Placental Transfer and Maternally Acquired Neonatal IgG Immunity in Human Immunodeficiency Virus Infection

Transplacental transfer of specific IgG antibodies was studied in 46 pairs of human immunodeficiency virus type 1 (HIV-I)-seropositive women and their neonates and in 53 pairs of healthy HIV-seronegative mothers and their newborns. Neonatal and maternal sera were assessed by nephelometry for total l...

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Published inThe Journal of infectious diseases Vol. 173; no. 5; pp. 1077 - 1084
Main Authors Isabel de Moraes-Pinto, M., Almeida, Ana C. M., Kenj, Grecy, Filgueiras, Thomaz E., Tobias, Wanda, Santos, Amélia M. N., Carneiro-Sampaio, Magda M. S., Farhat, Calil K., Milligan, Paul J. M., Johnson, Peter M., Hart, Charles A.
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.05.1996
University of Chicago Press
Oxford University Press
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Summary:Transplacental transfer of specific IgG antibodies was studied in 46 pairs of human immunodeficiency virus type 1 (HIV-I)-seropositive women and their neonates and in 53 pairs of healthy HIV-seronegative mothers and their newborns. Neonatal and maternal sera were assessed by nephelometry for total levels of serum IgG and by ELISA for IgG antibodies to herpes simplex virus (HSV), varicella-zoster virus (VZV), measles virus, tetanus toxoid, streptolysin O, and Streptococcus pneumoniae capsular antigens. Placental transfer of IgG antibodies to VZV, tetanus toxoid, measles, streptolysin 0, and S. pneumoniae was decreased by maternal HIV infection. Maternal levels of total IgG had an independent effect on transfer of antibodies to HSV, VZV, measles, and S. pneumoniae. Neonatal antibody levels to tetanus toxoid, measles, and S. pneumoniae were significantly lower in the HIV group. Both maternal hypergammaglobulinemia and maternal HIV infection may contribute to these low antibody levels at birth and thus lead to early infection in this high-risk population.
Bibliography:istex:EA9D7143BF3C99DB461B63A8D4D273831D60E0DB
Reprints or correspondence: Prof. C. A. Hart, Dept. of Medical Microbiology, University of Liverpool, P.O. Box 147, Liverpool, L69 3BX, United Kingdom.
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ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/173.5.1077