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Increased serum level of vascular endothelial growth factor in Mycobacterium avium complex infection
Author(s) -
NISHIGAKI Yutaka,
FUJIUCHI Satoru,
FUJITA Yuka,
YAMAZAKI Yasuhiro,
SATO Maki,
YAMAMOTO Yasushi,
TAKEDA Akinori,
FUJIKANE Toshiaki,
SHIMIZU Tetsuo,
KIKUCHI Kenjiro
Publication year - 2006
Publication title -
respirology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 85
eISSN - 1440-1843
pISSN - 1323-7799
DOI - 10.1111/j.1440-1843.2006.00863.x
Subject(s) - medicine , pathogenesis , vascular endothelial growth factor , mycobacterium avium complex , immunohistochemistry , pathology , lung , immunology , gastroenterology , vegf receptors
Objective: Pulmonary infection caused by Mycobacterium avium complex (MAC) is one of the granulomatous diseases which are associated with the expression of vascular endothelial growth factor (VEGF). The aim of the present study was to clarify the association of VEGF with the pathogenesis of MAC infection. Methodology: The serum VEGF levels in 46 patients with pulmonary MAC infection were compared with those in 16 normal control subjects. Pulmonary lesions were evaluated using chest CT. In 20 patients, after treatment, serum VEGF levels were measured and chest CT performed again to evaluate pulmonary response to treatment. Results: Infected patients had higher serum VEGF levels than controls (435.2 ± 29.1 vs. 167.0 ± 10.6 pg/mL, P < 0.0001), and serum VEGF level correlated with the extent of disease. The serum VEGF levels in 14 patients who underwent treatment and exhibited an improvement in their pulmonary lesions decreased significantly compared with the results pretreatment (509.0 ± 60.7 vs. 303.6 ± 65.3 pg/mL, P = 0.0092). In infected patients, alveolar macrophages, epithelioid cells and multinucleated giant cells exhibited VEGF overexpression on immunohistochemical staining. Conclusions: This study suggests that VEGF may be associated with the pathogenesis of pulmonary MAC infection. Additionally, serum VEGF levels may be a useful surrogate marker for evaluating the extent of disease and of the response to treatment.