Cytokine profiles of umbilical cord blood mononuclear cells upon in vitro stimulation with lipopolysaccharides of different vaginal gram-negative bacteria

Authors: Edith Reuschel aff001;  Martina Toelge aff002;  Kathrin Entleutner aff001;  Ludwig Deml aff002;  Birgit Seelbach-Goebel aff001
Authors place of work: Department of Obstetrics and Gynecology, University of Regensburg, Hospital of the Barmherzige Brueder, Clinic St Hedwig, Regensburg, Germany aff001;  Institute of Medical Microbiology, University Hospital Regensburg, Regensburg, Germany aff002
Published in the journal: PLoS ONE 14(9)
Category: Research Article
doi: 10.1371/journal.pone.0222465


Inflammatory immune responses induced by lipopolysaccharides (LPS) of gram-negative bacteria play an important role in the pathogenesis of preterm labor and delivery, and in neonatal disorders. To better characterize LPS-induced inflammatory response, we determined the cytokine profile of umbilical cord blood mononuclear cells (UBMC) stimulated with LPS of seven vaginal gram-negative bacteria commonly found in pregnant women with preterm labor and preterm rupture of membrane. UBMC from ten newborns of healthy volunteer mothers were stimulated with purified LPS of Escherichia coli, Enterobacter aerogenes, Klebsiella pneumoniae, Proteus mirabilis, Acinetobacter calcoaceticus, Citrobacter freundii, and Pseudomonas aeruginosa. UBMC supernatants were tested for the presence of secreted pro-inflammatory cytokines (IL-6, IL-1β, TNF), anti-inflammatory cytokine (IL-10), TH1-type cytokines (IL-12, IFN-γ), and chemokines (IL-8, MIP-1α, MIP-1β, MCP-1) by Luminex technology. The ten cytokines were differentially induced by the LPS variants. LPS of E. coli and E. aerogenes showed the strongest stimulatory activity and P. aeruginosa the lowest. Interestingly, the ability of UBMC to respond to LPS varied greatly among donors, suggesting a strong individual heterogeneity in LPS-triggered inflammatory response.


Biology and life sciences – Physiology – Developmental biology – Molecular development – Neonates – Embryology – Umbilical cord – Cell biology – Cell motility – Chemotaxis – Chemokines – Microbiology – Bacteriology – Gram negative bacteria – Medical microbiology – Microbial pathogens – Bacterial pathogens – Pseudomonas aeruginosa – Organisms – Bacteria – Pseudomonas – Anatomy – Body fluids – Blood – Medicine and health sciences – Immune physiology – Immunology – Immune system – Innate immune system – Cytokines – Immune response – Inflammation – Pathology and laboratory medicine – Pathogens – Diagnostic medicine – Signs and symptoms


Preterm birth is the most common cause of neonatal death [1]. It is associated with increased neonatal short- and long-term morbidity including severe damages to the brain, bowel, lungs, eyes and developmental defects [25]. Preterm labor (PTL) is defined as labor arising from premature uterine contractility and occurs prior to 37 weeks of gestation in human. In the United States, approximately 10% of all births are diagnosed as preterm [6] and 15 million premature babies are estimated to be born annually worldwide as a result of PTL [7].

As many as 40% of spontaneous preterm births may be attributed to antenatal infection [8] and nearly half of the three million neonatal deaths that occur annually are due to bacterial infections [9]. Ascending genital tract infections of the vagina represent a major cause of PTL, spontaneous preterm birth and preterm rupture of membrane (PROM). Intra-amniotic infection has been causally linked to spontaneous PTL [10]. Indeed, preterm deliveries ensue frequently from an increase in bacterial colonization, which originates as bacterial vaginosis and spreads over gestational tissues including choriodecidua, fetal membranes, amniotic cavity, and eventually the fetus. Bacterial vaginosis up to the 26th week of gestation increases a woman´s risk of preterm delivery by 50% [11], and intrauterine infection is often associated with chorioamnionitis [12,13]. Neonates born to mothers with clinical chorioamnionitis are at risk for sepsis [1416], meconium aspiration syndrome [17], neonatal encephalopathy [18], long-term neurodevelopmental disabilities including cognitive impairment [19,20] and cerebral palsy [21].

