Author:
Walther Brigitte,Miles David JC,Waight Pauline,Palmero Melba S,Ojuola Olubukola,Touray Ebrima S,Whittle Hilton,van der Sande Marianne,Crozier Sarah,Flanagan Katie L
Abstract
Abstract
Background
Placental malaria (PM) is associated with prenatal malaise, but many PM+ infants are born without symptoms. As malaria has powerful immunomodulatory effects, we tested the hypothesis that PM predicts reduced T-cell responses to vaccine challenge.
Methods
We recruited healthy PM+ and PM- infants at birth. At six and 12 months, we stimulated PBMCs with tuberculin purified protein derivative (PPD) and compared expression of CD154, IL-2 and IFNγ by CD4 T-cells to a negative control using flow cytometry.
We measured the length, weight and head circumference at birth and 12 months.
Results
IL-2 and CD154 expression were low in both groups at both timepoints, without discernable differences. Expression of IFNγ was similarly low at 6 months but by 12 months, the median response was higher in PM- than PM + infants (p = 0.026). The PM+ infants also had a lower weight (p = 0.032) and head circumference (p = 0.041) at 12 months, indicating lower growth rates.
At birth, the size and weight of the PM+ and PM- infants were equivalent. By 12 months, the PM+ infants had a lower weight and head circumference than the PM- infants.
Conclusions
Placental malaria was associated with reduced immune responses 12 months after immune challenge in infants apparently healthy at birth.
Publisher
Springer Science and Business Media LLC
Cited by
20 articles.
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