1997
DOI: 10.1016/s0022-3476(97)80014-5
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Detection of maternofetal transfusion by placental alkaline phosphatase levels

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Cited by 46 publications
(33 citation statements)
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“…Association of PLAP and IgE levels in maternal blood with those in cord blood. We measured, in paired maternal-and cord-blood samples, the levels of PLAP and polyclonal IgE, 2 molecules that are produced at high levels in women but not in the fetus [21]. Because these molecules do not cross the intact placenta during gestation [21], they have been previously used as markers of maternofetal transfusion during the peripartum period [7,21,24,25].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Association of PLAP and IgE levels in maternal blood with those in cord blood. We measured, in paired maternal-and cord-blood samples, the levels of PLAP and polyclonal IgE, 2 molecules that are produced at high levels in women but not in the fetus [21]. Because these molecules do not cross the intact placenta during gestation [21], they have been previously used as markers of maternofetal transfusion during the peripartum period [7,21,24,25].…”
Section: Resultsmentioning
confidence: 99%
“…The PLAP level was measured in maternal-and cord-blood samples, by use of the method of Kaneda et al [21] as modified by Kwiek et al [22]. The PLAP level in cord and maternal blood was determined by interpolation from a standard curve of purified hu- man PLAP (Sigma) fit to a quadratic equation.…”
Section: Study Population Healthy Pregnant Women Residing In Kwalementioning
confidence: 99%
“…30,31 More recent studies assessing HBsAg and placental alkaline phosphatase levels in infants suggest that approximately 3 ml of maternal blood is present within the fetal circulation following uncomplicated vaginal delivery. 32,33 The amount of maternal blood within the fetal circulation is substantially lower following elective, scheduled C-section, but is not decreased following C-section in labor. Thus, maternal-tofetal microtransfusion could result in some HIV-infected maternal cells within the fetal circulation potentially leading to allostimulation-induced virus production.…”
Section: Discussionmentioning
confidence: 99%
“…If one accepts the proposed concept that microchimerism potentially predisposes to autoimmune diseases [11,12,20,21], then volume of cell traffic between maternal and fetal compartments may matter in how a potential genetic risk is phenotypically expressed. Maternalefetal traffic is reduced by cesarean section [8], while fetalematernal cell traffic is increased by cesarean section [7,9]. As the Fig.…”
Section: Discussionmentioning
confidence: 99%