PTL exhibit a common feature whereby an increase in inflammatory mediators, such as TNF, IL-1, IL-6 and IL-8, is observed in the amniotic fluid before the onset of uterine contraction. Thus, it is currently assumed that PTL is triggered by premature emergence of these pro-inflammatory mediators in gestational tissues [22]. These pro-inflammatory cytokines might also be the link between prenatal intrauterine infection and intraventricular hemorrhage, resulting in neonatal white matter damage and subsequent cerebral palsy in preterm delivered newborns [23,24]. Maternal systemic inflammation during critical windows of pregnancy may even predispose the neonate to autism spectrum disorders [25] and schizophrenia [26].

Gram-negative bacteria are known to cause severe neonatal infections and associated complications, such as meningitis, cerebral abscesses, septicaemias and sudden unexpected death in neonates and infants [2732]. Gram-negative bacteria express a glycolipid component called endotoxin or lipopolysaccharide (LPS) which participates in the physiological functions of the outer bacterial membrane and is the principal inflammatory component of the gram-negative bacterial envelope [33,34]. LPS signals through Toll-like receptor 4 (TLR4), a member of the TLR family belonging to the pattern recognition receptor family. LPS stimulation via TLR4 results in inflammatory cytokine production, which is responsible for activating the innate immune system [35]. Various cytokines are produced in PTL caused by bacterial infections, via the LPS/TLR4 pathway, causing maternal but also fetal pathologies, such as brain damage, pulmonary or intestinal complications [3638]. LPS-mediated inflammatory response is clearly correlated to prematurity or fetal loss [3942]. A role of the CX3CL1-CX3CR1 chemokine signaling pathway through intrauterine recruitment of macrophages and the enhancement of macrophage-derived inflammatory mediators was recently demonstrated in LPS-induced PTL in mice [43].

LPS are large molecules consisting of a lipid (Lipid A) covalently bound to a polysaccharide [33,34]. Because of the limited variability in their structure, it was initially assumed that all LPS molecules have comparable biological activities. However, it has now been shown that LPS from different bacterial species are structurally and functionally distinct. In vitro experiments have demonstrated great variance in the capacity of different LPS species to induce the synthesis of cytokines [44]. The shape of the Lipid A determines the bioactivity of the LPS [45]. Lipid A that adopts a conical shape conformation (e.g. E. coli) is more active than one that adopts a cylindrical conformation [46]. Gram-negative bacteria have developed numerous mechanisms for the modification of lipid A. These mechanisms include the expression of enzymes adding or removing acyl chains phosphate groups, or altering the acylation state of their LPS in response to environmental changes, or catalyzing the addition of chemical groups into the phosphates [47]. These modifications affect the recognition of LPS by TLR4 and thus impact the downstream inflammatory and immune responses [48]. Differences in TLR4 function and regulation in adult and neonatal monocytes have also been described [4951]. These may account for the attenuated cytokine responses in neonates and the immaturity of infection control noted in preterm and term newborns in association with impaired TLR signaling [52].

We previously examined the distribution of gram-negative bacteria in vaginal and cervical swabs of 239 pregnant women with PROM or PTL at our clinic and identified seven species at the following frequency: E. coli (90%), Klebsiella spp. (12%), Proteus spp. (9%), Pseudomonas spp. (5%), Morganella morganii (2%), Enterobacter spp. (2%), Citrobacter spp. (2%) and Acinetobacter (2%) [53].

We hypothesized that LPS of different gram-negative bacteria present in the vagina of pregnant women induce the release of different cytokine and chemokine profiles, possibly resulting in distinct immunomodulatory activities. We verified this hypothesis by using an in vitro system of freshly isolated umbilical cord blood mononuclear cells (UBMC) stimulated with purified LPS of clinically relevant gram-negative vaginal bacteria. UBMC isolated from ten uncomplicated at-term deliveries were stimulated with purified LPS and the release of a broad panel of immunomodulatory cytokines and chemokines was measured using the Luminex technology.

Materials and methods

Umbilical cord blood source

Informed consent was obtained from ten voluntary healthy mothers. Participants were non-smokers, were not under medical treatment, showed no signs of infection during pregnancy and delivered at term. Umbilical cord blood was collected immediately at birth in citrate bags, following ligation of the umbilical cord, and processed within 12 hours. The protocol of the study was conducted in accordance with the World Medical Association Declaration of Helsinki and approved by the Ethical Commission of the University of Regensburg, Center for Clinical Studies (Approval number 06/098).

