An in vitro and in vivo study of cytokines in the acute-phase response associated with bisphosphonates

• Published in: Calcified tissue international 1997-11, Vol.61 (5), p.386-392
• Main Authors: Thiébaud, D, Sauty, A, Burckhardt, P, Leuenberger, P, Sitzler, L, Green, J R, Kandra, A, Zieschang, J, Ibarra de Palacios, P
• Format: Article
• Language: English
• Subjects: Acute-Phase Reaction - blood; Acute-Phase Reaction - metabolism; Adult; Bone Diseases - blood; Bone Diseases - drug therapy; Carrier Proteins - metabolism; Clodronic Acid - administration & dosage; Clodronic Acid - therapeutic use; Diphosphonates - administration & dosage; Diphosphonates - therapeutic use; Female; Humans; Imidazoles - administration & dosage; Imidazoles - therapeutic use; Injections, Intravenous; Interleukin-1 - blood; Interleukin-6 - blood; Leukocyte Count - drug effects; Male; Middle Aged; Pamidronate; Tumor Necrosis Factor-alpha - analysis; Zoledronic Acid
• ISSN: 0171-967X; 1432-0827
• DOI: 10.1007/s002239900353

We studied the acute phase response, including specific cytokine production, [interleukin-1 (IL-1), interleukin-6 (IL-6), tumor necrosis factor alpha(TNF alpha)] following a single dose of Aredia (disodium pamidronate) in patients with increased bone turnover and, in vitro, the role played by specific cytokines in the acute-phase reaction which may follow the administration of aminobisphosphonates. An in vivo exploratory study was done on 24 in- and outpatients with increased bone turnover given a single intravenous dose of pamidronate 60 mg. Measurements were taken at baseline and at 24, 48, and 72 hours. The main outcome measures were changes from baseline in serum IL-1, IL-6, and TNF alpha. In addition, C-reactive protein (CRP), white blood cell count (WCC), lymphocyte count, and elastase concentration were measured. Symptomatic evaluation was made of fever, bone pain, and rigors. In vitro, whole blood from eight healthy volunteers was exposed to various concentrations of the three bisphosphonates--pamidronate, clodronate, and zoledronate. Measurements were taken immediately before and at 3, 6, and 10 hours after exposure to drugs. The main outcome measures were changes in serum IL-1, IL-6, and TNF alpha. In vivo, there was a statistically significant (P < 0.001) increase in median values of TNF alpha in all post-baseline measurements. Median values for IL-6 also showed a significant (P < 0.001) increase at 24 hours after dosing. There were no statistically significant changes in median IL-1 values. Few patients showed any change from baseline in total WCC or in lymphocyte count, but 62.5% of patients with normal range baseline values for CRP increased to above normal levels after treatment. Fourteen patients experienced fever; 2 reported rigors. There was no correlation between fever and changes in cytokines. There were no serious adverse experiences or premature discontinuations due to poor tolerability, and 91% of the patients expressed willingness to receive pamidronate again. In vitro, an increase in TNF alpha and a mild increase in IL-6 was seen with all bisphosphonates, with the greatest effects seen with the highest concentration of both pamidronate and zoledronate. No changes were observed in IL-1 with any agent. Significant changes in both TNF alpha and IL-6 were observed within 3 days of a single dose of pamidronate in patients treated for the first time confirming previous findings. However, the lack of change in IL-1 in vivo and in vitro do