Abstract
Alveolar macrophage (AM) responses are commonly induced in inhalation toxicology studies, typically being observed as an increase in number or a vacuolated 'foamy' morphology. Discriminating between adaptive AM responses and adverse events during nonclinical and clinical development is a major scientific challenge. When measuring and interpreting induced AM responses, an understanding of macrophage biology is essential; this includes 'sub-types' of AMs with different roles in health and disease and mechanisms of induction/resolution of AM responses to inhalation of pharmaceutical aerosols. In this context, emerging assay techniques, the utility of toxicokinetics and the requirement for new biomarkers are considered. Risk assessment for nonclinical toxicology findings and their translation to effects in humans is discussed from a scientific and regulatory perspective. At present, when apparently adaptive macrophage-only responses to inhaled investigational products are observed in nonclinical studies, this poses a challenge for risk assessment and an improved understanding of induced AM responses to inhaled pharmaceuticals is required.
| Original language | English |
|---|---|
| Pages (from-to) | 15-33 |
| Number of pages | 19 |
| Journal | Advanced Drug Delivery Reviews |
| Volume | 71 |
| DOIs | |
| Publication status | Published - May 2014 |
| Externally published | Yes |
Austrian Fields of Science 2012
- 301211 Toxicology
Keywords
- Drug delivery
- Inhalation
- Nonclinical
- Regulatory toxicology
- Respiratory
- Safety
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