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Erschienen in: Seminars in Immunopathology 6/2017

02.11.2017 | Review

Newborn susceptibility to infection vs. disease depends on complex in vivo interactions of host and pathogen

verfasst von: Byron Brook, Danny Harbeson, Rym Ben-Othman, Dorothee Viemann, Tobias R. Kollmann

Erschienen in: Seminars in Immunopathology | Ausgabe 6/2017

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Abstract

The burden of newborn infectious disease has long been recognized as the highest across the entire human life span. The precise underlying cause is unfortunately still far from clear. A substantial body of data derived mostly from in vitro experimentation indicates “lower” host immune responses in early vs. adult life and is briefly summarized within this review. However, emerging data derived mostly from in vivo experimentation reveal that the newborn host also exhibits an exuberant immune and inflammatory response following infection when compared to the adult. In this context, it is important to emphasize that “infection” does not equate “infectious disease,” as for many infections it is the host response to the infection that causes disease. This simple insight readily arranges existing evidence into cause-effect relationships that explain much of the increase in clinical suffering from infection in early life. We here briefly summarize the evidence in support of this paradigm and highlight the important implications it has for efforts to ameliorate the suffering and dying from infection in early life.
Literatur
2.
Zurück zum Zitat Soares MP, Teixeira L, Moita LF (2017) Disease tolerance and immunity in host protection against infection. Nature reviews 17:83–96PubMed Soares MP, Teixeira L, Moita LF (2017) Disease tolerance and immunity in host protection against infection. Nature reviews 17:83–96PubMed
3.
Zurück zum Zitat Liu L et al (2012) Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet 379:2151–2161CrossRefPubMed Liu L et al (2012) Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet 379:2151–2161CrossRefPubMed
4.
Zurück zum Zitat Shane AL, Sanchez PJ, Stoll BJ (2017) Neonatal sepsis. Lancet Shane AL, Sanchez PJ, Stoll BJ (2017) Neonatal sepsis. Lancet
6.
Zurück zum Zitat Cantey JB, Wozniak PS, Sanchez PJ (2015) Prospective surveillance of antibiotic use in the neonatal intensive care unit: results from the SCOUT study. Pediatr Infect Dis J 34:267–272CrossRefPubMed Cantey JB, Wozniak PS, Sanchez PJ (2015) Prospective surveillance of antibiotic use in the neonatal intensive care unit: results from the SCOUT study. Pediatr Infect Dis J 34:267–272CrossRefPubMed
8.
Zurück zum Zitat Kollmann TR, Kampmann B, Mazmanian SK, Marchant A, Levy O (2017) Protecting the newborn and young infant from infectious diseases: lessons from immune ontogeny. Immunity 46:350–363CrossRefPubMed Kollmann TR, Kampmann B, Mazmanian SK, Marchant A, Levy O (2017) Protecting the newborn and young infant from infectious diseases: lessons from immune ontogeny. Immunity 46:350–363CrossRefPubMed
9.
Zurück zum Zitat Zhang X, Zhivaki D, Lo-Man R (2017) Unique aspects of the perinatal immune system. Nature reviews Zhang X, Zhivaki D, Lo-Man R (2017) Unique aspects of the perinatal immune system. Nature reviews
10.
Zurück zum Zitat Ulas T et al (2017) S100-alarmin-induced innate immune programming protects newborn infants from sepsis. Nat Immunol 18:622–632CrossRefPubMed Ulas T et al (2017) S100-alarmin-induced innate immune programming protects newborn infants from sepsis. Nat Immunol 18:622–632CrossRefPubMed
11.
Zurück zum Zitat Wynn JL, Neu J, Moldawer LL, Levy O (2009) Potential of immunomodulatory agents for prevention and treatment of neonatal sepsis. J Perinatol: official journal of the California Perinatal Association 29:79–88CrossRef Wynn JL, Neu J, Moldawer LL, Levy O (2009) Potential of immunomodulatory agents for prevention and treatment of neonatal sepsis. J Perinatol: official journal of the California Perinatal Association 29:79–88CrossRef
12.
