- Open Access
Submicroscopic infection of placenta by Plasmodium produces Th1/Th2 cytokine imbalance, inflammation and hypoxia in women from north-west Colombia
© Agudelo et al.; licensee BioMed Central Ltd. 2014
- Received: 10 October 2013
- Accepted: 22 March 2014
- Published: 27 March 2014
A large-scale study was set up in order to study the epidemiology, clinical aspects, and immunopathology of gestational and placental malaria in north-west Colombia. In this region, recent reports using a qPCR technique, confirmed frequencies of infection, by Plasmodium falciparum or Plasmodium vivax, up to 45%. Given the high rates of infection observed both in mother and placenta, a first exploratory study was proposed in order to characterize the effect on the inflammation status, tissue damage and hypoxia in Plasmodium spp. infected placentas.
A descriptive, prospective, cross-sectional design was applied to pregnant women with (PM+) and without (PM-) placental malaria. Messenger RNA expression of Fas, FasL; COX-1, COX-2, HIF, VEGF, and the cytokines IL-2, IL-4, IL-10, IFN-γ and TNF, were measured in peripheral and placental blood using a quantitative PCR. The percentage of apoptotic cells was determined with a TUNEL assay.
In total 50 placentas were studied: 25 were positive for submicroscopic infection and 25 were negative for Plasmodium infection. Expression of IL-4 and IL-10 was observed high in placental tissue of PM+, while IL-2 was high in peripheral blood of the same group. Expression of TNF and IFNγ in peripheral blood of the PM + group was high. Similarly, the apoptotic index and Fas expression were significantly high in PM+. However, FasL expression was observed low in PM + compared to PM-. Inflammation markers (HIF, VEGF) and hypoxia markers (COX-1, COX-2) were high in the PM + group.
During placental malaria expression of some pro-inflammatory cytokines is up-regulated and markers of hypoxia and tissue damage are increased in cases of submicroscopic infection.
- Placental malaria
Globally, an estimated 125 million pregnancies are at risk of malaria each year  and the disease causes substantial maternal and infant morbidity/mortality . Both Plasmodium falciparum and Plasmodium vivax can cause adverse pregnancy outcomes, including maternal anaemia and low birth weight, albeit different mechanisms appear to be involved depending on the infecting species . In the case of P. falciparum, adherence of infected erythrocytes to chondroitin sulfate A (CSA), present on the trophoblast surface, is crucial in the pathophysiology of the disease , since parasite sequestration results in inflammatory responses that can be harmful to both the mother and the foetus .
Women inhabiting areas with different degrees of endemicity experience variable exposure to infection and this affects the course of disease . In areas of high stable transmission, as in most sub-Saharan regions, women have significant clinical immunity before pregnancy, and placental malaria is often asymptomatic, but associated with severe maternal anaemia and foetal growth retardation. In these regions, placental malaria is most frequent and severe in first time mothers, and women develop specific immunity against placental forms of infected erythrocytes over successive pregnancies. On the other hand, in areas of low unstable transmission, malaria is symptomatic in women of all parities and is associated with high rates of foetal loss and maternal death . In such regions, increased susceptibility of primigravidae, compared to multigravidae, has been rarely documented .
Recent extensive reviews have focused on the pathogenesis and immunity of gestational and placental malaria caused by P. falciparum, specifically the molecular aspects of these infections, the associated damage to the placenta, and the consequences on the mother, the placenta and the foetus . A significant role for increased cytokines (TNF, IFN-γ and IL-10) and apoptosis in trophoblast damage, low birth weight and preterm delivery during placental malaria, has been observed . Some studies concluded that complications during pregnancy and foetal death observed in P. falciparum placental malaria might be determined by changes in the regulation of apoptosis, via Fas /FasL , and increased Th1 immune responses in the syncytiotrophoblast [10, 11]. In addition, few reports identified a relationship between hypoxia and placental malaria [12, 13], although an association between hypoxia and intrauterine growth retardation was observed in preeclampsia . As for P. vivax infection during pregnancy, these phenomena remain to be studied.