Isolation of umbilical cord blood mononuclear cells (UBMC)

The freshly citrated umbilical cord blood was diluted 1:3 with PBS, and 25 to 30 ml diluted blood was carefully laid over 15 ml Pancoll (Lymphocyte sep. medium/ Pancoll human, density 1.077 g/ml, PAN, Biotech, Aidenbach, Germany). UBMC were separated by density gradient centrifugation (800 x g, 30 min) at room temperature (RT), harvested as a single interface layer, and washed three times with 45 ml PBS. Contaminating erythroblasts were eliminated by lysis in 1 ml erythrocyte lysis buffer (BD Pharm LyseTM LYSING BUFFER, Cat. No. 555899) for 10 min at RT, followed by two additional washes in 45 ml PBS. Cell pellets of each donor were resuspended in T-cell medium (RPMI 1640 medium, Gibco, Paisley, Scotland) supplemented with 10% heat-inactivated human AB serum, and enumerated using a Neubauer counting chamber. Total cell number was adjusted to 2 x 105 cells per 90 μl in T-cell medium.

Purified LPS

Purified LPS of selected gram-negative bacteria species were kindly provided by the reference center Research Center Borstel, Leibniz Lung Center (Germany). LPS of the following gram-negative bacteria species were extracted from isolates of various origins as described: E. coli GH58 [54], E. aerogenes 1033 [55], P. mirabilis rough mutant R45 [56], K. pneumoniae rough mutant R20/01 [57], A. calcoaceticus NCTC 10305 [58], C. freundii (S-Form LPS purified by gel permeation chromatography) [59], and P. aeruginosa PAO1 [60].

Stimulation of UBMC with LPS

Freshly isolated UBMC (2 x 105) were seeded in triplicate (90 μl per well) into polypropylene plastic 96-well plates (Nunc, Roskilde, Denmark). Unless otherwise indicated, cells were stimulated with 37.5 ng/ml purified LPS in 100 μl final volume for 36 hours at 37°C in a humidified atmosphere containing 5% CO2. UBMC stimulated with PBS served as a negative control. The synthetic bacterial lipopeptide and TLR1/2 agonist PAM3CSK4 [61] (L2000, EMC Microcollections, Tuebingen) was tested in parallel at the concentration of 37.5 ng/ml. Cell-free supernatants of stimulated cells were harvested by low speed centrifugation (300 x g, 10 min) and stored at -80°C.