13.
14.
Zurück zum Zitat Lewis DB et al (2006) Newborn immunology: relevance to the clinician. Current Problems in Pediatric and Adolescent Health Care 36:189–204CrossRefPubMed Lewis DB et al (2006) Newborn immunology: relevance to the clinician. Current Problems in Pediatric and Adolescent Health Care 36:189–204CrossRefPubMed
16.
Zurück zum Zitat Wang G et al (2010) “Default” generation of neonatal regulatory T cells. J Immunol 185:71–78CrossRefPubMed Wang G et al (2010) “Default” generation of neonatal regulatory T cells. J Immunol 185:71–78CrossRefPubMed
17.
18.
Zurück zum Zitat Echeverry A, Saijo S, Schesser K, Adkins B (2010) Yersinia enterocolitica promotes robust mucosal inflammatory T cell immunity in murine neonates. Infect Immun 78:3595–3608CrossRefPubMedPubMedCentral Echeverry A, Saijo S, Schesser K, Adkins B (2010) Yersinia enterocolitica promotes robust mucosal inflammatory T cell immunity in murine neonates. Infect Immun 78:3595–3608CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Evans IA, Jones CA (2005) HSV induces an early primary Th1 CD4 T cell response in neonatal mice, but reduced CTL activity at the time of the peak adult response. Eur J Immunol 35:1454–1462CrossRefPubMed Evans IA, Jones CA (2005) HSV induces an early primary Th1 CD4 T cell response in neonatal mice, but reduced CTL activity at the time of the peak adult response. Eur J Immunol 35:1454–1462CrossRefPubMed
20.
Zurück zum Zitat Adkins B, Jones M, Bu Y, Levy RB (2004) Neonatal tolerance revisited again: specific CTL priming in mouse neonates exposed to small numbers of semi- or fully allogeneic spleen cells. Eur J Immunol 34:1901–1909CrossRefPubMed Adkins B, Jones M, Bu Y, Levy RB (2004) Neonatal tolerance revisited again: specific CTL priming in mouse neonates exposed to small numbers of semi- or fully allogeneic spleen cells. Eur J Immunol 34:1901–1909CrossRefPubMed
22.
Zurück zum Zitat Mascart F et al (2003) Bordetella pertussis infection in 2-month-old infants promotes type 1 T cell responses. J Immunol 170:1504–1509CrossRefPubMed Mascart F et al (2003) Bordetella pertussis infection in 2-month-old infants promotes type 1 T cell responses. J Immunol 170:1504–1509CrossRefPubMed
24.
Zurück zum Zitat Ota MO et al (2004) Hepatitis B immunisation induces higher antibody and memory Th2 responses in new-borns than in adults. Vaccine 22:511–519CrossRefPubMed Ota MO et al (2004) Hepatitis B immunisation induces higher antibody and memory Th2 responses in new-borns than in adults. Vaccine 22:511–519CrossRefPubMed
25.
Zurück zum Zitat Siegrist CA, Aspinall R (2009) B cell responses to vaccination at the extremes of age. Nature reviews 9:185–194PubMed Siegrist CA, Aspinall R (2009) B cell responses to vaccination at the extremes of age. Nature reviews 9:185–194PubMed
26.
Zurück zum Zitat Halsey N, Galazka A (1985) The efficacy of DPT and oral poliomyelitis immunization schedules initiated from birth to 12 weeks of age. Bull World Health Organ 63:1151–1169PubMedPubMedCentral Halsey N, Galazka A (1985) The efficacy of DPT and oral poliomyelitis immunization schedules initiated from birth to 12 weeks of age. Bull World Health Organ 63:1151–1169PubMedPubMedCentral
27.
Zurück zum Zitat Rodwell RL, Taylor KM, Tudehope DI, Gray PH (1993) Hematologic scoring system in early diagnosis of sepsis in neutropenic newborns. Pediatr Infect Dis J 12:372–376CrossRefPubMed Rodwell RL, Taylor KM, Tudehope DI, Gray PH (1993) Hematologic scoring system in early diagnosis of sepsis in neutropenic newborns. Pediatr Infect Dis J 12:372–376CrossRefPubMed
28.
