Table 1.
Clinical effects of endothelial cell dysfunction during DV infection
| Organ | Effects on endothelium * | Clinical effect |
|---|---|---|
| Lung pleura | Increased vascular permeability | Pleural effusion |
| Lung alveoli | Increased vascular permeability | Haemoptysis |
| Pericardium | Increased vascular permeability | Pericardial effusion |
| Abdomen | Increased vascular permeability | Ascitis |
| Brain | Damaged blood–brain barrier | Encephalopathy |
| Gut | Increased vascular permeability | Haemoptysis, Malaena |
| Urinary tract | Increased vascular permeability | Haematuria |
| Female reproductive tract | Increased vascular permeability | Menorrhagia, bleeding per vaginum |
The release of cytokines and other mediators released by activation of memory T cells acts on endothelium, resulting mainly in opening up of junctions between endothelial cells, thus increasing permeability.