Determination of cytokine and chemokine concentrations in UBMC supernatants

The levels of cytokines and chemokines in the UBMC supernatants were determined applying the Luminex technology (MicroBIOMix GmbH, Regensburg). A pilot experiment on one subject was performed using the Human Cytokine 30-Plex panel (LHC6003, Invitrogen/ThermoFisher), which includes the following cytokines, chemokines and growth factors: IL-1β, IL-1-Receptor Antagonist (IL-1RA), IL-2, IL-2 receptor (IL-2R), IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 (protein 40/protein 70), IL-13, IL-15, IL-17, TNF, interferons IFN-α and IFN-γ, granulocyte-macrophage colony stimulating factor (GM-CSF), macrophage inflammatory proteins MIP-1α and MIP-1β, interferon-γ-induced protein 10 (IP-10), monokine induced by interferon-γ (MIG), eotaxin, regulated and normal T-cell expressed and secreted (RANTES), monocyte chemoattractant protein 1 (MCP-1), vascular endothelial growth factor (VEGF), granulocyte colony stimulating factor (G-CSF), epidermal growth factor (EGF), fibroblast growth factor (FGF) and human growth factor (HGF). Further Luminex assays were conducted using the following human singleplex beads kits (Invitrogen/ThermoFisher): IL-1β (LHC0011), IL-10 (LHC0101), IL-6 (LHC0061), IL-8 (LHC0081), IL-12 [p40/p70] (LHC0121), TNF (LHC3011), IFN-γ (LHC4031), MIP-1α (LHC1021), MIP-1β (LHC1051), and MCP-1 (LHC1011). Experiments were performed using the Human Extracellular Protein Buffer Reagent Kit (LHB0001, Invitrogen/ThermoFisher) according to the manufacturers' protocol. The assays were performed in 96-well filter bottom plates. The beads were protected from light throughout the procedure. The lyophilized standard was reconstituted in 2 ml assay diluents and 1:3 serial dilutions were undertaken to generate a seven standard concentration set, while diluent alone served as blank. The filtered plates were pre-washed with 200 μl of wash solution/well for 30 seconds. Wash solutions were aspirated using a vacuum manifold and the bottom of the plate was blotted on paper towels to remove residual liquid. The concentrated bead mix was diluted 1:20 in wash solution. The bead solution was vortexed and sonicated immediately prior to adding 50 μl/well. The plate was washed twice with 200 μl wash solution/well as above. Incubation buffer (50 μl) and each standard (100 μl) were added in duplicate. Assay diluent (50 μl) was added to each well followed by the addition of the sample (50 μl). The plate was covered and incubated for 2 h at RT on an orbital plate shaker (600 rpm). Afterwards, the liquid was removed using a vacuum manifold, and the plate was washed twice. A biotinylated detection antibody (100 μl) was added and plate was covered and incubated on the shaker for 1 h at RT. The plate was washed twice prior to addition of Streptavidin-RPE (100 μl), then covered and incubated for 30 min at RT on the shaker. Finally, the plate was washed three times. Wash solution (110 μl) was added to each well, the plate was covered, placed on the orbital shaker and incubated for 2–3 min at RT prior to analysis. Mean fluorescence intensity (MFI) was acquired using the Luminex xMAP 100 system (Luminex Corp.). Software was set to acquire data using 70 μl sample and count 100 events per single bead set.

Statistical analyses

Cyto- and chemokine-concentrations were calculated using a 4- or 5-parameter logistic fit curve generated from the 7 standards using the Liquichip Analyzer software (Qiagen, Germany) and expressed in ng/ml in accordance with International Standards. Statistical differences between measured values in stimulated and unstimulated conditions were analyzed using a Mann-Whitney U-test. P values less than 0.05 were considered statistically significant. Statistical tests were performed using SPSS 15 (for Windows).


Purified LPS from seven gram-negative vaginally occurring bacteria commonly found in pregnant women with PTL and PROM, namely E. coli GH58, E. aerogenes 1033, P. mirabilis rough mutant R4, K. pneumoniae rough mutant R20/01, A. calcoaceticus NCTC 10305, C. freundii (S-Form), and P. aeruginosa PAO1 [53], were used to stimulate UBMC freshly isolated at birth from ten healthy at-term neonates. Secreted cytokines were quantified in the cell culture supernatant of stimulated UBMC using the Luminex technology. The characteristics of the mothers and respective newborns are shown in Table 1. Median (range) time from blood collection to processing was 7.0 (2.5–12.0) hours.

Tab. 1.

Characteristics of the 10 mothers and respective neonates, as well as storage time of umbilical cord blood from collection at delivery until isolation of UBMCa.

<h2>Characteristics of the 10 mothers and respective neonates, as well as storage time of umbilical cord blood from collection at delivery until isolation of UBMC<em class="ref"><sup>a</sup></em>.</h2>

Pilot experiments were performed on Subjects number 1 to 3 to identify an optimal LPS concentration, duration of stimulation and relevant cytokines (Figs 15; Table 2). UBMC of three donors were stimulated for 36 hours with increasing amounts (from 0.006 to 3027 ng/ml) of purified LPS (Figs 14). A subanalysis was performed on one donor to compare a 4-hour to a 36-hour LPS stimulation on selected cytokines (Fig 5). Based on these experiments, as well as on reports from the literature [6265], we selected a LPS concentration of 37.5 ng/ml and a stimulation duration of 36 hours as optimal to detect significant levels of ten selected cytokines and chemokines (IL-1β, IL-10, IL-6, IL-8, IL-12 [p40/p70], TNF, IFN-γ, MIP-1α, MIP-1β, MCP-1). Although the concentration of 37.5 ng/ml LPS was not sufficient to induce a strong cytokine response in some cases (e.g. P. aeruginosa; Figs 14), this working concentration was chosen to remain in a range of LPS close to that normally detected in the plasma of patients with sepsis [66]. Additional secreted cytokines and growth factors measured in the supernatant of one donor using a 30-plex cytokine panel are shown in Table 2. In this donor, low to high levels of secreted factors were detected (low: IL-2, IL-4, IL-5, IL-13, IP-10, eotaxin, HGF; intermediate: IL-15, MIG, FGF-basic; high: IL-7, IL-1RA, IL-2R, RANTES, G-CSF, GM-CSF, VEGF), while IL-17, EGF and IFN-α were undetectable (Table 2).