Zurück zum Zitat Engle WA, McGuire WA, Schreiner RL, Yu PL (1988) Neutrophil storage pool depletion in neonates with sepsis and neutropenia. J Pediatr 113:747–749CrossRefPubMed Engle WA, McGuire WA, Schreiner RL, Yu PL (1988) Neutrophil storage pool depletion in neonates with sepsis and neutropenia. J Pediatr 113:747–749CrossRefPubMed
31.
Zurück zum Zitat Schelonka RL, Yoder BA, desJardins SE, Hall RB, Butler J (1994) Peripheral leukocyte count and leukocyte indexes in healthy newborn term infants. J Pediatr 125:603–606CrossRefPubMed Schelonka RL, Yoder BA, desJardins SE, Hall RB, Butler J (1994) Peripheral leukocyte count and leukocyte indexes in healthy newborn term infants. J Pediatr 125:603–606CrossRefPubMed
32.
Zurück zum Zitat Carr R (2000) Neutrophil production and function in newborn infants. Br J Haematol 110:18–28CrossRefPubMed Carr R (2000) Neutrophil production and function in newborn infants. Br J Haematol 110:18–28CrossRefPubMed
33.
Zurück zum Zitat Levy O et al (1999) Impaired innate immunity in the newborn: newborn neutrophils are deficient in bactericidal/permeability-increasing protein. Pediatrics 104:1327–1333CrossRefPubMed Levy O et al (1999) Impaired innate immunity in the newborn: newborn neutrophils are deficient in bactericidal/permeability-increasing protein. Pediatrics 104:1327–1333CrossRefPubMed
34.
Zurück zum Zitat Prosser A et al (2013) Phagocytosis of neonatal pathogens by peripheral blood neutrophils and monocytes from newborn preterm and term infants. Pediatr Res 74:503–510CrossRefPubMed Prosser A et al (2013) Phagocytosis of neonatal pathogens by peripheral blood neutrophils and monocytes from newborn preterm and term infants. Pediatr Res 74:503–510CrossRefPubMed
35.
Zurück zum Zitat Yost CC et al (2009) Impaired neutrophil extracellular trap (NET) formation: a novel innate immune deficiency of human neonates. Blood 113:6419–6427CrossRefPubMedPubMedCentral Yost CC et al (2009) Impaired neutrophil extracellular trap (NET) formation: a novel innate immune deficiency of human neonates. Blood 113:6419–6427CrossRefPubMedPubMedCentral
36.
Zurück zum Zitat Byrd AS et al (2016) NETosis in neonates: evidence of a reactive oxygen species-independent pathway in response to fungal challenge. J Infect Dis 213:634–639CrossRefPubMed Byrd AS et al (2016) NETosis in neonates: evidence of a reactive oxygen species-independent pathway in response to fungal challenge. J Infect Dis 213:634–639CrossRefPubMed
37.
Zurück zum Zitat Hallwirth U, Pomberger G, Pollak A, Roth E, Spittler A (2004) Monocyte switch in neonates: high phagocytic capacity and low HLA-DR expression in VLBWI are inverted during gestational aging. Pediatr Allergy Immunol 15:513–516CrossRefPubMed Hallwirth U, Pomberger G, Pollak A, Roth E, Spittler A (2004) Monocyte switch in neonates: high phagocytic capacity and low HLA-DR expression in VLBWI are inverted during gestational aging. Pediatr Allergy Immunol 15:513–516CrossRefPubMed
39.
Zurück zum Zitat Marodi L et al (1994) Candidacidal mechanisms in the human neonate. Impaired IFN-gamma activation of macrophages in newborn infants. J Immunol 153:5643–5649PubMed Marodi L et al (1994) Candidacidal mechanisms in the human neonate. Impaired IFN-gamma activation of macrophages in newborn infants. J Immunol 153:5643–5649PubMed
40.
