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Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Transcytosis of IgG01:15

Transcytosis of IgG

Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...

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Updated: Jun 30, 2026

Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
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[Lymphocyte subsets and preeclampsia].

Luz Ma Adriana Balderas Peña1, Carlos Vidal Vizcaíno Magaña, Salvador Hernández Higareda

  • 1Centro Médico Nacional de Occidente, UMAE, Hospital de Especialidades, Unidad de Investigación Médica en Epidemiología Clínica, Guadalajara, Jalisco, México. luz.balderas@cucs.udg.mx

Ginecologia Y Obstetricia De Mexico
|September 20, 2008
PubMed
Summary
This summary is machine-generated.

Preeclampsia may involve immune system dysfunction. Lower levels of CD3+ CD56+ and CD4+ CD25+ lymphocytes were observed in preeclamptic women, suggesting their role in the condition.

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07:51

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Published on: May 21, 2015

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08:19

Isolation of Leukocytes from the Human Maternal-fetal Interface

Published on: May 21, 2015

Area of Science:

  • Immunology
  • Obstetrics

Background:

  • The exact cause of preeclampsia remains unclear, with immune system dysregulation proposed as a contributing factor.
  • This study investigates specific lymphocyte subsets and potential mechanisms behind immune tolerance loss in preeclampsia.

Purpose of the Study:

  • To compare cellular populations of CD3+ CD56+, CD4+ CD25+, T lymphocytes (CD4+ and CD8+), and NK cells between preeclamptic and healthy pregnant women.

Main Methods:

  • Peripheral blood mononuclear cells were analyzed using flow cytometry.
  • Specific lymphocyte subsets, including CD3+ CD56+, CD4+ CD25+, CD4+ T cells, CD8+ T cells, and NK cells, were identified.
  • Statistical analyses included Student's t-test and Pearson correlation to assess differences and relationships.

Main Results:

  • Preeclamptic patients showed a significantly lower percentage of CD3+ CD56+ cells (2.7% vs. 6.1%).
  • A trend towards lower CD4+ CD25+ cell percentages was observed in preeclamptic women (22.11% vs. 33.86%).
  • Mean blood pressure negatively correlated with CD3+ CD56+ cell percentage and CD25 expression on CD4+ T cells.

Conclusions:

  • The findings suggest that CD3+ CD56+ and CD4+ CD25+ lymphocytes play a significant role in the development of preeclampsia.
  • The observed associations support the hypothesis of immune system involvement in preeclampsia pathogenesis.