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Published on: June 24, 2020
Preterm Birth Therapies to Target Inflammation
Ioannis Pavlidis1, Sarah J Stock2
1University of Warwick Biomedical Research Unit in Reproductive Health, Coventry, UK.
Insights
Preterm birth (PTB) prevention and treatment remain challenging due to limited therapies. Targeting inflammation in gestational tissues offers promising new strategies for managing PTB and its complications.
Area of Science:
- Reproductive biology
- Immunology
- Perinatology
Background:
- Preterm birth (PTB) is a leading cause of infant mortality.
- Limited therapeutic options exist for PTB prevention and treatment.
- Inflammation in gestational tissues is a key factor in PTB pathophysiology.
Purpose of the Study:
- To review current and emerging therapeutic strategies for PTB.
- To discuss therapies targeting inflammatory pathways involved in PTB.
Main Methods:
- Review of traditional therapies for PTB.
- Highlighting novel preclinical approaches targeting inflammatory mediators.
- Discussion of mechanistic studies on PTB pathophysiology.
Main Results:
- Inflammation, even without infection, can trigger parturition.
- Several therapeutic targets within inflammatory pathways have been identified.
- Both established and novel therapeutic approaches show potential.
Conclusions:
- Effective PTB prevention and treatment strategies are urgently needed.
- Targeting inflammation offers a promising avenue for PTB management.
- Collaborative efforts are essential to address the challenge of PTB.
Abstract:
Preterm birth (PTB; defined as delivery before 37 weeks of pregnancy) is the leading cause of morbidity and mortality in infants and children aged <5 years, conferring potentially devastating short- and long-term complications. Despite extensive research in the field, there is currently a paucity of medications available for PTB prevention and treatment. Over the past few decades, inflammation in gestational tissues has emerged at the forefront of PTB pathophysiology. Even in the absence of infection, inflammation alone can prematurely activate the main components of parturition resulting in uterine contractions, cervical ripening and dilatation, membrane rupture, and subsequent PTB. Mechanistic studies have identified critical elements of the complex inflammatory molecular pathways involved in PTB. Here, we discuss therapeutic options that target such key mediators with an aim to prevent, postpone, or treat PTB. We provide an overview of more traditional therapies that are currently used or being tested in humans, and we highlight recent advances in preclinical studies introducing novel approaches with therapeutic potential. We conclude that urgent collaborative action is required to address the unmet need of developing effective strategies to tackle the challenge of PTB and its complications.
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