Zurück zum Zitat Gille C, Spring B, Tewes L, Poets CF, Orlikowsky T (2006) A new method to quantify phagocytosis and intracellular degradation using green fluorescent protein-labeled Escherichia coli: comparison of cord blood macrophages and peripheral blood macrophages of healthy adults. Cytometry A 69:152–154CrossRefPubMed Gille C, Spring B, Tewes L, Poets CF, Orlikowsky T (2006) A new method to quantify phagocytosis and intracellular degradation using green fluorescent protein-labeled Escherichia coli: comparison of cord blood macrophages and peripheral blood macrophages of healthy adults. Cytometry A 69:152–154CrossRefPubMed
42.
Zurück zum Zitat Klein RB et al (1977) Decreased mononuclear and polymorphonuclear chemotaxis in human newborns, infants, and young children. Pediatrics 60:467–472PubMed Klein RB et al (1977) Decreased mononuclear and polymorphonuclear chemotaxis in human newborns, infants, and young children. Pediatrics 60:467–472PubMed
43.
Zurück zum Zitat Canaday DH et al (2006) Class II MHC antigen presentation defect in neonatal monocytes is not correlated with decreased MHC-II expression. Cell Immunol 243:96–106CrossRefPubMed Canaday DH et al (2006) Class II MHC antigen presentation defect in neonatal monocytes is not correlated with decreased MHC-II expression. Cell Immunol 243:96–106CrossRefPubMed
44.
Zurück zum Zitat Chheda S, Palkowetz KH, Garofalo R, Rassin DK, Goldman AS (1996) Decreased interleukin-10 production by neonatal monocytes and T cells: relationship to decreased production and expression of tumor necrosis factor-alpha and its receptors. Pediatr Res 40:475–483CrossRefPubMed Chheda S, Palkowetz KH, Garofalo R, Rassin DK, Goldman AS (1996) Decreased interleukin-10 production by neonatal monocytes and T cells: relationship to decreased production and expression of tumor necrosis factor-alpha and its receptors. Pediatr Res 40:475–483CrossRefPubMed
46.
Zurück zum Zitat Mathias B et al (2017) LPS stimulation of cord blood reveals a newborn-specific neutrophil transcriptomic response and cytokine production. Shock 47:606–614CrossRefPubMed Mathias B et al (2017) LPS stimulation of cord blood reveals a newborn-specific neutrophil transcriptomic response and cytokine production. Shock 47:606–614CrossRefPubMed
47.
Zurück zum Zitat Wynn JL et al (2008) Defective innate immunity predisposes murine neonates to poor sepsis outcome but is reversed by TLR agonists. Blood 112:1750–1758CrossRefPubMedPubMedCentral Wynn JL et al (2008) Defective innate immunity predisposes murine neonates to poor sepsis outcome but is reversed by TLR agonists. Blood 112:1750–1758CrossRefPubMedPubMedCentral
48.
Zurück zum Zitat Kollmann TR, Levy O, Montgomery RR, Goriely S (2012) Innate immune function by Toll-like receptors: distinct responses in newborns and the elderly. Immunity 37:771–783CrossRefPubMedPubMedCentral Kollmann TR, Levy O, Montgomery RR, Goriely S (2012) Innate immune function by Toll-like receptors: distinct responses in newborns and the elderly. Immunity 37:771–783CrossRefPubMedPubMedCentral
49.
50.
Zurück zum Zitat Angelone DF et al (2006) Innate immunity of the human newborn is polarized toward a high ratio of IL-6/TNF-α production in vitro and in vivo. Pediatr Res 60:205–209CrossRefPubMed Angelone DF et al (2006) Innate immunity of the human newborn is polarized toward a high ratio of IL-6/TNF-α production in vitro and in vivo. Pediatr Res 60:205–209CrossRefPubMed
51.