On a routine basis, detection of parasites in placenta requires examination of histological sections of fixed placental tissue or microscopy of placental blood . However, application of highly sensitive molecular techniques confirmed that the frequency of low level (submicroscopic) infections is higher than expected in all endemic regions [16, 17]. Sensitive molecular methods typically diagnose approximately twice as many infections as microscopy. Different authors have suggested that even such low parasitaemia infections can result in pregnancy complications such as maternal anaemia and low birth weight . However, the epidemiological characteristics and the consequences associated with submicroscopic plasmodial infection in pregnant women have been poorly evaluated [19, 20].
Most knowledge gathered about pregnancy-associated malaria resulted from studies in areas of Africa where P. falciparum is highly endemic. In Colombia, where P. vivax represents 60-70% of the total reported cases, malaria in pregnancy constitutes a public health problem [15, 21] with a high frequency of submicroscopic infections [16, 15]. During the past 5 years, several reports contributed to the definition and understanding of the problem of gestational malaria in north-west Colombia [15, 16, 22]. To further recognize the effect of malaria infection on the pathophysiology of placental damage and to define the significance of low level infections in this context, a study was conducted to explore apoptosis, inflammation, and hypoxia in placental tissue, and to measure cytokines in maternal and placental blood, in relation to the presence of submicroscopic placental infection.
Women were recruited from January 2007 to April 2011, at the hospital obstetric facilities in the municipalities of Monteria (08°45′N, 75°53′W), and Puerto Libertador (07°53′35′ N, 75°40″16″ W) of the Uraba-Sinu-San Jorge-Bajo Cauca region of Colombia. This region has an estimated area of 43,506 km2, a population of 2.5 million at risk of malaria, with a mean annual parasite index of 35.8 cases/1,000 inhabitants . The region has a low and stable malaria transmission intensity, with no marked fluctuations in the number of malaria cases during the year. The recorded prevalence of gestational malaria in the region was 9.1% by thick smear and 14.0% by PCR, while placental malaria was observed in 3.3% and 16.5%, respectively .
Study design and sample selection
The study was part of a larger project aimed at exploring the epidemiology, clinical aspects and immunopathology of gestational and placental malaria in north-west Colombia, from which partial results have been reported elsewhere [21, 24]. A total 2,000 pregnant women were recruited in a sequential fashion for the main study. Clinical and epidemiological surveys were applied to all those women. Based on the availability and quality of material collected from peripheral blood and placental tissue, a subset of subjects was selected from the records of the 2,000 women recruited in the main project, to explore the effect of malaria infection on the pathophysiology of placental damage. Regardless of the time of the year or the year of collection, a total 50 subjects, non-matched, were studied: 25 with confirmed placental infection and 25 without Plasmodium spp. infection. The status of infection was defined by thick smear and real-time PCR (qPCR) of placental blood. Positive infected units were those with a negative diagnosis by microscopy and a positive qPCR result; negative units were negative by both tests.
Inclusion and exclusion criteria
Inclusion criteria were voluntary acceptance to participate in the study, signature of the informed consent, permanent residency (>1 year) in the malaria endemic region, negative history of pre-eclampsia and negative HIV and TORCH tests. The exclusion criterion was withdrawal of consent.
Data and specimen collection
After enrolment, a questionnaire was completed which recorded data including age, number of pregnancies, number of malaria episodes during the ongoing pregnancy (based on antenatal records) and antimalarial treatment administered. In addition, labour/delivery and infant outcomes data, as well as maternal haemoglobin value, were obtained from the delivery chart. Placentas were processed immediately after delivery and maternal peripheral blood was obtained within 24 hours. After cleaning with saline, two ~1 cm3 sections of placenta were removed from the maternal side of the organ and blood was collected by aspiration into a tube containing EDTA. From mothers, 3 ml of peripheral blood was obtained and collected into EDTA containing vials. Thick smears were prepared from placental and mother’s blood and blood spots (approximately 100 μl of blood) were placed onto Whatman 3 mm filter paper for molecular diagnosis. One tissue fragment was preserved in RNA later® before processing for expression of markers of apoptosis, hypoxia and inflammation, and the remaining tissue fragment was fixed with 10% buffered formalin (pH 7.0-7.4), before embedding in paraffin, for the TUNEL assay.
