Cellular immune responses in amniotic fluid of women with preterm prelabor rupture of membranes
Abstract
Background: Preterm birth is the leading cause of perinatal morbidity and mortality. Preterm prelabor rupture of membranes (pPROM) occurs in 30% of preterm births; thus, this complication is a major contributor to maternal and neonatal morbidity. However, the cellular immune responses in amniotic fluid of women with pPROM have not been investigated. Methods: Amniotic fluid samples were obtained from women with pPROM and a positive (n = 7) or negative (n =10) microbiological culture. Flow cytometry was performed to evaluate the phenotype and number of amniotic fluid leukocytes. The correlation between amniotic fluid immune cells and an interleukin-6 (IL-6) concentration or a white blood cell (WBC) count in amniotic fluid was calculated. Results: Women with pPROM and a positive amniotic fluid culture had (1) a greater number of total leukocytes in amniotic fluid, including neutrophils and monocytes/macrophages and (2) an increased number of total T cells in amniotic fluid, namely CD4+ T cells and CD8+ T cells, but not B cells. The numbers of neutrophils and monocytes/macrophages were positively correlated with IL -6 concentrations and WBC counts in amniotic fluid of women with pPROM. Conclusion: Women with pPROM and a positive amniotic fluid culture exhibit a more severe cellular immune response than those with a negative culture, which is associated with well-known markers of intra-amniotic inflammation.
Más información
| Título según WOS: | Cellular immune responses in amniotic fluid of women with preterm prelabor rupture of membranes |
| Título según SCOPUS: | Cellular immune responses in amniotic fluid of women with preterm prelabor rupture of membranes |
| Título de la Revista: | JOURNAL OF PERINATAL MEDICINE |
| Volumen: | 48 |
| Número: | 3 |
| Editorial: | WALTER DE GRUYTER GMBH |
| Fecha de publicación: | 2020 |
| Página de inicio: | 222 |
| Página final: | 233 |
| Idioma: | English |
| DOI: |
10.1515/jpm-2019-0395 |
| Notas: | ISI, SCOPUS |