Preterm birth and sustained inflammation: consequences for the neonate
Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-235019
- Almost half of all preterm births are caused or triggered by an inflammatory process at the feto-maternal interface resulting in preterm labor or rupture of membranes with or without chorioamnionitis (“first inflammatory hit”). Preterm babies have highly vulnerable body surfaces and immature organ systems. They are postnatally confronted with a drastically altered antigen exposure including hospital-specific microbes, artificial devices, drugs, nutritional antigens, and hypoxia or hyperoxia (“second inflammatory hit”). This is of particularAlmost half of all preterm births are caused or triggered by an inflammatory process at the feto-maternal interface resulting in preterm labor or rupture of membranes with or without chorioamnionitis (“first inflammatory hit”). Preterm babies have highly vulnerable body surfaces and immature organ systems. They are postnatally confronted with a drastically altered antigen exposure including hospital-specific microbes, artificial devices, drugs, nutritional antigens, and hypoxia or hyperoxia (“second inflammatory hit”). This is of particular importance to extremely preterm infants born before 28 weeks, as they have not experienced important “third-trimester” adaptation processes to tolerate maternal and self-antigens. Instead of a balanced adaptation to extrauterine life, the delicate co-regulation between immune defense mechanisms and immunosuppression (tolerance) to allow microbiome establishment is therefore often disturbed. Hence, preterm infants are predisposed to sepsis but also to several injurious conditions that can contribute to the onset or perpetuation of sustained inflammation (SI). This is a continuing challenge to clinicians involved in the care of preterm infants, as SI is regarded as a crucial mediator for mortality and the development of morbidities in preterm infants. This review will outline the (i) role of inflammation for short-term consequences of preterm birth and (ii) the effect of SI on organ development and long-term outcome.…
Autor(en): | Alexander Humberg, Ingmar Fortmann, Bastian Siller, Matthias Volkmar Kopp, Egbert Herting, Wolfgang Göpel, Christoph Härtel |
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URN: | urn:nbn:de:bvb:20-opus-235019 |
Dokumentart: | Artikel / Aufsatz in einer Zeitschrift |
Institute der Universität: | Medizinische Fakultät / Kinderklinik und Poliklinik |
Sprache der Veröffentlichung: | Englisch |
Titel des übergeordneten Werkes / der Zeitschrift (Englisch): | Seminars in Immunopathology |
ISSN: | 1863-2297 |
Erscheinungsjahr: | 2020 |
Band / Jahrgang: | 42 |
Seitenangabe: | 451-468 |
Originalveröffentlichung / Quelle: | Seminars in Immunopathology (2020) 42:451–468. https://doi.org/10.1007/s00281-020-00803-2 |
DOI: | https://doi.org/10.1007/s00281-020-00803-2 |
Allgemeine fachliche Zuordnung (DDC-Klassifikation): | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Freie Schlagwort(e): | chronic pulmonary insufficiency of prematurity; microbiome; neurocognitive outcome; preterm infants; sepsis; sustained inflammation |
Datum der Freischaltung: | 10.06.2021 |
Urhebende Körperschaft: | German Neonatal Network, German Center for Lung Research and Priming Immunity at the beginning of life (PRIMAL) Consortium |
Lizenz (Deutsch): | CC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International |