Alterations in neonatal neutrophil function attributable to increased immature forms

Early Human Development

Volumn 103, Issue , 2016, Pages 1-7

  Makoni, Marjorie ^a   Eckert, Jeffrey ^a   Anne Pereira, H ^b   Nizet, Victor ^c   Lawrence, Shelley M ^a,c  

^a UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF OKLAHOMA HEALTH SCIENCES CENTER   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD11B ANTIGEN; CD16 ANTIGEN; CD45 ANTIGEN; CHEMOKINE; CYTOKINE; FORMYLMETHIONYLLEUCYLPHENYLALANINE; GREEN FLUORESCENT PROTEIN; LEUKOCYTE ANTIGEN;

ARTICLE; CELL MATURATION; CESAREAN SECTION; CONTROLLED STUDY; ESCHERICHIA COLI; FLOW CYTOMETRY; GENE EXPRESSION; GRANULOCYTE; HUMAN; IMMUNOASSAY; LABOR; METAMYELOCYTE; MYELOCYTE; NEUTROPHIL; NEUTROPHIL CHEMOTAXIS; NEWBORN; PHAGOCYTOSIS; PROMYELOCYTE; PROTEIN EXPRESSION; UMBILICAL CORD BLOOD; VAGINAL DELIVERY; VEIN PUNCTURE; ADULT; BLOOD; CELL DIFFERENTIATION; CHEMOTAXIS; CYTOLOGY; FEMALE; GENETICS; IMMUNOLOGY; MALE; METABOLISM; PHYSIOLOGY;

ADULT; ANTIGENS, CD; CELL DIFFERENTIATION; CHEMOTAXIS; CYTOKINES; FEMALE; HUMANS; INFANT, NEWBORN; MALE; NEUTROPHILS; PHAGOCYTOSIS;

EID: 84978795141     PISSN: 03783782     EISSN: 18726232     Source Type: Journal    
DOI: 10.1016/j.earlhumdev.2016.05.016     Document Type: Article

References (52)