Diagnosis of infection by Plasmodium
Plasmodium infection was evaluated in mother’s peripheral and placental blood by microscopy of Field-stained thick films and qPCR. An experienced microscopist based at the field laboratory determined the presence of infection by counting the number of parasites per 200 leukocytes, based on a mean count of 8,000 leukocytes per microliter of blood. Samples were negative when no parasites were detected in 200 high power (100x) fields. For the qPCR, DNA was extracted from a 6 mm2 fragment of placenta using the Chelex method described by Plowe et al.. A qPCR was performed as described previously . Briefly, samples were first tested for Plasmodium using a genus-specific set of primers and probe. The reaction was performed in a final volume of 25 μl containing 5 μl of DNA, 12.5 μl of TaqMan universal master mix (Applied Biosystems), 200 nM of each primer (Plasmo1 and Plasmo2), 50 nM of Plasprobe on the ABI 7500 FAST platform, under universal cycling conditions as published. Samples with a cycle threshold (Ct) value under 45 were tested in a duplex species-specific real-time PCR reaction for P. falciparum and P. vivax.
Expression analysis of cytokines and markers of tissue damage and inflammation
Primers and probes used in this study
Marker and cytokine gene
Product Size (pb)
Quantification of apoptosis
Apoptosis in placentas was assessed by a TUNEL assay as described earlier . Placental sections were deparaffinized and placed on Fisherbrand Superfrost Plus® slides. Detection of cells undergoing apoptosis was performed using the kit DeadEnd Colorimetric System® Promega TUNEL, according to the manufacturer’s protocol. The apoptotic index was calculated based on the proportion of TUNEL stained cells observed in 10 fields (40x). The test was performed in a blinded fashion, for this samples were assigned a code which was revealed once all results were available.
Data were analysed using Excel and SPSS 19. Significance was set at p < 0.05. Non-parametric tests were used for data analysis and the U Mann–Whitney test and the Kruskal-Wallis test were used for correlations. According to the data distribution, the variable number of DNA copies/μl of template was grouped by convenience as follows: Group 1 (0 copies-no infection); Group 2 (0.01 to 1.99 copies/μl), Group 3 (2.00 to 100 copies/μl), and Group 4 (> 100 copies/μl) .
Pregnant women or guardians (in case of <18 years of age) signed a voluntary consent form. The study involved a minor risk and approval was granted by the Comite de Etica of Instituto de Investigaciones Medicas, Facultad de Medicina, Universidad de Antioquia (Approval Certificate number IIM 889ADV).
General characteristics of parturient women participating in the study, according to placental infection status by qPCR
Placental malaria by qPCR
No (N = 25)
Yes (N = 25)
Age of mother (years)
22.43 (range 14–36)
Number of gestations
1.84 (range 0–6)
1.91 (range 0–6)
Weeks of pregnancy
37.6 (range 32–41)
38.3 (range 27–41)
Mother’s haemoglobin (g/dL) at delivery
11.38 (range 7.15–18.30)
10.83 (range 9.00–13.30)
Identification of infecting species in mother’s peripheral blood
19* (11 P. falciparum, 7 P. vivax, 1 mixed)
Birth weight (grams)
2,891 (range 1,780–3,900)
3,305 (range 2,600–4,400)
Cytokine expression in pregnant women and placentas
Cytokine expression (Mean ratio ± standard deviation) in placental tissue and maternal peripheral blood according to the infection status
P (U Mann–Whitney)
1.00 ± 0.42
0.96 ± 0.30
9.00 ± 0.811
0.46 ± 0.37
6.16 ± 0.75
0.83 ± 0.45
1.60 ± 0.40
1.05 ± 0.62
3.50 ± 0.93
0.18 ± 0.18
Maternal peripheral blood
3.65 ± 1.11
1.18 ± 0.50
6.53 ± 2.38
1.10 ± 0.72
1.53 ± 0.41
0.76 ± 0.46
1.63 ± 0.34
1.41 ± 0.50
2.45 ± 0.64
0.65 ± 0.50
Cytokine mean (standard deviation) expression ratio in placenta and maternal peripheral blood according to plasmodial species
