Spontaneous neutrophil migration patterns during sepsis after major burns

Caroline N Jones, Molly Moore, Laurie Dimisko, Andrew Alexander, Amir Ibrahim, Bryan A Hassell, H Shaw Warren, Ronald G Tompkins, Shawn P Fagan, Daniel Irimia, Caroline N Jones, Molly Moore, Laurie Dimisko, Andrew Alexander, Amir Ibrahim, Bryan A Hassell, H Shaw Warren, Ronald G Tompkins, Shawn P Fagan, Daniel Irimia

Abstract

Finely tuned to respond quickly to infections, neutrophils have amazing abilities to migrate fast and efficiently towards sites of infection and inflammation. Although neutrophils ability to migrate is perturbed in patients after major burns, no correlations have yet been demonstrated between altered migration and higher rate of infections and sepsis in these patients when compared to healthy individuals. To probe if such correlations exist, we designed microfluidic devices to quantify the neutrophil migration phenotype with high precision. Inside these devices, moving neutrophils are confined in channels smaller than the neutrophils and forced to make directional decisions at bifurcations and around posts. We employed these devices to quantify neutrophil migration across 18 independent parameters in 74 blood samples from 13 patients with major burns and 3 healthy subjects. Blinded, retrospective analysis of clinical data and neutrophil migration parameters revealed that neutrophils isolated from blood samples collected during sepsis migrate spontaneously inside the microfluidic channels. The spontaneous neutrophil migration is a unique phenotype, typical for patients with major burns during sepsis and often observed one or two days before the diagnosis of sepsis is confirmed. The spontaneous neutrophil migration phenotype is rare in patients with major burns in the absence of sepsis, and is not encountered in healthy individuals. Our findings warrant further studies of neutrophils and their utility for early diagnosing and monitoring sepsis in patients after major burns.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Measuring neutrophil migration in burn…
Figure 1. Measuring neutrophil migration in burn patients during sepsis.
(A) Overview of the protocol using microfluidic devices to measure neutrophil migration in patients with major burns. (1) Three milliliters blood samples are obtained from patients with major burns. (2) Neutrophils are separated from blood using negative selection beads. (3) Microfluidic devices are primed with chemoattractant solutions and patient neutrophils are introduced into the neutrophil loading channel. (4) Neutrophils are observed using time-lapse imaging during migration through 3×6 µm channels and mazes of channels. (5) Images of moving neutrophils are recorded at single cells resolution and analyzed to quantify 18 neutrophil migratory parameters. (6) A neutrophil spontaneous motility score is calculated for each sample. (7) Correlations are tested between the Neutrophil activation score (NASN) and sepsis in patients with major burns. This cycle is repeated every two days or less often for the duration of burn patient treatment, up to one month. (B) Typical timeline for sample collection from burn patients. During the first phase, samples are collected every two days for one week. A second phase continues with one sample every week for up to one month. A third phase is triggered by the clinicians when there is request for blood cultures, signs of fever, leukocytosis and/or thrombocytosis. During Phase three, samples are collected every two days for a week.
Figure 2. Neutrophil migration parameters in burn…
Figure 2. Neutrophil migration parameters in burn patients.
(A) Heat-map showing the results of 18 neutrophil migratory phenotype measurements in 74 blood samples from 13 burn patients and three healthy volunteers. Specific measurements are explained in detail in Table 2, including averages for each parameter. Each parameter was measured in three conditions: in the absence of chemoattractant, and in the presence of fMLP and LTB4 chemoattractant gradients. Bright green illustrates 2 S.D. below healthy donor averages, light green illustrates 1 S.D. below healthy donor averages, bright red illustrates 2 S.D. above healthy donor averages, and light red illustrates 1 S.D. above healthy donor averages. Below the heat map, a color coded bar represents the status of the blood donor at the time of the draw. Red illustrates sepsis, green illustrates SIRS, and black illustrates no SIRS status. The day post burn is indicated above the bar, the patient identifier is presented below the bar. Healthy donors, burn patients with sepsis, and burn patients without sepsis are grouped by the accolades. (B) Kymograph showing an example of oscillatory migration of a neutrophil from a septic burn-patient, in the absence of chemoattractant. The time interval between successive frames is 2 minutes. Vertical scale bar is 100 µm.
Figure 3. The components and temporal evolution…
Figure 3. The components and temporal evolution of neutrophil spontaneous migration score (NASN) in patients with major burns.
(A) Two dimensional comparisons between neutrophil migration parameters between healthy donors (black stars), burn patients with no complications (green square), SIRS (green triangle), and sepsis (red square). In the absence of chemoattractant, neutrophils from patients with sepsis migrate in larger numbers and display more oscillatory migration than the patients with SIRS or those from healthy donors (which do not migrate). (B) Neutrophils from patients with sepsis migrate longer distances and display more oscillatory migration than the patients with SIRS or those from healthy donors (which do not migrate). (C) Changes in the neutrophil activation score in the 6 patients with no sepsis during the hospital stay. On patient that died is indicated (red cross). (D) Changes in the neutrophil activation score in the 7 patients that experience sepsis during the hospital stay. Higher scores are observed during sepsis (filled red triangle). In patients that respond to antibiotic treatment, NASN decreases when sepsis is resolved (empty red triangles). In some of the patients, NASN increased even several days before sepsis was diagnosed (red star). The NASN remained low in these patients in the absence of complications (empty gray triangle).
Figure 4. Correlations between the changes in…
Figure 4. Correlations between the changes in neutrophil spontaneous migration score (NASN) and the timing of sepsis in burn patients.
(A) Neutrophil activation score averages are significantly different between burn patients with sepsis (N = 21) and patients with SIRS (N = 29, P = 0.038) or patients with no SIRS (N = 21, P = 0.027). (B) The NASN is significantly higher in patients in samples before clinical diagnosis (P = 0.036) and drops to one third following septic diagnosis and post-antibiotic therapy. (C) ROC curves for averaged NASN of two successive blood samples demonstrates the good predictive values of the spontaneous neutrophil migration patterns for sepsis in patients with major burns.

