z-logo
open-access-imgOpen Access
Mode of delivery directs the phagocyte functions of infants for the first 6 months of life
Author(s) -
MinnaMaija Grönlund,
Jari Nuutila,
Leea Pelto,
EsaMatti Lilius,
Erika Isolauri,
Seppo Salminen,
Pentti Kero,
O-P Lehtonen
Publication year - 1999
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1999.00902.x
Subject(s) - phagocyte , phagocytosis , immunology , cd16 , immune system , cd64 , receptor , receptor expression , integrin alpha m , cord blood , biology , medicine , antigen , cd3 , cd8
Factors that direct the immune responsiveness of the newborn beyond the immediate post‐natal period are not known. We investigated the influence of mode of delivery and type of feeding on the phagocyte activity during the first 6 months of life. Sixty‐four healthy infants (34 delivered vaginally and 30 by elective Caesarean section) were studied at birth and at the ages of 2 and 6 months. Phagocyte functions were studied by measuring the chemiluminescence (CL) activity of whole blood and isolated leucocytes and by investigating the expression of phagocyte receptors (FcγRI (CD64), FcγRII (CD32), FcγRIII (CD16), CR1 (CD35), CR3 (CD11b) and FcαR (CD89)) on neutrophils, monocytes and eosinophils by using receptor‐specific MoAbs and immunofluorescence flow cytometry. Infants born by elective Caesarean section had significantly higher CL activity than those delivered vaginally during the entire 6‐month follow up. In addition, infants who received formula feeds had significantly higher CL activity at 6 months of age and higher expression of FcγRI‐, Fcα‐ and CR3‐receptors on neutrophils than infants exclusively breast‐fed. We suggest that stress reaction associated with labour influences the phagocytic activity measured in the cord blood but later during infancy the intraluminal antigens, gut microflora and diet, become important determinants in immune programming of human individuals.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here