Previous Article | Next Article ![]()
Clinical and Diagnostic Laboratory Immunology, Nov 1997, 723-726, Vol 4, No. 6
E Grimprel, E Njamkepo, P Begue and N Guiso
The contribution of maternal pertussis serology comparing prepartum serum
to serum collected during the infant's disease to the diagnosis of
pertussis in infants was evaluated for 28 pairs of young infants with
pertussis syndrome and their mothers and was compared to those of culture
and PCR. Infants had a nasopharyngeal aspiration tested by PCR, and acute
and convalescent sera were collected during their disease. Mothers had a
first acute serum collected concomitantly with the infant's acute serum,
and both acute sera were compared to a prepartum serum. Sera were analyzed
by immunoblotting for the detection of anti- pertussis toxin (PT)
antibodies. Serological evidence of pertussis in infants was assessed as
either an increase in anti-PT antibody levels between the mother's
prepartum and acute sera or the presence of antibodies in the infant's
acute serum and their absence in both the mother's acute and prepartum
sera. Culture and PCR sensitivity were 43 and 89%, respectively. Most
infants (18 of 24) had no pertussis antibody detectable in their acute
sera, confirming a delayed immune response at this age. A comparison of
infant's and mother's serology, using prepartum serum, rapidly confirmed
the diagnosis in 57% of the cases. Although less sensitive than PCR, this
serological method should be used for a rapid diagnosis of pertussis in
young infants when culture and PCR are either not available or negative.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Rapid diagnosis of pertussis in young infants: comparison of culture, PCR, and infant's and mother's serology
Consultation, Urgences, Maladies Infectieuses et Tropicales, Hopital d'Enfants Armand-Trousseau, Paris, France.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»