Maternal peripheral blood
PM + Pf
PM + Pv
PM + mixed
PM + Pf
PM + Pv
PM + mixed
PM + Pf
PM + Pv
PM + mixed
PM + Pf
PM + Pv
PM + mixed
PM + Pf
PM + Pv
PM + mixed
Apoptosis, inflammation and hypoxia markers in placental malaria
Ratio of expression and proportion of apoptotic cells in placental tissue in infected and uninfected placentas
Infected (n = 25)
Uninfected (n = 25)
P (U Mann–Whitney)
62.37% ± 10.02%
44.88% ± 2.15
6.53 ± 2.49
3.42 ± 0.84
5.60 ± 2.13
6.95 ± 1,16
0.96 ± 1.15
0.21 ± 0.22
0,14 ± 0.14
0.12 ± 0.15
6.95 ± 3.14
0.73 ± 0.41
2.86 ± 0.99
0.42 ± 0.29
The inflammation markers HIF and VEGF were observed high in the PM + group, but only VEGF was significantly different. As for the hypoxia markers, COX-1 and COX-2, both were significantly high in the PM + group. In general, all evaluated markers of tissue damage were up regulated in the placentas of the PM + group (Table 5).
Mean value (standard deviation) of Apoptosis index and ratio (standard deviation) of expression of inflammation and hypoxia markers according to plasmodial species infecting the placenta
PM + Pfa
PM + Pva
PM + mixed
Apoptotic cells index
Relationship between markers of apoptosis/inflammation/hypoxia and cytokine expression in placenta
Correlation (rho, p) between the expression of cytokines and the expression of markers of apoptosis, hypoxia and inflammation in placental tissue, regardless of the infection status (n = 50)
Apoptotic cells (%)
Relatioship between biomarkers of apoptosis/inflammation/hypoxia and placental parasite density in placenta
Placental parasite density was calculated using a qPCR assay as detailed in the methods section. In order to facilitate analysis, and based on the frequency distribution of data, results were categorized according to the copies of parasite DNA measured per PCR μl of total purified DNA: Group 1 (0 copies-no infection); Group 2 (0.01 to 1.99 copies/μl), Group 3 (2.00 to 100 copies/μl), and Group 4 (> 100 copies/μl) . In general, significant differences were observed between Group 1 and the remaining groups as a whole. Copy number correlated positively and significantly with the percentage of apoptotic cells, and expression of Fas, COX1, COX2, HIF, IFN-γ, TNF, IL-4 and IL-10 (p = 0.000 and for IL4 p = 0.017). However, no significant correlation (p ≥ 0.078) was observed between expression of FasL, VEGF and IL-2 in relation to the copies of parasite DNA.
Although the effects of malaria infection on the mother and the foetus depend upon multiple factors, the host immune response and the histopathology of the placenta are specifically associated with complications observed before birth and around the neonatal period . This study evaluated the important immunological aspects and molecular mechanisms associated with tissue damage in the placenta, which contribute to the understanding of the pathophysiology of placental infection. Complex cellular and molecular mechanisms, such as apoptosis, hypoxia and inflammation have not been evaluated in cases of placental infection by Plasmodium spp in this endemic region. Such mechanisms are important to a healthy pregnancy since they contribute to implantation and promote placental development .
This is a first exploratory study on the subject in women from a region where both P. falciparum and P. vivax are endemic and is the first study to report on apoptosis and tissue injury during submicroscopic placental infection. All studied groups came from the same malaria endemic region as to control for any socio-epidemiology associated bias. According to a recent report , most placental infections at delivery in this region were sub-clinical and thick smear microscopy examination failed to diagnose them. Based on these findings, the current study included subjects in which diagnosis of infection was confirmed by qPCR.
