“…In the current study, we showed that the number of neutrophils in amniotic fluid is significantly higher in women with pPROM and a positive microbiological culture than in those without culturable microorganisms. Studies investigating the functions of amniotic fluid neutrophils have shown that these innate immune cells can phagocytize bacteria invading the amniotic cavity [67], form neutrophil extracellular traps (NETs) [68], and may degranulate, releasing anti-microbial molecules such as myeloperoxidase [69][70][71], alpha-defensins [70,[72][73][74], elastase [70,75,76], cathepsin G [70,77], lactoferrin [78], pentraxin-3 [79], and cathelicidin [69,70] as well as reactive oxygen species [80] into the amniotic cavity. In addition to participating in the host defense response to microbes, neutrophils can also release pro-inflammatory cytokines such as IL-8, tumor necrosis factor-α (TNF-α), macrophage inflammatory protein-1α (MIP-1α), MIP-1β, IL-1α, and IL-1β, which are implicated in the mechanisms leading to premature labor in the context of intra-amniotic infection [52,53,[81][82][83][84][85][86][87][88][89][90][91][92][93][94].…”