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Items: 1 to 20 of 97

1.

Redundant and pathogenic roles for IL-22 in mycobacterial, protozoan, and helminth infections.

Wilson MS, Feng CG, Barber DL, Yarovinsky F, Cheever AW, Sher A, Grigg M, Collins M, Fouser L, Wynn TA.

J Immunol. 2010 Apr 15;184(8):4378-90. doi: 10.4049/jimmunol.0903416. Epub 2010 Mar 10.

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Toxoplasma gondii and Schistosoma mansoni synergize to promote hepatocyte dysfunction associated with high levels of plasma TNF-alpha and early death in C57BL/6 mice.

Marshall AJ, Brunet LR, van Gessel Y, Alcaraz A, Bliss SK, Pearce EJ, Denkers EY.

J Immunol. 1999 Aug 15;163(4):2089-97.

4.

Exacerbated susceptibility to infection-stimulated immunopathology in CD1d-deficient mice.

Smiley ST, Lanthier PA, Couper KN, Szaba FM, Boyson JE, Chen W, Johnson LL.

J Immunol. 2005 Jun 15;174(12):7904-11.

5.

IL-22 mediates host defense against an intestinal intracellular parasite in the absence of IFN-γ at the cost of Th17-driven immunopathology.

Stange J, Hepworth MR, Rausch S, Zajic L, Kühl AA, Uyttenhove C, Renauld JC, Hartmann S, Lucius R.

J Immunol. 2012 Mar 1;188(5):2410-8. doi: 10.4049/jimmunol.1102062. Epub 2012 Jan 20.

6.

Schistosome-infected IL-4 receptor knockout (KO) mice, in contrast to IL-4 KO mice, fail to develop granulomatous pathology while maintaining the same lymphokine expression profile.

Jankovic D, Kullberg MC, Noben-Trauth N, Caspar P, Ward JM, Cheever AW, Paul WE, Sher A.

J Immunol. 1999 Jul 1;163(1):337-42.

7.

Genetic control of severe egg-induced immunopathology and IL-17 production in murine schistosomiasis.

Smith PM, Shainheit MG, Bazzone LE, Rutitzky LI, Poltorak A, Stadecker MJ.

J Immunol. 2009 Sep 1;183(5):3317-23. doi: 10.4049/jimmunol.0901504. Epub 2009 Aug 12.

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Lack of C3 affects Th2 response development and the sequelae of chemotherapy in schistosomiasis.

La Flamme AC, MacDonald AS, Huxtable CR, Carroll M, Pearce EJ.

J Immunol. 2003 Jan 1;170(1):470-6.

11.

IL-23 is required for the development of severe egg-induced immunopathology in schistosomiasis and for lesional expression of IL-17.

Rutitzky LI, Bazzone L, Shainheit MG, Joyce-Shaikh B, Cua DJ, Stadecker MJ.

J Immunol. 2008 Feb 15;180(4):2486-95.

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Coinfection with the intestinal nematode Heligmosomoides polygyrus markedly reduces hepatic egg-induced immunopathology and proinflammatory cytokines in mouse models of severe schistosomiasis.

Bazzone LE, Smith PM, Rutitzky LI, Shainheit MG, Urban JF, Setiawan T, Blum AM, Weinstock JV, Stadecker MJ.

Infect Immun. 2008 Nov;76(11):5164-72. doi: 10.1128/IAI.00673-08. Epub 2008 Aug 18.

15.

IL-23 provides a limited mechanism of resistance to acute toxoplasmosis in the absence of IL-12.

Lieberman LA, Cardillo F, Owyang AM, Rennick DM, Cua DJ, Kastelein RA, Hunter CA.

J Immunol. 2004 Aug 1;173(3):1887-93.

17.

Differential regulation of nitric oxide synthase-2 and arginase-1 by type 1/type 2 cytokines in vivo: granulomatous pathology is shaped by the pattern of L-arginine metabolism.

Hesse M, Modolell M, La Flamme AC, Schito M, Fuentes JM, Cheever AW, Pearce EJ, Wynn TA.

J Immunol. 2001 Dec 1;167(11):6533-44.

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Expression of interleukin-9 leads to Th2 cytokine-dominated responses and fatal enteropathy in mice with chronic Schistosoma mansoni infections.

Fallon PG, Smith P, Richardson EJ, Jones FJ, Faulkner HC, Van Snick J, Renauld JC, Grencis RK, Dunne DW.

Infect Immun. 2000 Oct;68(10):6005-11.

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