Journal Article
Research Support, Non-U.S. Gov't
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Distribution of invariant natural killer T cells and dendritic cells in late pre-term birth without acute chorioamnionitis.

PROBLEM: Acute chorioamnionitis (aCAM) is an important cause of pre-term birth. However, little is known about the pathogenesis of late pre-term birth without aCAM that was the most common category of pre-term birth. Here we analyze the kinetics of immune cells obtained from the decidua of women with late pre-term births with and without aCAM.

METHOD OF STUDY: Deciduas were obtained from women who underwent labor with late pre-term birth without aCAM (PB-n/aCAM) or with aCAM (PB-w/aCAM). The population of DEC-205+ dendritic cells (DCs), macrophages, invariant natural killer T (iNKT) cells, NK cells, CD8+ T cells, and CD4+ T cells were analyzed by flow cytometry.

RESULTS: The number of iNKT cells was higher in the decidua obtained from women with PB-n/aCAM than PB-w/aCAM. DEC-205+ DCs obtained from women with PB-n/aCAM preferentially induced iNKT cell proliferation.

CONCLUSION: iNKT cell accumulation with DEC-205+ DCs in PB-n/aCAM suggests that iNKT cells contribute to the onset of PB-n/aCAM.

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