Am J Perinatol 2000; Volume 17(Number 02): 107-112
DOI: 10.1055/s-2000-9507
Copyright © 2000 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

NEUTROPHIL CHEMOTAXIS AND RANDOM MIGRATION IN PRETERM AND TERM INFANTS WITH SEPSIS

Münevver Türkmen1,4 , Mehmet Satar2 , Aytug Atici3,4
  • 1Department of Pediatrics, Adnan Menderes University Medical Faculty, Neonatal Intensive Care Unit, Aydin, Turkey
  • 2Department of Pediatrics, Çukurova University Medical Faculty, Neonatal Intensive Care Unit, Adana, Turkey
  • 3Department of Pediatrics, Seyhan Hospital, Adana, Turkey; Formerly at Çukurova University.
Further Information

Publication History

Publication Date:
31 December 2000 (online)

ABSTRACT

The aim of this study was to evaluate neutrophil chemotaxis and random migration in healthy newborn infants and septic neonates with similar gestational and postnatal age. Possible relationships between chemotactic activity, random migration, causative microorganisms, and clinical course of septic infants were also investigated. The neutrophil chemotaxis and random migration was evaluated in 24 healthy newborn babies and 34 septic neonates and 20 healthy adults by modified Boyden technique. The mean neutrophil chemotaxis of healthy preterm-term infants and adults were similar (66.6 ± 18.9, 64.4 ± 19.9, and 74.7 ± 17 μm, respectively). The mean neutrophil random migration of healthy term infants was not different than that of adults. But the mean neutrophil random migration of healthy preterm infants was lower than that of adults (36.9 ± 13.7 and 43.5 ± 11.8 μm, respectively) (p = 0.03). The mean neutrophil chemotaxis and random migration septic term infants were not different from the value of healthy term infants (p > 0.05). Although the mean random migration of septic and preterm infants were similar (p > 0.05), the mean neutrophil chemotaxis of septic preterm infants was lower than the value of healthy preterm infants (p = 0.04). Not only mean neutrophil chemotaxis of septic preterm and term infants were significantly lower than that of adults (p = 0.002 and p = 0.006, respectively), but also neutrophil random migration of septic preterm and term infants were significantly lower than that of adults (p = 0.001 and p = 0.005, respectively). There was no relationship between the nature of causative microorganism and neutrophil random migration or chemotactic activity. Polymorphonuclear leukocytes chemotaxis was significantly lower in preterm with sepsis compared with healthy preterm-term infants and adults. These findings may indicate deterioration in neutrophil functions in premature babies under stress but more detailed studies with larger groups are needed.

REFERENCES

  • 1 Gorlin J B, Stossel T P. The phagocytic system: structure and function. In: Nathan DG, Oski FA, eds. Hematology of Infancy and Childhood, Vol 1, 4th ed. Philadelphia: WB Saunders 1993: 882-977
  • 2 Carr R, Pumford D, Davies J M. Neutrophil chemotaxis and adhesion in preterm babies.  Arch Dis Child . 1992;  67 813-817
  • 3 Sacci F, Rondini G, Mingrat G. Different maturation of neutrophil chemotaxis in term and preterm newborn infants.  Pediatrics . 1982;  20 273-274
  • 4 Usmani S S, Schlessel S J, Sia G C, Kamran S, Orner D S. Polymorphonuclear leukocyte function in the preterit neonate: effect of chronologic age.  Pediatrics . 1991;  87 675-679
  • 5 Krause J P, Herson V C, Boutin-Lebowitz J. Polymorphonuclear leukocyte adherence and chemotaxis in stressed and healthy neonates.  Pediatr Res . 1986;  20 296-300
  • 6 Anderson D C, Hughes J B, Edwards M S, Buffone G J, Baker C J. Impaired chemotaxigenesis by type III Group B Streptococci in neonatal sera: relationship to diminished concentration of specific anticapsular antibody and abnormalities of serum complement.  Pediatr Res . 1983;  17 496-502
  • 7 Miller E M. Chemotactic function in the human neonate: humoral and cellular aspects.  Pediatr Res . 1971;  5 487-492
  • 8 Klein B R, Fischer T J, Gard S E, Biberstein M, Rich C K, Stiehm R E. Decreased mononuclear and polymorphonuclear chemotaxis in human newborn, infants, and young children.  Pediatrics . 1977;  60 467-472
  • 9 Anderson D C, Hughes B J, Smith C W. Abnormal mobility of neonatal polymorphonuclear leukocytes: relationship to impaired redistribution of surface adhesion sites by chemotactic factor or colchicine.  Clin Invest . 1981;  68 863-874
  • 10 Eisenfeld L, Krause P J, Herson V. Longitudinal study of neutrophil adherence and motility.  Pediatrics . 1990;  117 926-929
  • 11 Bektas S, Goetze B, Speer C P. Decreased adherence, chemotaxis and phagocytic activities of neutrophils from preterm neonates.  Acta Pediatr Scand . 1990;  79 1031-1038
  • 12 Boyum A. Isolation of mononuclear cell and granulocytes from human blood: isolation of mononuclear cells by one centrifugation and of granulocytes by combining centrifugation and sedimentation at 1 g.  Scand J Clin Lab Invest . 1968;  97(suppl) 77-91
  • 13 Boyden S V. The chemotactic effect mixtures of antibody and antigen on polymorphonuclear leucocytes.  J Exp Med . 1962;  115 453
  • 14 Lewis D B, Wilson C B. Developmental immunology and role of host defenses in neonatal susceptibility to infection. In: Remington JS, Klein JO, eds. Infectious Diseases of the Fetus and Newborn Infant, 4th ed Philadelphia: W.B. Saunders 1995: 20-98
  • 15 Tono-Oka T, Nakayama M, Uehara H. Characteristics of impaired chemotactic function in cord blood leucocytes.  Pediatr Res . 1979;  13 148-151
  • 16 Althaus D, Keller H U, Hess M W, Cottier H. Impaired neutrophil locomotion during acute bacterial infection.  Int Arch Allerg Appl Immunol . 1980;  61 321-328
  • 17 Laurenti F, Ferro R, Marzetti G, Rossini M, Bucci G. Neutrophil chemotaxis in preterm infants with infections.  Pediatrics . 1980;  30 468-470
  • 18 Chabior M. Cellular and humoral components of neutrophil chemotaxis in neonates with bacterial infection.  Mater Med Pol . 1994;  26 49-53
  • 19 McCall C E, Caves J, Cooper R, DeChatelet L. Functional characteristics of human toxic neutrophils.  J Infect Dis . 1971;  124 68-75
    >