<h2>Dose response of LPS on the release of pro-inflammatory cytokines by UBMC.</h2>
Fig. 1.

Dose response of LPS on the release of pro-inflammatory cytokines by UBMC.

UBMC isolated from three of the ten deliveries (Subjects 1–3; Table 1) were stimulated for 36 hours with increasing amounts (0–3027 ng/ml) of purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). The levels of pro-inflammatory cytokines (IL-6, IL-1β, TNF) released in the supernatants of UBMC were measured by Luminex, as described in the Methods section. UBMC of Subject 1 released levels of IL-6 above the detection range of the Luminex assay (saturated signal), as indicated by the green dotted line and the (*) sign.

<h2>Dose response of LPS on the release of anti-inflammatory and TH1-type cytokines by UBMC.</h2>
Fig. 2.

Dose response of LPS on the release of anti-inflammatory and TH1-type cytokines by UBMC.

UBMC isolated from three of the ten deliveries (Subjects 1–3; Table 1) were stimulated for 36 hours with increasing amounts (0–3027 ng/ml) of purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). The levels of anti-inflammatory cytokine (IL-10) and TH1-type cytokines (IL-12, IFN-γ) released in the supernatants of UBMC were measured by Luminex, as described in the Methods section.

<h2>Dose response of LPS on the release of chemokines by UBMC.</h2>
Fig. 3.

Dose response of LPS on the release of chemokines by UBMC.

UBMC isolated from three of the ten deliveries (Subjects 1–3; Table 1) were stimulated for 36 hours with increasing amounts (0–3027 ng/ml) of purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). The levels of chemokines (IL-8, MCP-1) released in the supernatants of UBMC were measured by Luminex, as described in the Methods section.

<h2>Dose response of LPS on the release of chemokines by UBMC.</h2>
Fig. 4.

Dose response of LPS on the release of chemokines by UBMC.

UBMC isolated from three of the ten deliveries (Subjects 1–3; Table 1) were stimulated for 36 hours with increasing amounts (0–3027 ng/ml) of purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). The levels of chemokines (MIP-1α, MIP-1β) released in the supernatants of UBMC were measured by Luminex, as described in the Methods section. Based on the assays presented in Figs 1–4, the concentration of 37.5 ng/ml LPS was used for further experiments.

<h2>Dose response and time course of LPS on the release of cytokines and chemokines by UBMC.</h2>
Fig. 5.

Dose response and time course of LPS on the release of cytokines and chemokines by UBMC.

UBMC isolated from Subject 2 (Table 1) were stimulated for either 4 or 36 hours with increasing amounts (0–3027 ng/ml) of purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). The levels of IL-12, IL-6 and TNF released in the UBMC supernatant were measured by Luminex, as described in the Methods section. Based on these preliminary assays (and reports from the literature; see text), a stimulation duration of 36 h was used for further experiments.

Tab. 2.

Luminex assay using a human cytokine 30-plex panel on UBMC's supernantant of Subject 1, following stimulation for 36 h with 37.5 ng/ml purified LPS obtained from the indicated baterial species (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa).

<h2>Luminex assay using a human cytokine 30-plex panel on UBMC's supernantant of Subject 1, following stimulation for 36 h with 37.5 ng/ml purified LPS obtained from the indicated baterial species (<i>E</i>. <i>coli</i>, <i>E</i>. <i>aerogenes</i>, <i>K</i>. <i>pneumoniae</i>, <i>P</i>. <i>mirabilis</i>, <i>A</i>. <i>calcoaceticus</i>, <i>C</i>. <i>freundii</i>, <i>P</i>. <i>aeruginosa</i>).</h2>

Abbreviation: SD, standard deviation.