Zurück zum Zitat Wong OH, Huang F-P, Chiang AKS (2005) Differential responses of cord and adult blood-derived dendritic cells to dying cells. Immunology 116:13–20CrossRefPubMedPubMedCentral Wong OH, Huang F-P, Chiang AKS (2005) Differential responses of cord and adult blood-derived dendritic cells to dying cells. Immunology 116:13–20CrossRefPubMedPubMedCentral
52.
53.
Zurück zum Zitat Lee YC, Lin SJ (2013) Neonatal natural killer cell function: relevance to antiviral immune defense. Clinical & Developmental Immunology 2013:427696CrossRef Lee YC, Lin SJ (2013) Neonatal natural killer cell function: relevance to antiviral immune defense. Clinical & Developmental Immunology 2013:427696CrossRef
54.
Zurück zum Zitat Guilmot A, Hermann E, Braud VM, Carlier Y, Truyens C (2011) Natural killer cell responses to infections in early life. Journal of Innate Immunity 3:280–288CrossRefPubMed Guilmot A, Hermann E, Braud VM, Carlier Y, Truyens C (2011) Natural killer cell responses to infections in early life. Journal of Innate Immunity 3:280–288CrossRefPubMed
55.
Zurück zum Zitat D'Andrea A et al (2000) Neonatal invariant Valpha24+ NKT lymphocytes are activated memory cells. Eur J Immunol 30:1544–1550CrossRefPubMed D'Andrea A et al (2000) Neonatal invariant Valpha24+ NKT lymphocytes are activated memory cells. Eur J Immunol 30:1544–1550CrossRefPubMed
59.
Zurück zum Zitat Zhao J et al (2008) Hyper innate responses in neonates lead to increased morbidity and mortality after infection. Proc Natl Acad Sci U S A 105:7528–7533CrossRefPubMedPubMedCentral Zhao J et al (2008) Hyper innate responses in neonates lead to increased morbidity and mortality after infection. Proc Natl Acad Sci U S A 105:7528–7533CrossRefPubMedPubMedCentral
61.
Zurück zum Zitat Sugitharini V, Prema A, Berla Thangam E (2013) Inflammatory mediators of systemic inflammation in neonatal sepsis. Inflammation Research: Official Journal of the European Histamine Research Society 62:1025–1034CrossRef Sugitharini V, Prema A, Berla Thangam E (2013) Inflammatory mediators of systemic inflammation in neonatal sepsis. Inflammation Research: Official Journal of the European Histamine Research Society 62:1025–1034CrossRef
62.
Zurück zum Zitat Lines JL, Hoskins S, Hollifield M, Cauley LS, Garvy BA (2010) The migration of T cells in response to influenza virus is altered in neonatal mice. J Immunol 185:2980–2988CrossRefPubMedPubMedCentral Lines JL, Hoskins S, Hollifield M, Cauley LS, Garvy BA (2010) The migration of T cells in response to influenza virus is altered in neonatal mice. J Immunol 185:2980–2988CrossRefPubMedPubMedCentral
63.
64.
Zurück zum Zitat Byun H-J et al (2007) An evaluation of the neonatal immune system using a Listeria infection model. Neonatology 92:83–90CrossRefPubMed Byun H-J et al (2007) An evaluation of the neonatal immune system using a Listeria infection model. Neonatology 92:83–90CrossRefPubMed
65.
Zurück zum Zitat Kronforst KD et al (2012) A neonatal model of intravenous Staphylococcus epidermidis infection in mice < 24 h old enables characterization of early innate immune responses. PLoS One 7:e43897CrossRefPubMedPubMedCentral Kronforst KD et al (2012) A neonatal model of intravenous Staphylococcus epidermidis infection in mice < 24 h old enables characterization of early innate immune responses. PLoS One 7:e43897CrossRefPubMedPubMedCentral
66.
Zurück zum Zitat Black A, Bhaumik S, Kirkman RL, Weaver CT, Randolph DA (2012) Developmental regulation of Th17-cell capacity in human neonates. Eur J Immunol 42:311–319CrossRefPubMed Black A, Bhaumik S, Kirkman RL, Weaver CT, Randolph DA (2012) Developmental regulation of Th17-cell capacity in human neonates. Eur J Immunol 42:311–319CrossRefPubMed
67.
