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Interleukin-4 deficiency induces mild preeclampsia in mice

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miR-125b Enhances IL-8 Production in Early-Onset Severe Preeclampsia by Targeting Sphingosine-1-Phosphate Lyase 1

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Unique maternal immune and functional microbial profiles during prenatal stress

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Cytokine Imprint in Preeclampsia

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Aspirin for Prevention of Preeclampsia in Lupus Pregnancy

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Inflammatory processes are specifically enhanced in endothelial cells by placental-derived TNF-α: Implications in preeclampsia (PE)

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ADAMTS13, FVIII, von Willebrand factor, ABO blood group assessment in preeclampsia

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The influence of oxidative stress and autophagy cross regulation on pregnancy outcome

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Preeclamptic Women Have Decreased Circulating IL-10 (Interleukin-10) Values at the Time of Preeclampsia Diagnosis

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Maternal inflammatory response to microbial invasion of the amniotic cavity: analyses of multiple proteins in the maternal serum

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Increased Serum Levels of Inflammatory Mediators and Low Frequency of Regulatory T Cells in the Peripheral Blood of Preeclamptic Mexican Women

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Choline Supplementation During Pregnancy Protects Against Gestational Lipopolysaccharide-Induced Inflammatory Responses

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Biomarkers of Plasmodium falciparum Infection during Pregnancy in Women Living in Northeastern Tanzania

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Inflammatory Markers in the Second Trimester Prior to Clinical Onset of Preeclampsia, Intrauterine Growth Restriction, and Spontaneous Preterm Birth

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Overlap of proteomics biomarkers between women with pre-eclampsia and PCOS: a systematic review and biomarker database integration

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Regulatory T‐cell Subpopulations in Severe or Early‐onset Preeclampsia

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Fibrinogen, an endogenous ligand of Toll-like receptor 4, activates monocytes in pre-eclamptic patients

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CXCR4, CXCR7, and CXCL12 are associated with trophoblastic cells apoptosis and linked to pathophysiology of severe preeclampsia

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Impact of Preeclampsia on the Relationship between Maternal Asthma and Offspring Asthma. An Observation from the VDAART Clinical Trial

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Ameliorative effects of pre-eclampsia by quercetin supplement to aspirin in a rat model induced by L-NAME

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Polymorphisms and Plasma Level of Transforming Growth Factor-Beta 1 and Risk for Preeclampsia: A Systematic Review

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Possible Association of IL-4 VNTR Polymorphism with Susceptibility to Preeclampsia

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Supplementation of maternal omega-3 fatty acids to pregnancy induced hypertension Wistar rats improves IL10 and VEGF levels

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Serum Inflammatory Markers and Preeclampsia in Type 1 Diabetes

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Decreased Seizure Threshold in an Eclampsia-Like Model Induced in Pregnant Rats with Lipopolysaccharide and Pentylenetetrazol Treatments

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Angiogenic factor screening in women with mild preeclampsia – New and significant proteins in plasma

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Increased expression of IFN‑γ in preeclampsia impairs human trophoblast invasion via a SOCS1/JAK/STAT1 feedback loop

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Changes in Serum Cytokines Throughout Pregnancy in Women With Polycystic Ovary Syndrome

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Accumulation of Advanced Glycation End Products Involved in Inflammation and Contributing to Severe Preeclampsia, in Maternal Blood, Umbilical Blood and Placental Tissues

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The expression of pentraxin 3 and tumor necrosis factor-alpha is increased in preeclamptic placental tissue and maternal serum

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IL-27 Activates Human Trophoblasts to Express IP-10 and IL-6: Implications in the Immunopathophysiology of Preeclampsia

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Residual vascular dysfunction in women with a history of preeclampsia

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Lipid profile and cytokines in hypertension of pregnancy: A comparison of preeclampsia therapies

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Vitamin D restores angiogenic balance and decreases tumor necrosis factor‐α in a rat model of pre‐eclampsia

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IL-10: A bridge between immune cells and metabolism during pregnancy

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Elevated concentration of cytokines in aqueous in post‐vitrectomy eyes

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Analysis of interleukin-18 promoter polymorphisms and changes in interleukin-18 serum levels underscores the involvement of interleukin-18 in recurrent spontaneous miscarriage

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Genetic variations in IL1A and IL1RN are associated with the risk of preeclampsia in Chinese Han population

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Perinatal Micro-Bleeds and Neuroinflammation in E19 Rat Fetuses Exposed to Utero-Placental Ischemia

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Cytokines and pregnancy: Potential regulation by histone deacetylases

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Sex-specific impact of maternal–fetal risk factors on depression and cardiovascular risk 40 years later

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Severe preeclampsia: Are hemostatic and inflammatory parameters associated?

