Document Detail


Colostral mononuclear phagocytes are able to kill enteropathogenic Escherichia coli opsonized with colostral IgA.
MedLine Citation:
PMID:  9246209     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Enteropathogenic Escherichia coli (EPEC) is the main aetiological agent of acute diarrhoea among low socioeconomic level infants in developing countries. Breast-feeding provides infant protection against acute gastrointestinal and respiratory infections; however, little is known about the protective role of colostral phagocytes in the gut of newborn infants. In the present investigation we studied the ability of human colostral MN phagocytes to kill EPEC as well as the interactions between these cells and colostral and serum opsonins. The authors observed that the microbicidal activity of colostrum MN phagocytes was dependent on previous EPEC opsonization with colostral supernatant or blood serum. A defatted colostrum supernatant pool presented opsonic activity for EPEC killing at levels equivalent to those of normal serum. IgA-depleted colostrum supernatant showed significantly lower opsonic activity, whereas purified IgA from the same colostrum pool was a potent opsonin which induced EPEC killing at levels equivalent to those of untreated colostrum. Colostral MN phagocytes are able to release superoxide anion when incubated with both EPEC opsonized with untreated colostrum and purified IgA. Purified IgA was also able to restore opsonic activity of IgA-depleted colostrum. A colostrum pool without C3 and IgG induced EPEC killing by colostral MN phagocytes at rates equivalent to those of untreated colostrum supernatant. Addition of an IgM MoAb (My43) anti-human Fc alpha receptor resulted in a significant inhibition of EPEC killing when bacteria were opsonized with purified IgA, suggesting an interaction between IgA and Fc alpha R. With respect to serum opsonins, we observed that IgG plus complement component C3 were necessary to induce EPEC killing by the colostrum MN phagocytes. Colostral phagocyte killing of enteropathogenic bacteria may represent an additional mechanism of breast-feeding protein against intestinal infections during the first week of life.
Authors:
A C Honorio-França; M P Carvalho; L Isaac; L R Trabulsi; M M Carneiro-Sampaio
Related Documents :
7136659 - A planned prospective evaluation of the anti-infective property of varying quantities o...
576209 - Metabolic acidosis and infant feeding.
7293949 - Evaluation of lactational performance of navajo women.
558739 - Adequacy of expressed breast milk for early growth of preterm infants.
20930219 - Breast milk expression and maintenance in mothers of very low birth weight infants: sup...
8044629 - Polychlorinated biphenyls in mother milk and adapted cow's milk.
9161309 - Mothers' birth weight and survival of their offspring: population based study.
4078669 - Abolition of feeding intolerance following ophthalmologic examination of neonates.
7136659 - A planned prospective evaluation of the anti-infective property of varying quantities o...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Scandinavian journal of immunology     Volume:  46     ISSN:  0300-9475     ISO Abbreviation:  Scand. J. Immunol.     Publication Date:  1997 Jul 
Date Detail:
Created Date:  1997-08-21     Completed Date:  1997-08-21     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0323767     Medline TA:  Scand J Immunol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  59-66     Citation Subset:  IM    
Affiliation:
Department of Immunology, Universidade de São Paulo, Brazil.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Blood Bactericidal Activity
Colostrum / immunology*
Complement C3 / immunology
Cytotoxicity, Immunologic
Diarrhea / immunology
Escherichia coli / immunology*
Humans
Immunoglobulin A, Secretory / immunology
Immunoglobulin G / immunology
Opsonin Proteins
Phagocytes / immunology*
Receptors, Fc / immunology
Superoxides / metabolism
Chemical
Reg. No./Substance:
0/Complement C3; 0/IgA receptor; 0/Immunoglobulin A, Secretory; 0/Immunoglobulin G; 0/Opsonin Proteins; 0/Receptors, Fc; 11062-77-4/Superoxides

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Efficient in vitro cleavage of mouse acute phase serum amyloid A mRNA mediated by a synthetic hammer...
Next Document:  Immunotherapy affects the seasonal increase in specific IgE and interleukin-4 in serum of patients w...