Zurück zum Zitat Seok J et al (2013) Genomic responses in mouse models poorly mimic human inflammatory diseases. Proc Natl Acad Sci U S A Seok J et al (2013) Genomic responses in mouse models poorly mimic human inflammatory diseases. Proc Natl Acad Sci U S A
68.
69.
Zurück zum Zitat Bianchi ME (2007) DAMPs, PAMPs and alarmins: all we need to know about danger. J Leukoc Biol 81:1–5CrossRefPubMed Bianchi ME (2007) DAMPs, PAMPs and alarmins: all we need to know about danger. J Leukoc Biol 81:1–5CrossRefPubMed
70.
Zurück zum Zitat Vogl T et al (2007) Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock. Nat Med 13:1042–1049CrossRefPubMed Vogl T et al (2007) Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock. Nat Med 13:1042–1049CrossRefPubMed
71.
Zurück zum Zitat Vogl T, Gharibyan AL, Morozova-Roche LA (2012) Pro-inflammatory S100A8 and S100A9 proteins: self-assembly into multifunctional native and amyloid complexes. Int J Mol Sci 13:2893–2917CrossRefPubMedPubMedCentral Vogl T, Gharibyan AL, Morozova-Roche LA (2012) Pro-inflammatory S100A8 and S100A9 proteins: self-assembly into multifunctional native and amyloid complexes. Int J Mol Sci 13:2893–2917CrossRefPubMedPubMedCentral
72.
Zurück zum Zitat Foell D, Frosch M, Sorg C, Roth J (2004) Phagocyte-specific calcium-binding S100 proteins as clinical laboratory markers of inflammation. Clinica chimica acta; international journal of clinical chemistry 344:37–51CrossRefPubMed Foell D, Frosch M, Sorg C, Roth J (2004) Phagocyte-specific calcium-binding S100 proteins as clinical laboratory markers of inflammation. Clinica chimica acta; international journal of clinical chemistry 344:37–51CrossRefPubMed
73.
Zurück zum Zitat Viemann D et al (2005) Myeloid-related proteins 8 and 14 induce a specific inflammatory response in human microvascular endothelial cells. Blood 105:2955–2962CrossRefPubMed Viemann D et al (2005) Myeloid-related proteins 8 and 14 induce a specific inflammatory response in human microvascular endothelial cells. Blood 105:2955–2962CrossRefPubMed
74.
Zurück zum Zitat Foell D, Wittkowski H, Vogl T, Roth J (2007) S100 proteins expressed in phagocytes: a novel group of damage-associated molecular pattern molecules. J Leukoc Biol 81:28–37CrossRefPubMed Foell D, Wittkowski H, Vogl T, Roth J (2007) S100 proteins expressed in phagocytes: a novel group of damage-associated molecular pattern molecules. J Leukoc Biol 81:28–37CrossRefPubMed
75.
Zurück zum Zitat Foell D, Wittkowski H, Roth J (2009) Monitoring disease activity by stool analyses: from occult blood to molecular markers of intestinal inflammation and damage. Gut 58:859–868CrossRefPubMed Foell D, Wittkowski H, Roth J (2009) Monitoring disease activity by stool analyses: from occult blood to molecular markers of intestinal inflammation and damage. Gut 58:859–868CrossRefPubMed
76.
Zurück zum Zitat Austermann J et al (2014) Alarmins MRP8 and MRP14 induce stress tolerance in phagocytes under sterile inflammatory conditions. Cell Rep 9:2112–2123CrossRefPubMed Austermann J et al (2014) Alarmins MRP8 and MRP14 induce stress tolerance in phagocytes under sterile inflammatory conditions. Cell Rep 9:2112–2123CrossRefPubMed
77.
