Wolska Magdalena, Wypych Tomasz Piotr, Rodríguez-Viso Pilar
Laboratory of Host-Microbiota Interactions, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Ludwika Pasteura 3, 02-093 Warsaw, Poland.
Metabolites. 2024 Jul 11;14(7):382. doi: 10.3390/metabo14070382.
Globally, around 11% of neonates are born prematurely, comprising a highly vulnerable population with a myriad of health problems. Premature births are often accompanied by an underdeveloped immune system biased towards a Th2 phenotype and microbiota dysbiosis. Typically, a healthy gut microbiota interacts with the host, driving the proper maturation of the host immunity. However, factors like cesarean section, formula milk feeding, hospitalization in neonatal intensive care units (NICU), and routine antibiotic treatments compromise microbial colonization and increase the risk of developing related diseases. This, along with alterations in the innate immune system, could predispose the neonates to the development of respiratory diseases later in life. Currently, therapeutic strategies are mainly focused on restoring gut microbiota composition using probiotics and prebiotics. Understanding the interactions between the gut microbiota and the immature immune system in premature neonates could help to develop novel therapeutic strategies for treating or preventing gut-lung axis disorders.
在全球范围内,约11%的新生儿早产,这是一个极易受到伤害且伴有众多健康问题的群体。早产常常伴随着免疫系统发育不全,偏向于Th2表型以及微生物群失调。通常,健康的肠道微生物群与宿主相互作用,推动宿主免疫的正常成熟。然而,剖宫产、配方奶喂养、新生儿重症监护病房(NICU)住院治疗以及常规抗生素治疗等因素会损害微生物定植,并增加患相关疾病的风险。这与先天免疫系统的改变一起,可能使新生儿在日后生活中更容易患上呼吸系统疾病。目前,治疗策略主要集中在使用益生菌和益生元来恢复肠道微生物群的组成。了解早产新生儿肠道微生物群与未成熟免疫系统之间的相互作用,有助于开发治疗或预防肠-肺轴疾病的新治疗策略。