Seven additional UBMC preparations were stimulated with 37.5 ng/ml LPS for 36 hours. The same concentration of the synthetic TLR1/TLR2 agonist PAM3 [61] was tested in parallel. Levels of secreted pro-inflammatory cytokines (IL-6, IL-1β, TNF), anti-inflammatory cytokine (IL-10), TH1-cytokines (IL-12, IFN-γ), and chemokines (IL-8, MIP-1α, MIP-1β, MCP-1) were measured by Luminex. Results obtained from the ten donors in comparison to the unstimulated control are shown in Fig 6.

<h2>Levels of cytokines secreted by LPS-stimulated UBMC.</h2>
Fig. 6.

Levels of cytokines secreted by LPS-stimulated UBMC.

Levels of pro-inflammatory (IL-6, IL-1ß, TNF) and anti-inflammatory (IL-10) cytokines (A), of the TH1-polarizing cytokines IL-12 (p40/p70) and IFN-γ (B), and of the chemokines IL-8, MIP-1α, MIP-1β and MCP-1 (C) released by LPS-stimulated UBMC. UBMC isolated from ten uncomplicated deliveries of at-term newborns were stimulated for 36 h with 37.5 ng/ml purified LPS derived from the indicated seven gram-negative bacteria (E. coli, E. aerogenes, K. pneumoniae, P. mirabilis, A. calcoaceticus, C. freundii, P. aeruginosa). Unstimulated UBMC served as reference (Control). The TLR1/2 agonist PAM3 served as additional control in seven out of ten donors. Cytokines levels in the respective UBMC supernatants were measured by Luminex. Differences between unstimulated and stimulated conditions were evaluated using the non-parametric Mann-Whitney U-test. Respective P values are indicated above each box plot. Medians (horizontal white line), arithmetic means (horizontal black line) and interquartile ranges are shown. IL-6 levels in Subject 1 were above the detection range after stimulation with six out of seven LPS variants (see also Figs 14 and Table 2), and thus the respective concentrations were excluded from the graphic representation and statistical analysis.

Six out of the seven purified LPS (E. coli, E. aerogenes, P. mirabilis, K. pneumoniae, A. calcoaceticus, C. freundii) induced significant levels of the ten cytokines and chemokines investigated (Fig 6A–6C). With the exception of IL-6, LPS from P. aeruginosa did not induce significant production of pro- and anti-inflammatory cytokines (Fig 6A). It induced however low but significant levels of chemokines by UBMC (Fig 6C). In comparison, the TLR1/2 agonist PAM3 induced no or weak cytokine production (Fig 6A and 6B), and significant chemokine production (Fig 6C).

The donor-to-donor variability in the levels of detected cytokines was high for all tested cytokines and chemokines (Figs 14 and 6). For instance, the level of TNF in the UBMC supernatant upon stimulation with LPS from E. coli ranged from 38 to 2763 pg/ml (median TNF concentration of 309 pg/ml) among the ten donors. Moreover, LPS from different bacterial species induced distinct cytokines profiles in a given UBMC preparation (Figs 14 and 6). Among the ten donors, LPS from E. coli and E. aerogenes induced the highest median level of cytokines and chemokines, followed by P. mirabilis and K. pneumoniae. LPS from A. calcoaceticus and C. freundii induced further lower median cytokine and chemokines levels, and–as mentioned above–LPS from P. aeruginosa was the least active (Fig 6A–6C).

After 36 hours of LPS stimulation, the most prominent detected cytokines were the pro-inflammatory cytokine IL-6 and the chemokines IL-8, MIP-1α, MIP-1β and MCP-1 (median levels >2,900 pg/ml; Fig 6A–6C). TNF, IL-1β, IL-10 and IL-12 were detected at intermediate levels (median between 33 and 929 pg/ml; Fig 6A and 6B), and IFN-γ was the lowest (median level ≤20 pg/ml in response to all LPS variants; Fig 6B).


