Pathogen-specific loss of host resistance in mice lacking the IFN-γ-inducible gene IGTP

Gregory A. Taylor(National Cancer Institute), Carmen M. Collazo(National Cancer Institute), George Yap(National Cancer Institute), Khuong B. Nguyen(National Cancer Institute), T A Gregorio(National Cancer Institute), Lynn S. Taylor(Van Andel Institute), Bryn Eagleson(National Cancer Institute), Lisa Secrest(National Cancer Institute), Eileen Southon(National Cancer Institute), Susan Reid(National Cancer Institute), Lino Tessarollo(National Cancer Institute), Mike Bray(Van Andel Institute), Daniel W. McVicar(Van Andel Institute), Kristin L. Komschlies(National Cancer Institute), Howard A. Young(Van Andel Institute), Christine A. Biron(Brown University), Alan Sher(National Cancer Institute), George F. Vande Woude(National Cancer Institute)
Proceedings of the National Academy of Sciences
January 18, 2000
Cited by 271Open Access

Abstract

Interferon-gamma (IFN-gamma) is critical for defense against pathogens, but the molecules that mediate its antimicrobial responses are largely unknown. IGTP is the prototype for a family of IFN-gamma-regulated genes that encode 48-kDa GTP-binding proteins that localize to the endoplasmic reticulum. We have generated IGTP-deficient mice and found that, despite normal immune cell development and normal clearance of Listeria monocytogenes and cytomegalovirus infections, the mice displayed a profound loss of host resistance to acute infections of the protozoan parasite Toxoplasma gondii. By contrast, IFN-gamma receptor-deficient mice have increased susceptibility to all three pathogens. Thus, IGTP defines an IFN-gamma-regulated pathway with a specialized role in antimicrobial resistance.


Related Papers

No related papers found

Powered by citation graph analysis