Changes in apoptosis have been scarcely studied in placental malaria. In other pathologies such as preeclampsia, the high rate of apoptosis has been directly linked with intrauterine growth restriction . Importantly, the apoptotic index in the PM + placentas herein studied was higher than in PM-. Early reports on apoptosis in malaria infected placentas showed no difference in the proportion of apoptotic cells when compared to uninfected ones . A possible explanation for the dissimilar results from those reported here might be the application of different techniques- TUNEL vs. haematoxylin-eosin staining.
Fas and FasL expression have been proposed as markers of apoptosis, and this is considered an important mechanism by which cytokines act locally and may influence critical signaling processes. In in vitro studies with cell models and placental tissue explants stimulated with pro-inflammatory cytokines, the expression of Fas and FasL was high and similar to the results reported here . Taken together, these observations implicate apoptosis as a host response or a downstream effect of malaria infection in the placenta.
In the current study, increased apoptosis in infected placentas was also associated with high expression of the pro-inflammatory cytokines IFN-γ and TNF. Similar observations with increased expression of Th1 cytokines such as IL-2, TNF, IFN-γ and decreased Th2 cytokines such as IL-6 and TGF-β have been reported by others , and haemozoin deposition and haemozoin-loaded macrophages have implicated in the induction of inflammation in the throphoblast [30, 32]. Ongoing studies are exploring the association between haemozoin deposits and the cytokine profile in infected placentas in Colombia.
Other authors, based on high levels detected in serum of women with gestational malaria, have proposed IL-10 as biomarker of placental infection  and a definitive marker of inflammation during placental malaria . This hypothesis is supported in the current study by the higher expression of IL-10 observed in the infected vs. uninfected placentas. The increased expression of this cytokine in cases of submicroscopic infection is a novel and promising finding.
Hypoxia has been associated with complications from placental malaria infection . However, few studies have explored the relationship between malaria and placental hypoxia . Common histological changes associated with infection such as basal membrane thickening, mononuclear infiltrates and presence of parasites in the intervillous space, affect oxygen transport across the placenta. Some hypoxia mechanisms include oxygen consumption by infiltrating cells, decreased blood perfusion and reduction of the effective foetal-maternal surface area . In consequence, a physiological adaptation to hypoxia results in syncytial knot formation, an alteration often reported during placental infection by Plasmodium. Similar to the current report, Boeuf and colleagues in 2008, observed increased expression of HIF-1α and VEGF during placental infection, however not direct association between placental malaria and hypoxia could be confirmed .
Cyclooxygenase (COX) and lipoxygenase (LOX) transform fatty acids into prostaglandins and leukotrienes, which play important roles in pregnancy and foetal development. In addition, COX-2 has been proposed as a marker of preeclampsia and recovery after infectious conditions . In a study published by Sarr et al., increased expression of COX-2 and IL-10 in chronic placental malaria was detected, and COX-2 was associated with maternal anaemia, placental macrophage infiltration and haemozoin deposition . These results are consistent with the findings herein reported regarding increased COX-2 and IL-10 in cases of placental infection. Furthermore, COX-1 is reported for the first time in association with placental malaria.
Interestingly, no differences were observed between the changes in the markers studied in P. vivax infected placentas compared with those infected with P. falciparum. Some complications of P. vivax infection might be explained by the production of pro-inflammatory cytokines, which alter the balance at the foetal-maternal interface. Based on this, it is hypothesized that P. vivax is as pathogenic as P. falciparum, regardless of the presence of sequestering parasites.
The knowledge gathered so far on the pathophysiology of placental malaria mainly describes cases of P. falciparum infection. The current results demonstrate that P. vivax might also be equivalent in the pathophysiology of placental damage. These results need to be complemented with a study of a large series of P. vivax infected placentas. In addition, the role of naturally acquired specific humoral immunity should complement these studies in order to clarify its implication on clinical status. Finally, studies of the consequences of P. vivax placental infection in Asia and America in the context of a pregnancy vaccine and intermittent preventive therapy should be a priority.
In conclusion, submicroscopic placental infection by malaria parasites failed to induce major clinical effects on mother or foetus but associated with a pro-inflammatory cytokine profile, regardless of the infecting species, and this was more evident in the placental tissue. Finally, increased apoptosis was common in Plasmodium spp. infected placentas.