Zurück zum Zitat West MA, Heagy W (2002) Endotoxin tolerance: a review. Crit Care Med 30:S64–S73CrossRef West MA, Heagy W (2002) Endotoxin tolerance: a review. Crit Care Med 30:S64–S73CrossRef
78.
Zurück zum Zitat Biswas SK, Lopez-Collazo E (2009) Endotoxin tolerance: new mechanisms, molecules and clinical significance. Trends Immunol 30:475–487CrossRefPubMed Biswas SK, Lopez-Collazo E (2009) Endotoxin tolerance: new mechanisms, molecules and clinical significance. Trends Immunol 30:475–487CrossRefPubMed
79.
Zurück zum Zitat Gomez-Lopez N, StLouis D, Lehr MA, Sanchez-Rodriguez EN, Arenas-Hernandez M (2014) Immune cells in term and preterm labor. Cellular & Molecular Immunology 11:571–581CrossRef Gomez-Lopez N, StLouis D, Lehr MA, Sanchez-Rodriguez EN, Arenas-Hernandez M (2014) Immune cells in term and preterm labor. Cellular & Molecular Immunology 11:571–581CrossRef
81.
Zurück zum Zitat Heinemann AS et al (2017) In neonates S100A8/S100A9 alarmins prevent the expansion of a specific inflammatory monocyte population promoting septic shock. FASEB J 31:1153–1164CrossRefPubMed Heinemann AS et al (2017) In neonates S100A8/S100A9 alarmins prevent the expansion of a specific inflammatory monocyte population promoting septic shock. FASEB J 31:1153–1164CrossRefPubMed
82.
Zurück zum Zitat Yamamoto M et al (2003) Role of adaptor TRIF in the MyD88-independent toll-like receptor signaling pathway. Science 301:640–643CrossRefPubMed Yamamoto M et al (2003) Role of adaptor TRIF in the MyD88-independent toll-like receptor signaling pathway. Science 301:640–643CrossRefPubMed
83.
Zurück zum Zitat Weighardt H et al (2006) Type I IFN modulates host defense and late hyperinflammation in septic peritonitis. J Immunol 177:5623–5630CrossRefPubMed Weighardt H et al (2006) Type I IFN modulates host defense and late hyperinflammation in septic peritonitis. J Immunol 177:5623–5630CrossRefPubMed
84.
Zurück zum Zitat Kanagavelu S et al (2015) TIR domain-containing adapter-inducing beta interferon (TRIF) mediates immunological memory against bacterial pathogens. Infect Immun 83:4404–4415CrossRefPubMedPubMedCentral Kanagavelu S et al (2015) TIR domain-containing adapter-inducing beta interferon (TRIF) mediates immunological memory against bacterial pathogens. Infect Immun 83:4404–4415CrossRefPubMedPubMedCentral
85.
Zurück zum Zitat Kolb JP, Casella CR, SenGupta S, Chilton PM, Mitchell TC (2014) Type I interferon signaling contributes to the bias that toll-like receptor 4 exhibits for signaling mediated by the adaptor protein TRIF. Sci Signal 7:ra108CrossRefPubMedPubMedCentral Kolb JP, Casella CR, SenGupta S, Chilton PM, Mitchell TC (2014) Type I interferon signaling contributes to the bias that toll-like receptor 4 exhibits for signaling mediated by the adaptor protein TRIF. Sci Signal 7:ra108CrossRefPubMedPubMedCentral
86.
Zurück zum Zitat Wynn JL et al (2015) Postnatal age is a critical determinant of the neonatal host response to sepsis. Molecular Medicine (Cambridge, Mass) 21:496–504 Wynn JL et al (2015) Postnatal age is a critical determinant of the neonatal host response to sepsis. Molecular Medicine (Cambridge, Mass) 21:496–504
87.
Zurück zum Zitat Vogl T, Leukert N, Barczyk K, Strupat K, Roth J (2006) Biophysical characterization of S100A8 and S100A9 in the absence and presence of bivalent cations. Biochim Biophys Acta 1763:1298–1306CrossRefPubMed Vogl T, Leukert N, Barczyk K, Strupat K, Roth J (2006) Biophysical characterization of S100A8 and S100A9 in the absence and presence of bivalent cations. Biochim Biophys Acta 1763:1298–1306CrossRefPubMed
88.
