Advertisement
Research Article Free access | 10.1172/JCI119340
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Malhotra, I. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Ouma, J. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Wamachi, A. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Kioko, J. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Mungai, P. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Omollo, A. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Elson, L. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Koech, D. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by Kazura, J. in: JCI | PubMed | Google Scholar
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106-4983, USA.
Find articles by King, C. in: JCI | PubMed | Google Scholar
Published April 1, 1997 - More info
Neonates exposed to parasite antigens (Ags) in utero may develop altered fetal immunity that could affect subsequent responses to infection. We hypothesized that cord blood lymphocytes (CBL) from offspring of mothers residing in an area highly endemic for schistosomiasis, filariasis, and tuberculosis in Kenya would either fail to respond or generate a predominantly Th2-associated cytokine response to helminth and mycobacterial antigens (PPD) in vitro compared to maternal PBMC. Kenyan CBL generated helminth Ag-specific IL-5 (range 29-194 pg/ml), IL-10 (121-2,115 pg/ml), and/or IFN-gamma (78 pg/ml-10.6 ng/ml) in 26, 46, and 57% of neonates, respectively (n = 40). PPD induced IFN-gamma in 30% of Kenyan CBL (range 79-1,896 pg/ml), but little or no IL-4 or IL-5. No Ag-specific IL-4, IL-5, or IFN-gamma release was detected by CBL obtained in the United States (n = 11). Ag-driven cytokine production was primarily CD4-dependent. Cytokine responses to helminth and mycobacterial Ags by maternal PBMC mirrored that observed in neonates. CBL from helminth infected and/or PPD-sensitized mothers produced more Ag-specific cytokines compared to CBL from uninfected mothers (P < 0.05). These data demonstrate that the human fetus develops similar patterns of cytokine production observed in adults and indicates that prenatal exposure may not lead to tolerance or altered fetal immunity. .