References

    1. D'Avignon LC, Hogan BK, Murray CK, Loo FL, Hospenthal DR, et al. (2010) Contribution of bacterial and viral infections to attributable mortality in patients with severe burns: An autopsy series. Burns 36:773–779.
    1. Williams FN, Herndon DN, Hawkins HK, Lee JO, Cox RA, et al. (2009) The leading causes of death after burn injury in a single pediatric burn center. Crit Care 13:R183.
    1. Angus DC, Linde-Zwirble WT, Lidicker J, Clermont G, Carcillo J, et al. (2001) Epidemiology of severe sepsis in the United States: analysis of incidence, outcome, and associated costs of care. Crit Care Med 29:1303–1310.
    1. Kumar A, Ellis P, Arabi Y, Roberts D, Light B, et al. (2009) Initiation of inappropriate antimicrobial therapy results in a fivefold reduction of survival in human septic shock. Chest 136:1237–1248.
    1. Levy MM, Fink MP, Marshall JC, Abraham E, Angus D, et al. (2003) 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference. Intensive Care Med 29:530–538.
    1. Fournier PE, Drancourt M, Colson P, Rolain JM, La SB, et al. (2013) Modern clinical microbiology: new challenges and solutions. NatRevMicrobiol 11:574–585.
    1. Seng P, Rolain JM, Fournier PE, La SB, Drancourt M, et al. (2010) MALDI-TOF-mass spectrometry applications in clinical microbiology. FutureMicrobiol 5:1733–1754.
    1. Branski LK, Al-Mousawi A, Rivero H, Jeschke MG, Sanford AP, et al. (2009) Emerging infections in burns. SurgInfect(Larchmt) 10:389–397.
    1. Bernard GR, Vincent JL, Laterre PF, Larosa SP, Dhainaut JF, et al. (2001) Efficacy and safety of recombinant human activated protein C for severe sepsis. NEnglJMed 344:699–709.
    1. Jeschke MG, Finnerty CC, Kulp GA, Kraft R, Herndon DN (2013) Can we use C-reactive protein levels to predict severe infection or sepsis in severely burned patients? IntJBurns Trauma 3:137–143.
    1. Fitrolaki DM, Dimitriou H, Kalmanti M, Briassoulis G (2013) CD64-Neutrophil expression and stress metabolic patterns in early sepsis and severe traumatic brain injury in children. BMCPediatr 13:31.
    1. Fjaertoft G, Hakansson LD, Pauksens K, Sisask G, Venge P (2007) Neutrophil CD64 (FcgammaRI) expression is a specific marker of bacterial infection: a study on the kinetics and the impact of major surgery. ScandJInfectDis 39:525–535.
    1. Karzai W, Oberhoffer M, Meier-Hellmann A, Reinhart K (1997) Procalcitonin–a new indicator of the systemic response to severe infections. Infection 25:329–334.
    1. Oberhoffer M, Karzai W, Meier-Hellmann A, Bogel D, Fassbinder J, et al. (1999) Sensitivity and specificity of various markers of inflammation for the prediction of tumor necrosis factor-alpha and interleukin-6 in patients with sepsis. Crit Care Med 27:1814–1818.
    1. Pascual C, Karzai W, Meier-Hellmann A, Oberhoffer M, Horn A, et al. (1998) Total plasma antioxidant capacity is not always decreased in sepsis. Crit Care Med 26:705–709.
    1. Tavares-Murta BM, Zaparoli M, Ferreira RB, Silva-Vergara ML, Oliveira CH, et al. (2002) Failure of neutrophil chemotactic function in septic patients. Crit Care Med 30:1056–1061.