Zurück zum Zitat Austermann J, Zenker S, Roth J (2017) S100-alarmins: potential therapeutic targets for arthritis. Expert Opin Ther Targets 21:739–751CrossRefPubMed Austermann J, Zenker S, Roth J (2017) S100-alarmins: potential therapeutic targets for arthritis. Expert Opin Ther Targets 21:739–751CrossRefPubMed
89.
Zurück zum Zitat Tanimura N et al (2014) The attenuated inflammation of MPL is due to the lack of CD14-dependent tight dimerization of the TLR4/MD2 complex at the plasma membrane. Int Immunol 26:307–314CrossRefPubMed Tanimura N et al (2014) The attenuated inflammation of MPL is due to the lack of CD14-dependent tight dimerization of the TLR4/MD2 complex at the plasma membrane. Int Immunol 26:307–314CrossRefPubMed
91.
Zurück zum Zitat Amenyogbe N, Kollmann TR, Ben-Othman R (2017) Early-life host-microbiome interphase: the key frontier for immune development. Frontiers in pediatrics 5:111CrossRefPubMedPubMedCentral Amenyogbe N, Kollmann TR, Ben-Othman R (2017) Early-life host-microbiome interphase: the key frontier for immune development. Frontiers in pediatrics 5:111CrossRefPubMedPubMedCentral
92.
93.
95.
Zurück zum Zitat Underwood MA (2017) Impact of probiotics on necrotizing enterocolitis. Semin Perinatol 41:41–51CrossRefPubMed Underwood MA (2017) Impact of probiotics on necrotizing enterocolitis. Semin Perinatol 41:41–51CrossRefPubMed
96.
Zurück zum Zitat Panigrahi P et al (2017) A randomized synbiotic trial to prevent sepsis among infants in rural India. Nature Panigrahi P et al (2017) A randomized synbiotic trial to prevent sepsis among infants in rural India. Nature
98.
Zurück zum Zitat Nino DF, Sodhi CP, Hackam DJ (2016) Necrotizing enterocolitis: new insights into pathogenesis and mechanisms. Nat Rev Gastroenterol Hepatol 13:590–600CrossRefPubMedPubMedCentral Nino DF, Sodhi CP, Hackam DJ (2016) Necrotizing enterocolitis: new insights into pathogenesis and mechanisms. Nat Rev Gastroenterol Hepatol 13:590–600CrossRefPubMedPubMedCentral
99.
Zurück zum Zitat Adkins B, Leclerc C, Marshall-Clarke S (2004) Neonatal adaptive immunity comes of age. Nature Reviews 4:553–564PubMed Adkins B, Leclerc C, Marshall-Clarke S (2004) Neonatal adaptive immunity comes of age. Nature Reviews 4:553–564PubMed
101.
102.
Zurück zum Zitat Lee S et al (2013) Genetic determinants for cadmium and arsenic resistance among Listeria monocytogenes serotype 4b isolates from sporadic human listeriosis patients. Appl Environ Microbiol 79:2471–2476CrossRefPubMedPubMedCentral Lee S et al (2013) Genetic determinants for cadmium and arsenic resistance among Listeria monocytogenes serotype 4b isolates from sporadic human listeriosis patients. Appl Environ Microbiol 79:2471–2476CrossRefPubMedPubMedCentral
Metadaten
Titel
Newborn susceptibility to infection vs. disease depends on complex in vivo interactions of host and pathogen
verfasst von
Byron Brook
Danny Harbeson
Rym Ben-Othman
Dorothee Viemann
Tobias R. Kollmann
Publikationsdatum
02.11.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Seminars in Immunopathology / Ausgabe 6/2017
Print ISSN: 1863-2297
Elektronische ISSN: 1863-2300
DOI
https://doi.org/10.1007/s00281-017-0651-z

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