICAM-1), angiopoietin-1 and angiopoietin-2 on days 0, 2 and 4 after intensive care unit admission. Data in box-and-whisker diagrams depict the median and lower quartile, upper quartile and the respective 1.5 IQR as whiskers (as specified by Tukey). Dashed lines represent median levels in 27 healthy volunteers. P values are indicated for differences between HIV-positive and HIV-negative patients at each time point
Fig. 4.
Coagulation activation markers in matched patients with pneumonia stratified according to HIV infection status. Plasma levels of D-dimer, protein C and antithrombin on days 0, 2 and 4 after intensive care unit admission. Data in box-and-whisker diagrams depict the median and lower quartile, upper quartile and the respective 1.5 IQR as whiskers (as specified by Tukey). Dashed lines represent median levels in 27 healthy volunteers. P values are indicated for differences between HIV-positive and HIV-negative patients at each time point
Discussion
We studied the impact of HIV infection on the presentation and outcome of sepsis, and particularly pneumosepsis. Our main findings were that disease severity and outcome are remarkably alike in HIV-positive and HIV-negative patients. In addition, plasma concentrations of biomarkers indicative of key host responses to sepsis were largely similar in HIV-positive and HIV-negative patients with pneumosepsis.
In previous studies, HIV/AIDS was independently associated with in-hospital mortality in ICU patients with sepsis [9–11]. These studies differ from the present investigation in patient selection [9, 10] and setting [11], which resulted in the inclusion of patients with more severe disease [9–11]. Standards of care for HIV patients have improved considerably over time and previous studies indicate that survival of critically ill HIV-infected patients continues to improve in the era of widespread availability of cART [22, 23]. Taken together these data suggest that access to care (e.g. cART and well-equipped ICUs) is an important factor in the outcome of sepsis in patients with HIV.
Pneumonia was a more frequent presentation in patients with sepsis and HIV co-infection. Previously, pneumonia was shown to be a major source of morbidity in HIV, even in patients with high CD4 cell counts [24]. Prior to the wide availability of cART, P jirovecii pneumonia was a common reason for ICU admission [25, 26]. In our cohort P. jirovecii was a more common pathogen in HIV-positive patients, in addition to CMV, but the numbers of these opportunistic pathogens were relatively small, with the majority of pneumonia cases being caused by bacterial pathogens, similar to HIV-negative patients. However, interpretation of these findings is limited by the fact that we were unable to identify a causative pathogen in approximately half of our patients and that the causative role of CMV ideally is confirmed by tissue examination, which was not routinely done. Although our data do not show differences in disease severity, mechanical ventilation in the first 24 hours after ICU admission was applied less frequently in HIV-positive patients with pneumonia.
We sought to examine the effect of HIV infection on the host response in a matched subgroup of patients with pneumosepsis. Previous reports on the host response to sepsis in adult patients with HIV are limited to two investigations from Brazil in which plasma cytokine levels were studied [27, 28]. Few differences according to HIV status were observed, but one of these studies reported higher plasma IL-10 in the presence of unaltered IL-6 among HIV-positive patients with sepsis [28]. Notably, these encompassed only patients with advanced AIDS-defining disease, HIV-negative control groups unmatched for age and site of infection, and very high mortality rates (around 50 %) [27, 28].
We analyzed host response biomarkers in a relatively homogeneous cohort of patients with pneumosepsis matched for age, gender and white race, and found no differences in the plasma levels of proinflammatory and anti-inflammatory cytokines, with the sole exception of IFN-γ. The main producers of IFN-γ are activated natural killer (NK) cells, T-helper-1 cells, and cytotoxic T cells [29]. Our finding of higher plasma IFN-ɣ in patients with sepsis and HIV co-infection, which was sustained up to two days after ICU admission, is remarkable, as patients with HIV generally have reduced numbers of circulating NK cells and T-helper-1 cells [13]. Furthermore, NK cells from untreated HIV patients released less IFN-γ in response to bacterial stimulation than NK cells from HIV-negative controls [30]. The clinical and biological relevance of (modestly) elevated IFN-γ levels in HIV-infected patients with sepsis remains to be established.
Chronic HIV infection is associated with endothelial cell activation and damage [13], responses that are almost invariably also found in patients with sepsis [31]. In Malawian children with severe bacterial infection, a greater increase in plasma angiopoietin-2, an angiogenic peptide that increases endothelial activation and vascular permeability, was observed in patients with HIV co-infection [32]. In our adult ICU patients with pneumosepsis, plasma levels of specific endothelial cell activation markers (angiopoietin-1 and -2, and soluble E-selectin) did not differ according to HIV status. We did observe higher levels of soluble ICAM-1 in HIV-positive patients with pneumosepsis, which can be shed by both endothelial cells and leukocytes. HIV infection can stimulate the release of exosomes containing ADAM metallopeptidase domain 17 (ADAM17), the cleaving protease for ICAM-1, which promotes ICAM-1 shedding [33]. Increased levels of IFN-ɣ, as observed in our study, may also contribute to the release of soluble ICAM-1 [34]. Although previous studies have described a procoagulant state in patients with HIV [35, 36], plasma levels of D-dimer, protein C and antithrombin were similar in HIV-positive and HIV-negative patients with pneumosepsis. These results indicate that HIV infection has no additive effect on activation of the vascular endothelium and coagulation in critically ill patients with pneumonia.