The authors are grateful to the participating patients, field assistants, employees and managers of the local hospitals for their collaboration, Ms. Sandra Shokoples and Dr. Sédami Gnidehou for assistance in the laboratory.
This work was supported by the Colciencias (project codes 111549326134 and 111556933361); the Universidad de Antioquia (project code IIM 8764–2557); Estrategia de Sostenibilidad 2013–2014, and Banco de la Republica (code 3069).
- Dellicour S, Tatem AJ, Guerra CA, Snow RW, ter Kuile FO: Quantifying the number of pregnancies at risk of malaria in 2007: a demographic study. PLoS Med. 2010, 7: e1000221-10.1371/journal.pmed.1000221.PubMed CentralView ArticlePubMedGoogle Scholar
- Desai M, ter Kuile FO, Nosten F: Epidemiology and burden of malaria in pregnancy. Lancet Infect Dis. 2007, 7: 93-104. 10.1016/S1473-3099(07)70021-X.View ArticlePubMedGoogle Scholar
- Rogerson SJ, Hviid L, Duffy PE, Leke RF, Taylor DW: Malaria in pregnancy: pathogenesis and immunity. Lancet Infect Dis. 2007, 7: 105-117. 10.1016/S1473-3099(07)70022-1.View ArticlePubMedGoogle Scholar
- Fried M, Duffy PE: Adherence of Plasmodium falciparum to chondroitin sulfate A in the human placenta. Science. 1996, 272: 1502-1504. 10.1126/science.272.5267.1502.View ArticlePubMedGoogle Scholar
- Umbers AJ, Boeuf P, Clapham C, Stanisic DI, Baiwog F, Mueller I, Siba P, King CL, Beeson JG, Glazier J, Rogerson SJ: Placental malaria-associated inflammation disturbs the insulin-like growth factor axis of fetal growth regulation. J Infect Dis. 2011, 203: 561-569. 10.1093/infdis/jiq080.PubMed CentralView ArticlePubMedGoogle Scholar
- Muehlenbachs A, Fried M, McGready R: A novel histological grading scheme for placental malaria applied in areas of high and low malaria transmission. J Infect Dis. 2010, 202: 1608-1616. 10.1086/656723.PubMed CentralView ArticlePubMedGoogle Scholar
- Nosten F, Rogerson SJ, Beeson JG, McGready R, Mutabingwa TK, Brabin B: Malaria in pregnancy and the endemicity spectrum: what can we learn?. Trends Parasitol. 2004, 20: 425-432. 10.1016/j.pt.2004.06.007.View ArticlePubMedGoogle Scholar
- Uneke CJ: Diagnosis of Plasmodium falciparum malaria in pregnancy in sub-Saharan Africa: the challenges and public health implications. Parasitol Res. 2008, 102: 333-342. 10.1007/s00436-007-0782-6.View ArticlePubMedGoogle Scholar
- Uckan D, Steele A, Cherry , Wang BY, Chamizo W, Koutsonikolis A, Gilbert-Barness E, Good RA: Trophoblasts express Fas ligand: a proposed mechanism for immune privilege in placenta and maternal invasion. Mol Hum Reprod. 1997, 3: 655-662. 10.1093/molehr/3.8.655.View ArticlePubMedGoogle Scholar
- Conroy A, Serghides L, Finney C, Owino SO, Kumar S, Gowda DC, Liles WC, Moore JM, Kain KC: C5a Enhances dysregulated inflammatory and angiogenic responses to malaria in vitro: potential implications for placental malaria. PLoS One. 2009, 4: e4953-10.1371/journal.pone.0004953.PubMed CentralView ArticlePubMedGoogle Scholar
- Lucchi NW, Peterson DS, Moore JM: Immunologic activation of human syncytiotrophoblast by Plasmodium falciparum. Malar J. 2008, 7: 42-10.1186/1475-2875-7-42.PubMed CentralView ArticlePubMedGoogle Scholar