1. [1] Carr, R., Neutrophil production and function in newborn infants. Br. J. Haematol. 110:1 (Jul 2000), 18–28.
2. [2] Al-Hadithy, H., Addison, I.E., Goldstone, A.H., Cawley, J.C., Shaw, J.C., Defective neutrophil function in low-birth-weight, premature infants. J. Clin. Pathol. 34:4 (Apr 1981), 366–370.
3. [3] Carr, R., The role of colony stimulating factors and immunoglobulin in the prevention and treatment of neonatal infection. Arch. Dis. Child. Fetal Neonatal Ed. 98:3 (May 2013), F192–F194.
4. [4] Klebanoff, S.J., Waltersdorph, A.M., Prooxidant activity of transferrin and lactoferrin. J. Exp. Med. 172:5 (Nov 1 1990), 1293–1303.
5. [5] Urlichs, F., Speer, C.P., Neutrophil function in preterm and term infants. NeoReviews 5:10 (Oct 2004), e417–e429.
6. [6] Kim, S.K., Keeney, S.E., Alpard, S.K., Schmalstieg, F.C., Comparison of L-selectin and CD11b on neutrophils of adults and neonates during the first month of life. Pediatr. Res. 53:1 (Jan 2003), 132–136.
7. [7] Nussbaum, C., Sperandio, M., Innate immune cell recruitment in the fetus and neonate. J. Reprod. Immunol. 90:1 (Jun 2011), 74–81.
8. [8] McEvoy, L.T., Zakem-Cloud, H., Tosi, M.F., Total cell content of CR3 (CD11b | CD18) and LFA-1(CD11a | CD18) in neonatal neutrophils: relationship to gestational age. Blood 87:9 (May 1 1996), 3929–3933.
9. [9] Speer, C.P., Johnston, R.B. Jr., Neutrophil function in newborn infants. Pollin, R.A., Fox, W.W., (eds.) Fetal and Neonatal Physiology, 1998, WB Saunders, Philadelphia, PA, 1954–1960.
10. [10] Taniuchi, S., Kinoshita, Y., Yamamoto, A., Fujiwara, T., Hattori, K., Hasui, M., Kobayashi, Y., Heterogeneity in F-actin polymerization of cord blood polymorphonuclear leukocytes stimulated with FMLP. Pediatr. Int. 41:1 (Feb 1999), 37–41.
11. [11] Weinberger, B., Laskin, D.L., Mariano, T.M., Sunil, V.R., DeCoste, C.J., Heck, D.E., Gardner, C.R., Laskin, J.D., Mechanisms underlying reduced responsiveness of neonatal neutrophils to distinct chemoattractants. J. Leukoc. Biol. 70:6 (Dec 2001), 969–976.
12. [12] Eisenfeld, L., Krause, P.J., Herson, V., Savidakis, J., Bannon, P., Maderazo, E., Woronick, C., Giuliano, C., Banco, L., Longitudinal study of neutrophil adherence and motility. J. Pediatr. 117:6 (Dec 1990), 926–929.
13. [13] Carr, R., Pumford, D., Davies, J.M., Neutrophil chemotaxis and adhesion in preterm babies. Arch. Dis. Child. 67:7 Spec No (1992 Jul), 813–817.
14. [14] Schmutz, N., Henry, E., Jopling, J., Christensen, R.D., Expected ranges for blood neutrophil concentrations of neonates: the Manroe and Mouzinho charts revisited. J. Perinatol. 28:4 (Apr 2008), 275–281.
15. [15] Lawrence, S.M., Eckert, J., Makoni, M., Pereira, H.A., Is the use of complete blood counts with manual differentials for determining neutrophil composition in newborns antiquated?. Ann. Clin. Lab. Sci. 45:4 (2015), 403–413.
16. [16] Boner, A., Zeligs, B.J., Bellanti, J.A., Chemotactic responses of various differential stages of neutrophils from human cord and adult blood. Infect. Immun. 35:3 (Mar 1982), 921–928.
17. [17] Pham, T.N., Neutrophil serine proteases: specific regulators of inflammation. Nat. Rev. Immunol. 6:7 (Jul 2006), 541–550.
18. [18] Gullberg, U., Bengtsson, N., Bülow, E., Garwicz, D., Lindmark, A., Olsson, I., Processing and targeting of granule proteins in human neutrophils. J. Immunol. Methods 232:1–2 (Dec 17 1999), 201–210.
19. [19] Gullberg, U., Andersson, E., Garwicz, D., Lindmark, A., Olsson, I., Biosynthesis, processing and sorting of neutrophil proteins: insight into neutrophil granule development. Eur. J. Haematol. 58 (1997), 137–153.
20. [20] Borregaard, N., Sørensen, O.E., Theilgaard-Mönch, K., Neutrophil granules: a library of innate proteins. Trends Immunol. 28:8 (Aug 2007), 340–345.
21. [21] Boström, E.A., Tarkowski, A., Bokarewa, M., Resistin is stored in neutrophil granules being released upon challenge with inflammatory stimuli. Biochim. Biophys. Acta 1793:12 (Dec 2009), 1894–1900.
22. [22] Robinson, J.P., Carter, W.O., Narayanan, P., Functional assays by flow cytometry. Rose, N.R., de Marcario, E., Folds, J.D., Lane, H.C., Nakurmura, R., (eds.) Manual of Clinical and Laboratory Immunology, 1997, American Society of Microbiology Press, Washington, D.C., USA, 245–254.
23. [23] Edwards, S.W., Biochemistry and Physiology of the Neutrophil. first ed., 1994, Cambridge University Press Publishing, New York.
24. [24] Fox, S.E., Lu, W., Maheshwari, A., Christensen, R.D., Calhoun, D.A., The effects and comparative differences of neutrophil specific chemokines on neutrophil chemotaxis of the neonate. Cytokine 29:3 (Feb 7 2005), 135–140.
25. [25] Sacchi, F., Rondini, G., Mingrat, G., Stronati, M., Gancia, G.P., Marseglia, G.L., Siccardi, A.G., Different maturation of neutrophil chemotaxis in term and preterm newborn infants. J. Pediatr. 101:2 (Aug 1982), 273–274.