    1. Danikas DD, Karakantza M, Theodorou GL, Sakellaropoulos GC, Gogos CA (2008) Prognostic value of phagocytic activity of neutrophils and monocytes in sepsis. Correlation to CD64 and CD14 antigen expression. ClinExpImmunol 154:87–97.
    1. Parihar A, Parihar MS, Milner S, Bhat S (2008) Oxidative stress and anti-oxidative mobilization in burn injury. Burns 34:6–17.
    1. Kasten KR, Muenzer JT, Caldwell CC (2010) Neutrophils are significant producers of IL-10 during sepsis. BiochemBiophysResCommun 393:28–31.
    1. Bjerknes R, Vindenes H (1989) Neutrophil dysfunction after thermal injury: alteration of phagolysosomal acidification in patients with large burns. Burns 15:77–81.
    1. Boyden S (1962) The chemotactic effect of mixtures of antibody and antigen on polymorphonuclear leucocytes. J Exp Med 115:453–466.
    1. Li Jeon N, Baskaran H, Dertinger SK, Whitesides GM, Van de Water L, et al. (2002) Neutrophil chemotaxis in linear and complex gradients of interleukin-8 formed in a microfabricated device. Nat Biotechnol 20:826–830.
    1. Abhyankar VV, Lokuta MA, Huttenlocher A, Beebe DJ (2006) Characterization of a membrane-based gradient generator for use in cell-signaling studies. Lab Chip 6:389–393.
    1. Irimia D, Liu SY, Tharp WG, Samadani A, Toner M, et al. (2006) Microfluidic system for measuring neutrophil migratory responses to fast switches of chemical gradients. Lab Chip 6:191–198.
    1. Keenan TM, Folch A (2008) Biomolecular gradients in cell culture systems. Lab Chip 8:34–57.
    1. Lin F, Nguyen CM, Wang SJ, Saadi W, Gross SP, et al. (2005) Neutrophil migration in opposing chemoattractant gradients using microfluidic chemotaxis devices. Ann Biomed Eng 33:475–482.
    1. Saadi W, Rhee SW, Lin F, Vahidi B, Chung BG, et al. (2007) Generation of stable concentration gradients in 2D and 3D environments using a microfluidic ladder chamber. Biomed Microdevices 9:627–635.
    1. Irimia D, Balazsi G, Agrawal N, Toner M (2009) Adaptive-control model for neutrophil orientation in the direction of chemical gradients. Biophys J 96:3897–3916.
    1. Sackmann EK, Berthier E, Young EW, Shelef MA, Wernimont SA, et al. (2012) Microfluidic kit-on-a-lid: a versatile platform for neutrophil chemotaxis assays. Blood 120:e45–e53.
    1. Ambravaneswaran V, Wong IY, Aranyosi AJ, Toner M, Irimia D (2010) Directional decisions during neutrophil chemotaxis inside bifurcating channels. Integr Biol (Camb) 2:639–647.
    1. Irimia D, Charras G, Agrawal N, Mitchison T, Toner M (2007) Polar stimulation and constrained cell migration in microfluidic channels. Lab Chip 7:1783–1790.
    1. Butler KL, Ambravaneswaran V, Agrawal N, Bilodeau M, Toner M, et al. (2010) Burn injury reduces neutrophil directional migration speed in microfluidic devices. PLoS One 5:e11921.
    1. Bjerknes R, Vindenes H, Laerum OD (1990) Altered neutrophil functions in patients with large burns. Blood Cells 16:127–141.
    1. de Chalain TM, Bracher M, Linley W, Gerneke D, Hickman R (1994) Cytoskeletal actin: the influence of major burns on neutrophil structure and function. Burns 20:416–421.
    1. Hietbrink F, Koenderman L, Althuizen M, Pillay J, Kamp V, et al. (2013) Kinetics of the innate immune response after trauma: implications for the development of late onset sepsis. Shock 40:21–27.