Our study has strengths and limitations. We prospectively analyzed all consecutive patients admitted with sepsis to two ICUs during a 2.5-year period. Nonetheless, the number of HIV-positive patients with sepsis was limited, precluding stratification according to HIV disease progression. HIV testing is not standard for all ICU patients; thus, our control group may have contained cases with unrecognized HIV infection. However, The Netherlands has a low HIV prevalence of around 0.2 %, so this is unlikely to influence our results [37]. This study was conducted in two academic ICUs and therefore generalization of results should be done with caution. Sepsis was defined using the 2001 consensus definition [18]; the vast majority of included patients had a SOFA score ≥2 at ICU admission, which approximates the recently updated consensus definitions for sepsis [38]. Finally, known HIV infection may lead to selection bias in admittance to ICU and/or the extent of aggressive therapy.
Conclusions
Pneumonia is the main cause of sepsis in HIV-positive ICU patients, and is more frequent compared to patients without HIV infection. Otherwise, our results indicate that in a high-resource setting with excellent access to care and HIV treatment, HIV infection has little, if any, influence on the clinical and pathophysiological course of sepsis requiring ICU admission. These findings support the notion that the presence of HIV co-infection should not play a major role in the decision whether or not to admit critically ill patients with sepsis to the ICU.
Acknowledgements
The authors acknowledge all members of the MARS consortium for the participation in data collection and especially acknowledge: Friso M. de Beer, MD, Lieuwe D. J. Bos, PhD (Department of Intensive Care, Academic Medical Center, University of Amsterdam), Jos F. Frencken, MD (Department of Intensive Care Medicine and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands), Gerie J. Glas, MD, Roosmarijn T. M. van Hooijdonk, MD (Department of Intensive Care, Academic Medical Center, University of Amsterdam), David S.Y. Ong, MD, PharmD (Department of Intensive Care Medicine, Julius Center for Health Sciences and Primary Care and Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands), Laura R. A. Schouten, MD (Department of Intensive Care, Academic Medical Center, University of Amsterdam), Brendon P. Scicluna, PhD (Center for Experimental and Molecular Medicine, Academic Medical Center, University of Amsterdam), Marleen Straat, MD, Esther Witteveen, MD and Luuk Wieske, MD, PhD (Department of Intensive Care, Academic Medical Center, University of Amsterdam).
Funding
This work was supported by the framework of CTMM, the Center for Translational Molecular Medicine (www.ctmm.nl), project MARS (grant 04I-201). The sponsor CTMM was not involved in the design and conduction of the study; nor was the sponsor involved in collection, management, analysis and interpretation of the data or preparation, review or approval of the manuscript. The decision to submit the manuscript was not dependent on the sponsor.
Availability of data and materials
The datasets supporting the results of this article are available on request and addressed to m.a.wiewel@amc.uva.nl.
Authors’ contributions
MAW and MAH designed the study, acquired patient data, performed laboratory experiments, analyzed the data and drafted the manuscript; TvdP designed the study and drafted the manuscript; AJH and RL performed laboratory experiments; LAvV, PMCKK, JH, OLC, MJS and MJB were involved in acquisition of patient data and substantially contributed to the design of the study. All authors reviewed and revised the manuscript critically for important intellectual content. All authors gave final approval of this version to be submitted.
Competing interests
The authors declare that they have no competing interests.
Consent for publication
All authors approve the publication of this manuscript.
Ethical approval and consent to participate
The Medical Ethical Committees of both study centers (AMC Medical Ethics Committee and Medical Ethics Committee UMCU) approved the study protocol, which included an opt-out consent method.
Abbreviations
- cART
combination antiretroviral therapy
- CMV
cytomegalovirus
- HIV
human immunodeficiency virus
- ICAM
intercellular adhesion molecule
- ICU
Intensive Care Unit
- IFN
interferon
- IL
interleukin
- SOFA
Sequential Organ Failure Assessment
- TNF
tumor necrosis factor
Additional files
Characteristics of HIV-positive patients with pneumosepsis with and without readmission. (DOCX 17 kb)
Plasma biomarkers in the matched pneumosepsis cohort during the first admission (readmissions excluded). (DOCX 17 kb)
Contributor Information
Maryse A. Wiewel, Email: m.a.wiewel@amc.uva.nl
Michaëla A. Huson, Email: m.a.huson@amc.uva.nl
Lonneke A. van Vught, Email: l.a.vanvught@amc.uva.nl
Arie J. Hoogendijk, Email: a.j.hoogendijk@amc.uva.nl
Peter M. C. Klein Klouwenberg, Email: P.M.C.KleinKlouwenberg@umcutrecht.nl
Janneke Horn, Email: j.horn@amc.uva.nl.
René Lutter, Email: r.lutter@amc.uva.nl.
Olaf L. Cremer, Email: O.L.Cremer@umcutrecht.nl
Marcus J. Schultz, Email: marcus.j.schultz@gmail.com
Marc J. Bonten, Email: M.J.M.Bonten@umcutrecht.nl
Tom van der Poll, Email: t.vanderpoll@amc.uva.nl.
on behalf of the MARS Consortium:
Friso M. de Beer, Lieuwe D. J. Bos, Jos F. Frencken, Gerie J. Glas, Roosmarijn T. M. van Hooijdonk, David S. Y. Ong, Laura R. A. Schouten, Brendon P. Scicluna, Marleen Straat, Esther Witteveen, and Luuk Wieske
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets supporting the results of this article are available on request and addressed to m.a.wiewel@amc.uva.nl.