- Boeuf P, Tan A, Romagosa C, Radford J, Mwapasa V, Molyneux ME, Meshnick SR, Hunt NH, Rogerson SJ: Placental hypoxia during placental malaria. J Infect Dis. 2008, 197: 757-765. 10.1086/526521.PubMed CentralView ArticlePubMedGoogle Scholar
- Sarr D, Aldebert D, Marrama L, Frealle E, Gaye A, Brahim HO, Niang M, Dangou JM, Mercereau-Puijalon O, Lehesran J, Jambou R: Chronic infection during placental malaria is associated with up-regulation of cycloxygenase-2. Malar J. 2010, 9: 45-10.1186/1475-2875-9-45.PubMed CentralView ArticlePubMedGoogle Scholar
- Gamain B, Smith JD, Viebig NK, Gysin J, Scherf A: Pregnancy-associated malaria: parasite binding, natural immunity and vaccine development. Int J Parasitol. 2007, 37: 273-283. 10.1016/j.ijpara.2006.11.011.View ArticlePubMedGoogle Scholar
- Campos IM, Uribe ML, Cuesta C, Franco-Gallego A, Carmona-Fonseca J, Maestre A: Diagnosis of gestational, congenital, and placental malaria in Colombia: comparison of the efficacy of microscopy, nested polymerase chain reaction, and histopathology. Am J Trop Med Hyg. 2011, 84: 929-935. 10.4269/ajtmh.2011.10-0507.PubMed CentralView ArticlePubMedGoogle Scholar
- Arango EM, Samuel R, Agudelo OM, Carmona-Fonseca J, Maestre A, Yanow SK: Molecular detection of malaria at delivery reveals a high frequency of submicroscopic infections and associated placental damage in pregnant women from Northwest Colombia. Am J Trop Med Hyg. 2013, 89: 178-183. 10.4269/ajtmh.12-0669.PubMed CentralView ArticlePubMedGoogle Scholar
- McGready R, Tan SO, Ashley EA, Pimanpanarak M, Viladpai-Nguen J, Phaiphun L, Wüstefeld K, Barends M, Laochan N, Keereecharoen L, Lindegardh N, Singhasivanon P, White NJ, Nosten F: A randomised controlled trial of artemether-lumefantrine versus artesunate for uncomplicated Plasmodium falciparum treatment in pregnancy. PLoS Med. 2008, 5: e263-View ArticleGoogle Scholar
- Schantz-Dunn J, Nour NM: Malaria and pregnancy: a global health perspective. Rev Obstet Gynecol. 2009, 2: 186-192.PubMed CentralPubMedGoogle Scholar
- Arango E, Maestre A, Carmona J: Efecto de la infección submicroscópica o policlonal de Plasmodium falciparum sobre la madre y el producto de la gestación Revisión sistemática. Rev Bras Epidemiol. 2010, 13: 373-386. 10.1590/S1415-790X2010000300002.View ArticlePubMedGoogle Scholar
- Rantala AM, Taylor SM, Trottman PA, Luntamo M, Mbewe B, Maleta K, Kulmala T, Ashorn P, Meshnick SR: Comparison of real-time PCR and microscopy for malaria parasite detection in Malawian pregnant women. Malar J. 2010, 9: 269-10.1186/1475-2875-9-269.PubMed CentralView ArticlePubMedGoogle Scholar
- Carmona-Fonseca J, Maestre A: Incidencia de la malaria gestacional, congénita y placentaria en Urabá (Antioquia, Colombia), 2005–2007. Rev Colomb Obstet Ginecol. 2009, 60: 15-Google Scholar
- Carmona-Fonseca J, Arango E, Maestre A: Placental malaria in Colombia: histopathologic findings in Plasmodium vivax and P. falciparum infections. Am J Trop Med Hyg. 2013, 88: 1093-1101. 10.4269/ajtmh.12-0363.PubMed CentralView ArticlePubMedGoogle Scholar
- Padilla JC, Uribe G, Araújo RM, Narváez PC, Valencia SH: Epidemiology and control of malaria in Colombia. Mem Inst Oswaldo Cruz. 2011, 106: 114-122.View ArticleGoogle Scholar