We describe here the profile of cytokines and chemokines released by UBMC following their in vitro stimulation by LPS of seven common vaginal gram-negative bacteria species. Four groups of secreted factors were investigated: pro-inflammatory cytokines (IL-6, IL-1β, TNF), an anti-inflammatory cytokine (IL-10), TH1-type cytokines (IL-12, IFN-γ) and chemokines (IL-8, MIP-1α, MIP-1β, MCP-1). Herein, we could confirm our hypothesis that LPS of different gram-negative bacterial species induce distinct inflammatory responses and thus might exert different immunomodulatory functions. We showed that in vitro stimulation of freshly isolated UBMC with purified LPS of these bacteria induced different levels of secreted pro- and anti-inflammatory cytokines and chemokines. Interestingly, the range of cytokine and chemokine concentrations detected in the supernatants of stimulated UBMC varied drastically between donors, indicating major differences in individual responsiveness to a given LPS variant.

All ten cytokines and chemokines were induced in UBMC after 36 hours stimulation with the different LPS, albeit at different levels, as summarized in Fig 7.

<h2>Summary of the cytokine profiles in UBMC stimulated with LPS of seven gram-negative bacteria.</h2>
Fig. 7.

Summary of the cytokine profiles in UBMC stimulated with LPS of seven gram-negative bacteria.

Median cytokine levels in LPS-stimulated UBMC isolated from ten uncomplicated deliveries. Median cytokine levels are directly derived from the data presented in Fig 6. Due to log scale representation, values of 0 pg/ml were replaced by 0.1; thus values depicted at 0.1 pg/ml along the x axis are actually equal to zero. IL-8, IL-6, MIP-1α, MIP-1β and MCP-1 showed the highest median level of induction, followed by TNF, IL-1β, IL-10 and IL-12. IFN-γ showed the lowest median level of secretion.

The pro-inflammatory cytokine IL-6 and the chemokines IL-8, MIP-1α, MIP-1β and MCP-1 showed the highest induction, with median levels ranging from 77 to 196,000 pg/ml upon LPS stimulation. Elevated IL-6 and IL-8 levels after LPS stimulation of umbilical cord blood was also reported by others [49,51,67]. Our results thus support the observation that intrauterine infection results in the secretion of pro-inflammatory cytokines and chemokines such as Il-1ß, Il-6, IL-8, TNF and MCP-1, in association with PTL and fetal brain injury [23,36,39,6870].

The anti-inflammatory and TH2-polarizing cytokine IL-10 was induced at low levels (median 0 to 120 pg/ml) by all seven LPS tested. IL-10 is an important regulator and suppressor of the pro-inflammatory cascade [36]. IL-10 is normally produced at the maternal-fetal interface, and exerts together with progesterone a strong immunomodulatory protection of the fetal allograft [36].

IL-12 is an essential cytokine for the generation of the TH1-type immune responses. It is produced by monocytes and dendritic cells (DC) upon stimulation with LPS [71]. In our study median IL-12 (p40/p70) levels ranged from 126 to 605 pg/ml in the supernatants of LPS-stimulated UBMC, with maximum levels ranging from 1,450 and 4,593 pg/ml between LPS variants. Others showed that IL-12 is weakly expressed and secreted in LPS-stimulated whole cord blood [49,72].

As opposed to IL-12, levels of the TH1 cytokine IFN-γ were consistently low in all donors and upon stimulation with all seven LPS. This is in line with published report in LPS-stimulated PBMC [73]. However, we cannot exclude that a different duration of LPS stimulation might allow a better detection of secreted IFN-γ levels. For instance, the level of secreted TNF in Subject 2 was higher after 4 hours of LPS stimulation with all seven LPS variants than after 36 hours.

Other studies compared the response to LPS of UBMC to that of adult peripheral blood mononuclear cells. Some studies showed a reduced cytokine production (e.g. IL-12) in LPS-stimulated whole cord blood compared to adult whole blood [49,72], supporting the proposition that TLR4-mediated response is impaired in neonates and infants [50,52,72]. Other studies however described an elevated cytokine responses, in particular of IL-6, TNF, IL-8 and IL-10 [49,51,67], and even a newborn-specific cytokine production [74] after LPS stimulation of umbilical cord blood. These differences in reported LPS responsiveness might be a consequence of differential TLR4 regulation, due to differences in TLR4 expression in neonates and adults [49,51,75] and/or due to TLR4 gene polymorphism [76].

