Details

Autor(en) / Beteiligte

• Kolawole, Elizabeth Motunrayo
• McLeod, Jamie Josephine Avila
• Ndaw, Victor
• Abebayehu, Daniel
• Barnstein, Brian O
• Faber, Travis
• Spence, Andrew J
• Taruselli, Marcela
• Paranjape, Anuya
• Haque, Tamara T
• Qayum, Amina A
• Kazmi, Qasim A
• Wijesinghe, Dayanjan S
• Sturgill, Jamie L
• Chalfant, Charles E
• Straus, David B
• Oskeritzian, Carole A
• Ryan, John J

Titel

Fluvastatin Suppresses Mast Cell and Basophil IgE Responses: Genotype-Dependent Effects

Ist Teil von

• The Journal of immunology (1950), 2016-02, Vol.196 (4), p.1461-1470

Ort / Verlag

United States

Erscheinungsjahr

2016

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Mast cell (MC)- and basophil-associated inflammatory diseases are a considerable burden to society. A significant portion of patients have symptoms despite standard-of-care therapy. Statins, used to lower serum cholesterol, have immune-modulating activities. We tested the in vitro and in vivo effects of statins on IgE-mediated MC and basophil activation. Fluvastatin showed the most significant inhibitory effects of the six statins tested, suppressing IgE-induced cytokine secretion among mouse MCs and basophils. The effects of fluvastatin were reversed by mevalonic acid or geranylgeranyl pyrophosphatase, and mimicked by geranylgeranyl transferase inhibition. Fluvastatin selectively suppressed key FcεRI signaling pathways, including Akt and ERK. Although MCs and basophils from the C57BL/6J mouse strain were responsive to fluvastatin, those from 129/SvImJ mice were completely resistant. Resistance correlated with fluvastatin-induced upregulation of the statin target HMG-CoA reductase. Human MC cultures from eight donors showed a wide range of fluvastatin responsiveness. These data demonstrate that fluvastatin is a potent suppressor of IgE-mediated MC activation, acting at least partly via blockade of geranyl lipid production downstream of HMG-CoA reductase. Importantly, consideration of statin use for treating MC-associated disease needs to incorporate genetic background effects, which can yield drug resistance.