- Agudelo OM, Arango EM, Maestre A, Carmona-Fonseca J: Prevalence of gestational, placental and congenital malaria in north-west Colombia. Malar J. 2013, 12: 341-10.1186/1475-2875-12-341.PubMed CentralView ArticlePubMedGoogle Scholar
- Plowe CV, Djimde A, Bouare M, Doumbo O, Wellems TE: Pyrimethamine and proguanil resistance-conferring mutations in Plasmodium falciparum dihydrofolate reductase: polymerase chain reaction methods for surveillance in Africa. Am J Trop Med Hyg. 1995, 52: 565-568.PubMedGoogle Scholar
- Shokoples SE, Ndao M, Kowalewska-Grochowska K, Yanow SK: Multiplexed real-time PCR assay for discrimination of Plasmodium species with improved sensitivity for mixed infections. J Clin Microbiol. 2009, 47: 975-980. 10.1128/JCM.01858-08.PubMed CentralView ArticlePubMedGoogle Scholar
- Pfaffl MW: A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29: e45-10.1093/nar/29.9.e45.PubMed CentralView ArticlePubMedGoogle Scholar
- Gavrieli Y, Sherman Y, Ben-Sasson SA: Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol. 1992, 119: 493-501. 10.1083/jcb.119.3.493.View ArticlePubMedGoogle Scholar
- Guller S, Ma YY, Fu HH, Krikun G, Abrahams VM, Mor G: The placental syncytium and the pathophysiology of preeclampsia and intrauterine growth restriction: a novel assay to assess syncytial protein expression. Ann N Y Acad Sci. 2008, 1127: 129-133. 10.1196/annals.1434.015.PubMed CentralView ArticlePubMedGoogle Scholar
- Crocker IP, Tanner OM, Myers JE, Bulmer JN, Walraven G, Baker PN: Syncytiotrophoblast degradation and the pathophysiology of the malaria-infected placenta. Placenta. 2004, 25: 273-282. 10.1016/j.placenta.2003.09.010.View ArticlePubMedGoogle Scholar
- Aschkenazi S, Straszewski S, Verwer KM, Foellmer H, Rutherford T, Mor G: Differential regulation and function of the Fas/Fas ligand system in human trophoblast cells. Biol Reprod. 2002, 66: 1853-1861. 10.1095/biolreprod66.6.1853.View ArticlePubMedGoogle Scholar
- Tkachuk AN, Moormann AM, Poore JA, Rochford RA, Chensue SW, Mwapasa V, Meshnick SR: Malaria enhances expression of CC chemokine receptor 5 on placental macrophages. J Infect Dis. 2001, 183: 967-972. 10.1086/319248.View ArticlePubMedGoogle Scholar
- Kossodo S, Monso C, Juillard P, Velu T, Goldman M, Grau GE: Interleukin-10 modulates susceptibility in experimental cerebral malaria. Immunology. 1997, 91: 536-540. 10.1046/j.1365-2567.1997.00290.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Kabyemela ER, Muehlenbachs A, Fried M, Kurtis JD, Mutabingwa TK, Duffy PE: Maternal peripheral blood level of IL-10 as a marker for inflammatory placental malaria. Malar J. 2008, 7: 26-10.1186/1475-2875-7-26.PubMed CentralView ArticlePubMedGoogle Scholar
- Cooke BM, Mohandas N, Cowman AF, Coppel RL: Cellular adhesive phenomena in apicomplexan parasites of red blood cells. Vet Parasitol. 2005, 132: 273-295. 10.1016/j.vetpar.2005.07.002.View ArticlePubMedGoogle Scholar
- Takem EN, D’Alessandro U: Malaria in pregnancy. Mediterr J Hematol Infect Dis. 2013, 5: e2013010-PubMed CentralView ArticlePubMedGoogle Scholar
- Koga K, Aldo PB, Mor G: Toll-like receptors and pregnancy: trophoblast as modulators of the immune response. J Obstet Gynaecol Res. 2009, 35: 191-202. 10.1111/j.1447-0756.2008.00963.x.View ArticlePubMedGoogle Scholar
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