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The Th-17 response and its potential role in post-injury pulmonary complications
Travis L Holloway1, Martin G Schwacha
1Department of Surgery, Division of Trauma and Emergency Surgery, The University of Texas Health Science Center San Antonio, TX 78229.
Insights
Trauma can cause acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Investigating T-helper 17 (Th-17) cells and IL-17 may reveal new treatments for post-trauma lung complications.
Area of Science:
- Immunology
- Critical Care Medicine
- Public Health
Background:
- Trauma is a significant cause of death and illness, often leading to costly ICU stays due to complications like acute lung injury (ALI) and acute respiratory distress syndrome (ARDS).
- The precise mechanisms underlying trauma-related lung injury remain unclear, despite improvements in care.
- Inflammatory processes, particularly those involving T-helper 17 (Th-17) cells and their cytokine IL-17, are implicated in lung injury and inflammatory diseases.
Purpose of the Study:
- To explore the role of the novel T-helper 17 (Th-17) cell response in the pathogenesis of trauma-induced acute lung injury (ALI) and acute respiratory distress syndrome (ARDS).
- To investigate the potential of Th-17 cells and IL-17 as biomarkers and therapeutic targets for post-traumatic lung complications.
Main Methods:
- Review of current evidence on inflammatory cascades in trauma-related lung injury.
- Examination of the role of T-helper cell subsets, specifically Th-17, in non-traumatic and inflammatory lung diseases.
- Proposal for utilizing findings from animal models and human trauma victims' cytokine profiles.
Main Results:
- Current evidence points to a pro-inflammatory cascade in trauma-related lung injury.
- A novel T-cell response involving Th-17 cells and IL-17 is increasingly recognized in inflammatory lung diseases.
- This Th-17 pathway presents a potential avenue for understanding ALI and ARDS pathogenesis.
Conclusions:
- The Th-17 cell pathway and IL-17 cytokine represent a promising area for further research into the mechanisms of ALI and ARDS following trauma.
- Understanding these specific immune responses could lead to the development of novel therapeutic strategies for preventing and treating ARDS in trauma patients.
Abstract:
Trauma is a leading cause of death and morbidity among all ages and constitutes a major public health problem. This burden is initially directed at stabilizing direct injury, however, post-trauma complications are common and prolong costly ICU stays. Among these complications are acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). While care for these pulmonary complications has now been standardized and prevention continues to improve, the true pathophysiology has not been elucidated. Current evidence suggests that the activation of a pro-inflammatory cascade plays an important role in the pathogenesis of trauma related lung injury. Additionally, there is a novel T-cell response that has been shown to be intricately involved in other non-traumatic lung diseases and multiple inflammatory diseases. With the recent discovery of this novel T-helper subset (Th-17) and the main effector cytokine, IL-17, there is the potential for further categorizing the biologic mechanism leading to ALI and ARDS. By utilizing the discoveries provided by animal models and further investigation into local and systemic cytokine profiles in human trauma victims, the information gained holds promise in the development of unique therapeutic modalities for the treatment and prevention of ARDS following traumatic injury.
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