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Ontogeny of cellular immunity in man
Summary
This study reveals the human fetal immune system
Area of Science:
- Immunology
- Developmental Biology
- Fetal Development
Background:
- Understanding the ontogeny of fetal immune responses is crucial for assessing immune competence.
- The sequential development of phytohemagglutinin (PHA) and mixed lymphocyte reaction (MLR) responsiveness in human fetuses remains incompletely defined.
Purpose of the Study:
- To precisely determine the developmental sequence of phytohemagglutinin (PHA) and allogenic cell responsiveness (MLR) acquisition in the human fetus.
- To investigate the timeline of immune cell reactivity in various fetal lymphoid tissues.
Main Methods:
- Quantitative assessment of immune cell reactivity using 3H-thymidine incorporation.
- Analysis of lymphoid tissues from human fetuses at various developmental stages (from 5 weeks fetal age).
Main Results:
- Mixed lymphocyte reaction (MLR) responsiveness was the earliest detectable immune response, first observed in fetal liver lymphoid cells at 5 weeks.
- Phytohemagglutinin (PHA) reactivity emerged later, appearing in thymocytes at 10.5 weeks and in spleen and blood at 14 weeks.
- MLR reactivity was detected in the thymus at 12.5 weeks and in spleen and blood at 14.5 weeks; fetal marrow lymphocytes showed no reactivity up to 18 weeks.
Conclusions:
- The fetal thymus demonstrates immunocompetence by approximately 10.5 weeks of gestation.
- Early MLR responsiveness appears to be regulated by non-thymic (hepatic) factors during fetal development.