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Calcium-Vitamin D co-supplementation affects metabolic profiles, but not pregnancy outcomes, in healthy pregnant women

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Association of high-sensitivity C-reactive protein serum levels in early pregnancy with the severity of preeclampsia and fetal birth weight

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Decreased circulating anandamide levels in preeclampsia

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The NLRP3 rs10754558 polymorphism is a risk factor for preeclampsia in a Chinese Han population

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High-density lipoproteins (HDL) composition and function in preeclampsia

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Abnormal uterine inflammation in obstetric syndromes: molecular insights into the role of chemokine decoy receptor D6 and inflammasome NLRP3

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Anti-Inflammatory and Antioxidant Activities of Terpene- and Polyphenol-Rich Premna odorata Leaves on Alcohol-Inflamed Female Wistar Albino Rat Liver

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Mesenchymal stromal cell-derived extracellular vesicle therapy prevents preeclamptic physiology through intrauterine immunomodulation†

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Placental ischemia increases seizure susceptibility and cerebrospinal fluid cytokines

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Changes in the structure and function of the brain years after Pre-eclampsia

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Promoter region polymorphisms in the transforming growth factor beta-1 (TGFβ1) gene and serum TGFβ1 concentration in preeclamptic and control Iranian women

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High levels of HtrA4 observed in preeclamptic circulation drastically alter endothelial gene expression and induce inflammation in human umbilical vein endothelial cells

Wang, Y., & Nie, G. (2016) · Placenta · doi:10.1016/j.placenta.2016.09.003 · Cited by 30

Pre-eclampsia: the role of highly active antiretroviral therapy and immune markers

Phoswa, W. N., Naicker, T., Ramsuran, V., & Moodley, J. (2018) · Inflammation Research · doi:10.1007/s00011-018-1190-3 · Cited by 32

Placental inflammation by HMGB1 activation of TLR4 at the syncytium

Tangerås, L. H., Silva, G. B., Stødle, G. S., Gierman, L. M., Skei, B., Collett, K., Beversmark, A. L., Skråstad, R. B., Thomsen, L. C. V., Bjørge, L., et al. (2018) · Placenta · doi:10.1016/j.placenta.2018.10.011 · Cited by 30

Pathophysiological impact of CXC and CX3CL1 chemokines in preeclampsia and gestational diabetes mellitus

Ullah, A., Zhao, J., Singla, R. K., & Shen, B. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1272536 · Cited by 29

Metformin exhibits its therapeutic effect in the treatment of pre-eclampsia via modulating the Met/H19/miR-148a-5p/P28 and Met/H19/miR-216-3p/EBI3 signaling pathways

Shu, C., Yan, D., Chen, C., Mo, Y., Wu, L., Gu, J., Shah, N. K., He, J., & Dong, S. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.105693 · Cited by 29

Inhibition of blood-brain barrier efflux transporters promotes seizure in pregnant rats: Role of circulating factors

Johnson, A. C., Hammer, E., Sakkaki, S., Tremble, S. M., Holmes, G. L., & Cipolla, M. J. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.07.017 · Cited by 28

Relationship between low maternal vitamin D status and the risk of severe preeclampsia: A case control study

Pashapour, S., Golmohammadlou, S., Behroozi-Lak, T., Ghasemnejad-Berenji, H., Sadeghpour, S., & Ghasemnejad‐Berenji, M. (2019) · Pregnancy Hypertension · doi:10.1016/j.preghy.2019.01.003 · Cited by 30

Preeclampsia may influence offspring neuroanatomy and cognitive function: a role for placental growth factor†

Kay, V. R., Rätsep, M. T., Figueiró-Filho, E. A., & Croy, B. A. (2019) · Biology of Reproduction · doi:10.1093/biolre/ioz095 · Cited by 30

Trophoblast‐derived CXCL12 promotes CD56brightCD82−CD29+ NK cell enrichment in the decidua

Lü, H., Jin, L., Huang, H., Ha, S., Yang, H., Chang, R., Li, D., & Li, M. (2019) · American Journal of Reproductive Immunology · doi:10.1111/aji.13203 · Cited by 28

The Role of Ergothioneine in Red Blood Cell Biology: A Review and Perspective

Thomas, T. A., Francis, R. O., Zimring, J. C., Kao, J. P. Y., Nemkov, T. G., & Spitalnik, S. L. (2024) · Antioxidants · doi:10.3390/antiox13060717 · Cited by 27

Analysis of gene expression identifies candidate markers and pathways in pre-eclampsia

He, P., Shao, D., Ye, M., & Zhang, G. (2014) · Journal of Obstetrics and Gynaecology · doi:10.3109/01443615.2014.990430 · Cited by 27

Cytokine-polymorphisms associated with Preeclampsia: A review

Mora-Palazuelos, C. E., Bermúdez, M., Aguilar‐Medina, M., Ramos‐Payán, R., Ayala-Ham, A. D. R., & Romero-Quintana, J. G. (2022) · Medicine · doi:10.1097/md.0000000000030870 · Cited by 27

Increased prevalence of peripheral blood granulysin-producing cytotoxic T lymphocytes in preeclampsia

Molvarec, A., Shiozaki, A., Ito, M., Toldi, G., Stenczer, B., Szarka, A., Nakashima, A., Vásárhelyi, B., Rigó, J. J., & Saito, S. (2011) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2011.03.012 · Cited by 27

Exposure to preeclampsia in utero affects growth from birth to late childhood dependent on child’s sex and severity of exposure: Follow-up of a nested case-control study

