“…G-CSF has been discussed as the causative agent for the occurrence of Sweet syndrome, leukocytoclastic vasculitis, interstitial pneumonitis, adult respiratory distress syndrome (ARDS), pyoderma gangraenosum, capillary leakage, stroke, acute gouty arthritis, iritis, severe anaphylactoid reactions, and non-traumatic rupture of the spleen. 11,[16][17][18][19][20][21][22][23][24] On the other hand, growth factors such as G-CSF and GM-CSF have been proven to reduce the incidence of documented infections in neutropenic patients and they have been shown to reduce the risk of pyogenic infections in patients with chronic granulomatous disease. 25 In contrast, by increasing the activity of the oxidative burst in neutrophils a pathophysiological role of these substances in augmenting inflammatory processes in persons or patients with normal or even subnormal neutrophil counts and/or function must be discussed (for summary see Spiekermann et al 16 ).…”