26. [26] Hilmo, A., Howard, T.H., F-actin content of neonate and adult neutrophils. Blood 69:3 (March 1987), 945–949.
27. [27] Abughali, N., Berger, M., Tosi, M.F., Deficient total cell content of CR3 (CD11b) in neonatal neutrophils. Blood 83:4 (Feb 1994), 1086–1092.
28. [28] Ferguson, E., Etzell, J.E., To and fro on band count reporting and clinical utility. Q&A, CAP Today, November 2010.
29. [29] Clinical and Laboratory Standards Institute (CLSI), Reference Leukocyte (WBC) Differential Count (Proportional) and Evaluation of Instrumental Methods: Approved Standard. second ed., 2007.
30. [30] Cornbleet, P.J., Novak, R.W., Classifying segmented and band neutrophils: interlaboratory variability leads to a combining of the proficiency testing categories. CAP Today, May 1994, 38–41.
31. [31] Krause, P.J., Kreutzer, D.L., Eisenfeld, L., Herson, V.C., Weisman, S., Bannon, P., Greca, N., Characterization of nonmotile neutrophil subpopulations in neonates and adults. Pediatr. Res. 25:5 (May 1989), 519–524.
32. [32] Yegin, O., Chemotaxis in childhood. Pediatr. Res. 17:3 (1983), 183–187.
33. [33] Krause, P.J., Herson, V.C., Boutin-Lebowitz, J., Eisenfeld, L., Block, C., LoBello, T., Maderazo, E.G., Polymorphonuclear leukocyte adherence and chemotaxis in stressed and healthy neonates. Pediatr. Res. 20:4 (Apr 1986), 296–300.
34. [34] Repo, H., Jokipii, A.M., Leirisalo, M., Kosunen, T.U., Leucocyte motility in the newborn: determination of spontaneous movement is essential in the in vitro assessment of neutrophil chemotaxis. Clin. Exp. Immunol. 40:3 (Jun 1980), 620–626.
35. [35] Filias, A., Theodorou, G.L., Mouzopoulou, S., Varvarigou, A.A., Mantagos, S., Karakantza, M., Phagocytic ability of neutrophils and monocytes in neonates. BMC Pediatr., 11, Apr 14 2011, 29.
36. [36] Dossett, J.H., Williams, R.C. Jr., Quie, P.G., Studies on interaction of bacteria, serum factors and polymorphonuclear leukocytes in mothers and newborns. Pediatrics 44:1 (Jul 1969), 49–57.
37. [37] Mendelson, C.R., Minireview fetal-maternal hormonal signaling in pregnancy and labor. Mol. Endocrinol. 23:7 (July 2009), 947–954.
38. [38] Imanirad, P., Dzierzak, E., Hypoxia and HIFs in regulating the development of the hematopoietic system. Blood Cells Mol. Dis. 51:4 (Dec 2013), 256–263.
39. [39] Murphy, P.J., The fetal circulation. BJA Education Pain 5:4 (November 2005), 107–112.
40. [40] Vorherr, H., Placental insufficiency in relation to postterm pregnancy and fetal postmaturity. Evaluation of fetoplacental function; management of the postterm gravida. Am. J. Obstet. Gynecol. 123:1 (Sep 1 1975), 67–103.
41. [41] Ahmed, A.I., Versi, E., Prolonged pregnancy. Curr. Opin. Obstet. Gynecol. 5:5 (Oct 1993), 669–674.
42. [42] Freeman, R.K., LaGrew, D.C., Prolonged pregnancy. Gabbe, S.G., Niebyl, J.R., Simpson, J.L., (eds.) Obstetrics: Normal and Problem Pregnancies, second ed., 1991, Churchill Livingstone, New York, 945–956.
43. [43] Bhandari, T., Nizet, V., Hypoxia-inducible factor (HIF) as a pharmacological target for prevention and treatment of infectious diseases. Infect. Dis. Ther., 24, Jun 2014.
44. [44] Dehne, N., Brüne, B., HIF-1 in the inflammatory microenvironment. Exp. Cell Res. 315:11 (Jul 1 2009), 1791–1797.
45. [45] Vancurova, I., Bellani, P., Davidson, D., Activation of nuclear factor-kappaB and its suppression by dexamethasone in polymorphonuclear leukocytes: newborn versus adult. Pediatr. Res. 49:2 (Feb 2001), 257–262.
46. [46] McDonald, P.P., Bald, A., Cassatella, M.A., Activation of the NF-kappaB pathway by inflammatory stimuli in human neutrophils. Blood 89:9 (May 1 1997), 3421–3433.
47. [47] Cramer, T., Yamanishi, Y., Clausen, B.E., Forster, I., Pawlinski, R., Mackman, N., Haase, V.H., Jaenisch, R., Corr, M., Nizet, V., Firestein, G.S., Gerber, H.P., Ferrara, N., Johnson, R.S., HIF-1a is essential for myeloid cell-mediated inflammation. Cell 112 (2003), 645–657.
48. [48] Karhausen, J., Haase, V.H., Colgan, S.P., Inflammatory hypoxia: role of hypoxia-inducible factor. Cell Cycle 4:2 (Feb 2005), 256–258.
49. [49] Levy, O., Innate immunity of the newborn: basic mechanisms and clinical correlates. Nat. Rev. Immunol. 7:5 (May 2007), 379–390.
50. [50] Nussbaum, C., Gloning, A., Pruenster, M., Frommhold, D., Bierschenk, S., Genzel-Boroviczéy, O., von Andrian, U.H., Quackenbush, E., Sperandio, M., Neutrophil and endothelial adhesive function during human fetal ontogeny. J. Leukoc. Biol. 93:2 (Feb 2013), 175–184.
51. [51] Urlichs, F., Speer, C.P., Neutrophil function in preterm and term infants. NeoReviews 5 (2004), e417–e430.
52. [52] Birle, A., Nebe, C.T., Hill, S., Hartmann, K., Poeschl, J., Koch, L., Neutrophil chemotaxis in cord blood of term and preterm neonates is reduced in preterm neonates and influenced by the mode of delivery and anaesthesia. PLoS One, 10(4), Apr 13 2015 e0120341.