Byberg, K. K., Øymar, K. A. A., Eide, G. E., Forman, M. R., & Júlíusson, P. B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176627 · Cited by 27

Progesterone inhibited endoplasmic reticulum stress associated apoptosis induced by interleukin‐1β via the GRP78/PERK/CHOP pathway in BeWo cells

Liu, L., Zhang, Y., Wang, Y., Peng, W., Zhang, N., & Ye, Y. (2017) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.13549 · Cited by 27

Circulating TGF-β1, Glycation, and Oxidation in Children with Diabetes Mellitus Type 1

Jakuš, V., Sapák, M., & Kostolanská, J. (2012) · Experimental Diabetes Research · doi:10.1155/2012/510902 · Cited by 27

Pregnancy-induced Cardiovascular Pathologies: Importance of Structural Components and Lipids

Aleksenko, L., & Quaye, I. K. (2020) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2020.05.014 · Cited by 26

Changes in the maternal cytokine profile in pregnancies complicated by fetal growth restriction

Mullins, E., Prior, T., Roberts, I. A. G., & Kumar, S. (2012) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2012.01132.x · Cited by 26

Circulating levels of IFN-γ, IL-1, IL-17 and IL-22 in pre-eclampsia: A systematic review and meta-analysis

Deng, Z., Zhang, L., Tang, Q., Xu, Y., Liu, S., & Li, H. (2020) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2020.03.039 · Cited by 26

Plasma Lipoproteins and Preeclampsia in Women with Type 1 Diabetes: A Prospective Study

Basu, A., Alaupovic, P., Wu, M., Jenkins, A. J., Yu, Y., Nankervis, A. J., Hanssen, K. F., Scholz, H., Henriksen, T., Lorentzen, B., et al. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-3255 · Cited by 26

Generating Functional Multicellular Organoids from Human Placenta Villi

Huang, L., Tu, Z., Wei, L., Sun, W., Wang, Y., Bi, S., He, F., Du, L., Chen, J., Kzhyshkowska, J. G., et al. (2023) · Advanced Science · doi:10.1002/advs.202301565 · Cited by 25

Dendritic cells derived from preeclampsia patients influence Th1/Th17 cell differentiation in vitro.

Wang, J., Tao, Y., Cheng, X., Zhu, T., Chen, Z., Yao, H., & Su, L. (2014) · PubMed Central · Cited by 25

Low circulating levels of vitamin D may contribute to the occurrence of preeclampsia through deregulation of Treg /Th17 cell ratio

Muyayalo, K. P., Huang, X., Zhu, Q., Li, Z., Mor, G., & Liao, A. (2019) · American Journal of Reproductive Immunology · doi:10.1111/aji.13168 · Cited by 25

Preeclampsia: inflammatory signature of decidual cells in early manifestation of disease

Vishnyakova, P., Poltavets, A. S., Nikitina, M., Muminova, K., Potapova, A., Vtorushina, V. V., Loginova, N. S., Midiber, K. Y., Михалева, Л. М., Lokhonina, А. V., et al. (2021) · Placenta · doi:10.1016/j.placenta.2021.01.011 · Cited by 25

Mitochondrial dysfunction-induced high hCG associated with development of fetal growth restriction and pre-eclampsia with fetal growth restriction

Kiyokoba, R., Uchiumi, T., Yagi, M., Toshima, T., Tsukahara, S., Fujita, Y., Kato, K., & Kang, D. (2022) · Scientific Reports · doi:10.1038/s41598-022-07893-y · Cited by 25

Human Plasma Proteome During Normal Pregnancy

Tarca, A. L., Romero, R. J., Bhatti, G., Gotsch, F., Done, B., Gudicha, D. W., Gallo, D. M., Jung, E., Piqué-Regi, R., Berry, S. M., et al. (2022) · Journal of Proteome Research · doi:10.1021/acs.jproteome.2c00391 · Cited by 27

PP028. Serum cytokine profile in relation to the clinical features and laboratory parameters in women with preeclampsia

Molvarec, A., Szarka, A., Lázár, L., & Rigó, J. (2013) · Pregnancy Hypertension · doi:10.1016/j.preghy.2013.04.055 · Cited by 3

Cytokine mapping of sera from women with preeclampsia and normal pregnancies

Jonsson, Y., Rubèr, M., Matthiesen, L., Berg, G. E., Nieminen, K., Sharma, S., Ernerudh, J., & Ekerfelt, C. (2006) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2005.10.007 · Cited by 256

PL108. Inflammatory mechanisms in preeclampsia

Molvarec, A., & Rigó, J. J. (2015) · Pregnancy Hypertension · doi:10.1016/j.preghy.2015.07.059

Circulating Levels of Immunoreactive Cytokines in Women with Preeclampsia

Conrad, K. P., Miles, T. M., & Benyo, D. F. (1998) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.1998.tb00398.x · Cited by 392

Monocytes of preeclamptic women spontaneously synthesize pro-inflammatory cytokines

Luppi, P., & DeLoia, J. A. (2005) · Clinical Immunology · doi:10.1016/j.clim.2005.11.001 · Cited by 145