Lung Injury in Vivax Malaria: Pathophysiological Evidence for Pulmonary Vascular Sequestration and Posttreatment Alveolar-Capillary Inflammation

• Published in: The Journal of infectious diseases Vol. 195; no. 4; pp. 589 - 596
• Main Authors: Anstey, Nicholas M., Handojo, Tjandra, Pain, Michael C. F., Kenangalem, Enny, Tjitra, Emiliana, Price, Ric N., Maguire, Graeme P.
• Format: Journal Article
• Language: English
• Published: Chicago, IL The University of Chicago Press 15-02-2007; University of Chicago Press
• Subjects: Adolescent; Adult; Animals; Biological and medical sciences; Blood Gas Analysis; Capillaries - parasitology; Cough; Erythrocytes - parasitology; Falciparum malaria; Female; Fundamental and applied biological sciences. Psychology; Human protozoal diseases; Humans; Indonesia; Infectious diseases; Longitudinal Studies; Lung - blood supply; Lung - parasitology; Lung - pathology; Lung - physiopathology; Lung injury; Lungs; Malaria; Malaria, Falciparum - drug therapy; Malaria, Falciparum - parasitology; Malaria, Falciparum - pathology; Malaria, Falciparum - physiopathology; Malaria, Vivax - drug therapy; Malaria, Vivax - parasitology; Malaria, Vivax - pathology; Malaria, Vivax - physiopathology; Male; Medical sciences; Microbiology; Middle Aged; Oxygen; Oxygen - analysis; Parasitemia; Parasites; Parasitic diseases; Parasitism; Plasmodium vivax - physiology; Protozoal diseases; Pulmonary alveoli; Pulmonary Alveoli - pathology; Pulmonary Gas Exchange; Respiratory Function Tests; Respiratory Mechanics; Vivax malaria; Indonesia; Vascular disease; Infection; Lung disease; Protozoal disease; Microbiology; Malaria; Respiratory disease; Malformation; Pulmonary sequestration; Cardiovascular disease; Inflammation; Parasitosis
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1086/510756

Background. The mechanisms underlying lung injury in vivax malaria are not well understood. Inflammatory responses to Plasmodium falciparum and P. vivax, to our knowledge, have not previously been compared at an organ level. Methods. Respiratory symptoms and physiological aspects were measured longitudinally in Indonesian adults with uncomplicated vivax (n=50) and falciparum (n=50) malaria. Normal values were derived from 109 control subjects. Gas transfer was partitioned into its alveolar-capillary membrane (DM) and pulmonary capillary vascular (VC) components, to characterize the site and timing of impaired gas transfer. Results. Mean baseline VC volume was significantly reduced in vivax and falciparum malaria, improving with treatment in each species. Baseline DM function was not impaired in either species. The progressive deterioration in DM function after treatment was statistically significant in vivax malaria but not in uncomplicated falciparum malaria. Oxygen saturation deteriorated after treatment in vivax but improved in falciparum malaria. Conclusions. The baseline reduction in VC volume but not in DM function suggests encroachment on VC volume by parasitized erythrocytes and suggests that P. vivax-infected erythrocytes may sequester within the pulmonary microvasculature. Progressive alveolar-capillary dysfunction after treatment of vivax malaria is consistent with a greater inflammatory response to a given parasite burden in P. vivax relative to that in P. falciparum.