    1. Kim Y, Goldstein E, Lippert W, Brofeldt T, Donovan R (1989) Polymorphonuclear leucocyte motility in patients with severe burns. Burns 15:93–97.
    1. Solomkin JS, Nelson RD, Chenoweth DE, Solem LD, Simmons RL (1984) Regulation of neutrophil migratory function in burn injury by complement activation products. Ann Surg 200:742–746.
    1. Warden GD, Mason AD Jr, Pruitt BA Jr. (1975) Suppression of leukocyte chemotaxis in vitro by chemotherapeutic agents used in the management of thermal injuries. Ann Surg 181:363–369.
    1. Kurihara T, Jones CN, Yu YM, Fischman AJ, Watada S, et al. (2013) Resolvin D2 restores neutrophil directionality and improves survival after burns. Faseb J 27:2270–2281.
    1. Warden GD, Mason AD Jr., Pruitt BA Jr. (1974) Evaluation of leukocyte chemotaxis in vitro in thermally injured patients. J Clin Invest 54.
    1. Hamza B, Wong E, Patel S, Cho H, Martel J, et al. (2014) Retrotaxis of human neutrophils during mechanical confinement inside microfluidic channels. IntegrBiol(Camb) 6:175–183.
    1. Irimia D (2010) Microfluidic technologies for temporal perturbations of chemotaxis. Annu Rev Biomed Eng 12:259–284.
    1. Anand D, Das S, Bhargava S, Srivastava LM, Garg A, et al.. (2014) Procalcitonin as a rapid diagnostic biomarker to differentiate between culture-negative bacterial sepsis and systemic inflammatory response syndrome: A prospective, observational, cohort study. J Crit Care.
    1. Fan H, Zhao Y, Zhu JH, Song FC (2014) Urine neutrophil gelatinase-associated lipocalin in septic patients with and without acute kidney injury. Ren Fail 36:1399–1403.
    1. Heit B, Robbins SM, Downey CM, Guan Z, Colarusso P, et al. (2008) PTEN functions to 'prioritize' chemotactic cues and prevent 'distraction' in migrating neutrophils. NatImmunol 9:743–752.
    1. Zhang Q, Raoof M, Chen Y, Sumi Y, Sursal T, et al. (2010) Circulating mitochondrial DAMPs cause inflammatory responses to injury. Nature 464:104–107.
    1. Kolaczkowska E, Kubes P (2013) Neutrophil recruitment and function in health and inflammation. NatRevImmunol 13:159–175.
    1. Harbarth S, Holeckova K, Froidevaux C, Pittet D, Ricou B, et al. (2001) Diagnostic value of procalcitonin, interleukin-6, and interleukin-8 in critically ill patients admitted with suspected sepsis. AmJRespirCrit Care Med 164:396–402.
    1. Calandra T, Echtenacher B, Roy DL, Pugin J, Metz CN, et al. (2000) Protection from septic shock by neutralization of macrophage migration inhibitory factor. NatMed 6:164–170.
    1. Kuster H, Weiss M, Willeitner AE, Detlefsen S, Jeremias I, et al. (1998) Interleukin-1 receptor antagonist and interleukin-6 for early diagnosis of neonatal sepsis 2 days before clinical manifestation. Lancet 352:1271–1277.
    1. Martensson J, Bell M, Oldner A, Xu S, Venge P, et al. (2010) Neutrophil gelatinase-associated lipocalin in adult septic patients with and without acute kidney injury. Intensive Care Med 36:1333–1340.
    1. Yali G, Jing C, Chunjiang L, Cheng Z, Xiaoqiang L, et al. (2014) Comparison of pathogens and antibiotic resistance of burn patients in the burn ICU or in the common burn ward. Burns 40:402–407.

Source: PubMed

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