Alternatively, these functional differences in LPS responsiveness might also be due to the use of LPS of different origin and species in these reported studies. Indeed, in our study the comparison of the stimulatory activity of purified LPS from seven common gram-negative bacteria species revealed functional differences. LPS of E. coli and E. aerogenes provoked the highest cytokine and chemokine release, while LPS of P. aeruginosa was the least active. The low stimulatory activity of LPS of P. aeruginosa might be explained by its reduced acylation state, which is an important component of TLR4 recognition, compared to other LPS [47]. The observed differences in LPS activity therefore confirm our hypothesis that different LPS molecules potentially mediate different inflammatory responses, in line with reports from the literature [44,4648]. Our data are also in agreement with the virulence and neonatal complications associated with E. coli, including neonatal sepsis [7779] and with E. aerogenes infections [80,81].

In addition, we observed striking differences in the responsiveness of the ten UBMC preparations, resulting in skewed levels of cytokine release. Higher cytokine release in some donors did not correlate with longer cord blood storage before UBMC isolation (Fig 5 and Table 1). Therefore higher cytokine release cannot be accounted for artefactual cytokine release by contaminating granulocytes, which are known to accumulate in the mononuclear cell layer during density gradient centrifugation in case of delayed blood processing [82,83]. The reason for such variability in cytokine levels is unknown and remains to be investigated. It might be the consequence of differences in TLR4 function between donors, due to differential gene expression and/or polymorphism [75,76]. Nevertheless, the observation that UBMC of neonates born after uncomplicated gestation and delivery produce such variable levels of cytokines upon LPS stimulation raises the possibility that pregnant women might experience different levels of inflammatory response following a bacterial infection, potentially differentially affecting pregnancy outcome. It would be interesting to compare these results to those generated from UBMC of premature neonates with a declared bacterial infection.

Prevention of infection remains the most promising approach to reduce PTL and associated mortality and morbidity in this highly vulnerable neonatal population. Diagnostic and treatment of prenatal and neonatal infections is a major challenge. The present study suggests that measuring cytokine levels might guide the diagnosis of bacterial infections. Interestingly, others showed that it is possible to measure cytokine levels in amniotic fluid collected noninvasively from vaginal secretions of women with preterm premature rupture of membranes. Increased levels of amniotic fluid IL-6 and TNF were good predictors of fetal inflammatory response syndrome [84]. By using the umbilical cord as a noninvasive source of neonatal blood, as in our study, one may be able to establish the cytokine profile of neonates and evaluate their risk of infection-related complications after birth.

In terms of treatment of prenatal and neonatal infections, antibiotics acting against gram-negative bacteria exist. However, antenatal antibiotic treatment alone has limited success at preventing PTL or improving neonatal outcome [85]. A combination of anti-inflammatory therapy and effective antibiotics has been proposed to combat intra-uterine infection and reduce associated inflammatory responses leading to PTL and adverse fetal sequelae. Optimal treatments also increase the survival of premature infants by promoting lung maturation, as illustrated by the combination of betamethasone with tocolytic agents such as nonsteroidal anti-inflammatory drugs (NSAIDs) like indomethacin. The anti-inflammatory effect of the combination therapy of betamethasone with indomethacin might also reduce bacterial clearance. Our group showed furthermore that, similar to betamethasone alone, the combination therapy effectively reduced the expression of the pro-inflammatory cytokines TNF, IL-6 and IL-12 [86]. Other studies even suggested that a postnatal application of indomethacin to preterm neonates delivered before 28 weeks of gestation provided beneficial effects on the fetal brain [87]. This neuroprotective effects of indomethacin might be due to an increase of cerebral vascular resistance and stability of cerebral hemodynamics [88,89]. Additionally to NSAIDs, cytokine suppressive anti-inflammatory drugs (CSAIDs) are novel compounds that specifically target cytokine signaling pathways, exerting anti-inflammatory actions in both human fetal membranes in vitro and animal models of intrauterine infection. These compounds have the potential to be safer and more effective than less selective inhibitors of inflammation [90].

In conclusion, we showed that LPS of different vaginal gram-negative bacteria trigger different cytokine and chemokine responses and that individual UBMC differentially respond to LPS stimulation. Further studies are needed to better understand the relationship between intrauterine infection, inflammatory response and PTL, and to develop clinical approaches to reduce preterm delivery and associated neonatal complications.


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