Reduced Transplacental Transfer of a Subset of Epstein-Barr Virus-Specific Antibodies to Neonates of Mothers Infected with Plasmodium falciparum Malaria during Pregnancy

Author:

Ogolla Sidney12,Daud Ibrahim I.13,Asito Amolo S.14,Sumba Odada P.1,Ouma Collins2,Vulule John1,Middeldorp Jaap M.5,Dent Arlene E.6,Mehta Saurabh7,Rochford Rosemary8

Affiliation:

1. Center for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya

2. Maseno University, Kisumu, Kenya

3. Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya

4. School of Physical and Biological Sciences, Jaramogi Oginga Odinga University of Science and Technology, Bondo, Kenya

5. Department of Pathology, VU University Medical School, Amsterdam, The Netherlands

6. Case Western Reserve University, Cleveland, Ohio, USA

7. Division of Nutritional Sciences, Cornell University, Ithaca, New York, USA

8. Department of Microbiology and Immunology, State University of New York Upstate Medical University, Syracuse, New York, USA

Abstract

ABSTRACT Over 35% of children in a region of malaria endemicity are infected with Epstein-Barr virus (EBV) by 6 months of age. This susceptibility may be linked to impaired transplacental transfer of antibodies. In this study, we determined the effect of malaria exposure during pregnancy on the transfer of EBV-specific maternal antibodies in a region of western Kenya that experiences endemic malaria. Pregnant mothers were recruited and followed up until delivery to determine levels of neonatal malaria exposure. Levels of EBV lytic (viral capsid antigen [VCA], Z transcriptional activator [Zta], and early diffuse antigen complex [EAd]) and EBV latent (EBV nuclear antigen-1 (EBNA1]) and tetanus-specific IgG antibodies were measured in 70 paired maternal and cord blood samples using a Luminex-bead-based assay. A high proportion (63%) of the infants were exposed to malaria in utero . Levels of EBV- and tetanus-specific antibodies were similar in malaria-infected mothers and in mothers who had no detectable malaria infection. Malaria-exposed neonates had significantly lower levels of anti-EBNA1, anti-Zta, and anti-EAd antibodies than were seen in their mothers. In utero malaria exposure resulted in significant reductions in transplacental transfer of anti-VCA-p18 and anti-EBNA1 antibodies of 13% and 22%, respectively. Neonates received significantly low levels of anti-Zta and anti-EAd antibodies irrespective of malaria exposure levels. In multivariate analysis, in utero malaria exposure was associated with a significant reduction in the transfer of anti-VCA-p18 and anti-EBNA1 antibodies to the neonates ( P = 0.0234 and P = 0.0017, respectively). Malaria during pregnancy results in differential levels of transfer of EBV-specific antibodies from the mother to the fetus. The impaired transplacental transfer of some antibodies may lead to the malaria-exposed neonates being susceptible to early EBV infection.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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