Evidence to suggest that the human fetal spleen is not a hematopoietic organ
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Updated: Oct 14, 2026

A Mouse Model of Vascularized Heterotopic Spleen Transplantation for Studying Spleen Cell Biology and Transplant Immunity
Published on: June 11, 2019
Abstract:
The human fetal spleen commonly is regarded as an organ of hematopoiesis. Because of the authors' interest in myelofibrosis with myeloid metaplasia (MMM) and because the myeloid metaplasia commonly is regarded as a reactivation of embryonic sites of blood formation, spleens from 48 fetuses and stillborn infants were studied, in an attempt to evaluate splenic hematopoiesis (myelopoiesis). The authors employed immunohistologic and cytochemical technics to identify granulocytic, erythroid, and megakaryocytic cells, in contrast to previous studies that have relied solely on conventional morphology. The authors found surprisingly little evidence of hematopoiesis. Virtually no hematopoietic cells of the dividing cell pool were identified, in spite of the fact that the technic used is capable of detecting such immature forms. The results suggests that the spleen is not a significant organ of hematopoiesis in the human fetus but that immature hematopoietic cells found there merely reflect trapping of circulating precursors in the fetal blood. These findings have significant implications for the pathophysiology of MMM.
Insights
The human fetal spleen is not a significant site of blood formation (hematopoiesis). Immature hematopoietic cells found in the fetal spleen are likely trapped circulating precursors, not actively developing there.
Area of Science:
- Developmental Biology
- Hematology
- Immunology
Background:
- The human fetal spleen is traditionally considered an organ of hematopoiesis.
- Myelofibrosis with myeloid metaplasia (MMM) is linked to the reactivation of embryonic blood formation sites.
Purpose of the Study:
- To evaluate the extent of splenic hematopoiesis (myelopoiesis) in human fetuses.
- To investigate the role of the fetal spleen in blood cell development in relation to MMM pathophysiology.
Main Methods:
- Studied spleens from 48 fetuses and stillborn infants.
- Utilized immunohistologic and cytochemical techniques to identify hematopoietic cells.
- Focused on granulocytic, erythroid, and megakaryocytic cell identification.
Main Results:
- Found minimal evidence of active hematopoiesis in the fetal spleen.
- Detected virtually no hematopoietic cells within the dividing cell pool.
- Observed that identified immature cells likely represent trapped circulating precursors.
Conclusions:
- The human fetal spleen is not a major site of active hematopoiesis.
- Findings suggest fetal splenic hematopoietic cells are primarily trapped precursors.
- These results have implications for understanding the pathophysiology of myelofibrosis with myeloid metaplasia (MMM).
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