This Article Full Text Full Text (PDF) Other Versions of this Article: IAI.00964-07v1 76/4/1527    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Kabyemela, E. R. Articles by Duffy, P. E. Search for Related Content PubMed PubMed Citation Articles by Kabyemela, E. R. Articles by Duffy, P. E.

 Previous Article  |  Next Article 

Infection and Immunity, April 2008, p. 1527-1534, Vol. 76, No. 4
0019-9567/08/$08.00+0     doi:10.1128/IAI.00964-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Fetal Responses during Placental Malaria Modify the Risk of Low Birth Weight

MOMS Project, Seattle Biomedical Research Institute, Seattle, Washington 98109, and Muheza Designated District Hospital, Muheza, Tanzania,¹ Tumaini University, Moshi, Tanzania,² University of Washington, Seattle, Washington 98195,³ Brown University, Providence, Rhode Island,⁴ National Institute for Medical Research, Dar-Es-Salaam, Tanzania⁵

Received 15 July 2007/ Returned for modification 27 September 2007/ Accepted 15 January 2008

Inflammation during placental malaria (PM) is associated with low birth weight (LBW), especially during the first pregnancy, but the relative contribution of maternal or fetal factors that mediate this effect remains unclear and the role of gamma interferon (IFN-) has been controversial. We examined the relationship of maternal and cord plasma levels of IFN-, tumor necrosis factor alpha, interleukin-10, ferritin, and leptin to birth weight for Tanzanian women delivering in an area where there is a high rate of malaria transmission. The placental levels of inflammatory cytokines, including IFN-, increased significantly during PM in primigravid and multigravid women but not in secundigravid women. PM also increased maternal peripheral levels of all inflammatory markers except IFN- but had strikingly little effect on cord levels of these proteins. In a multivariate analysis, placental IFN- was negatively associated (P = 0.01) and cord ferritin was positively associated (P < 0.0001) with birth weight in infected (PM-positive [PM⁺]) first-time mothers. This relationship was not observed in other mothers, consistent with the epidemiology of PM and disease. Cord leptin had a strong positive relationship with birth weight in offspring of PM-negative women (P = 0.02 to P < 0.0001) but not in offspring of PM⁺ women (all differences were not significant) in the three gravidity groups. The results confirmed that placental IFN- is related to LBW due to PM during first pregnancies and suggest that fetal ferritin plays a protective role. Because fetal cells are a source of placental IFN- and cord ferritin, the fetal response to PM may modify the risk of LBW.

Published ahead of print on 22 January 2008.

Editor: J. F. Urban, Jr.