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Antimicrobial Agents and Chemotherapy, June 2008, p. 2169-2174, Vol. 52, No. 6
0066-4804/08/$08.00+0 doi:10.1128/AAC.01506-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

í Salát,*
Ji
í Jelínek,
Jind
ich Chmela
, and
Jan Kopeck
Biology Centre Academy of Sciences of the Czech Republic, Institute of Parasitology and Faculty of Biological Sciences, University of South Bohemia,
eské Bud
jovice, Czech Republic
Received 20 November 2007/ Returned for modification 19 December 2007/ Accepted 11 March 2008
Microsporidia are eukaryotic, obligate, intracellular protists that are emerging pathogens in immunocompromised hosts, including AIDS patients and organ transplant recipients. The efficacy of gamma interferon (IFN-
) for the treatment of microsporidiosis caused by Encephalitozoon cuniculi was studied by means of adoptive transfer and IFN-
administration in SCID mice. While the adoptive transfer of CD4+ T cells from immunocompetent mice prolonged survival of SCID mice infected perorally with E. cuniculi, survival was not improved by adoptive transfer of CD4+ T lymphocytes from IFN-
-deficient mice. The protective effect of IFN-
was confirmed in cytokine therapy experiments in which SCID mice receiving IFN-
survived significantly longer than mice receiving mock injections. The administration of serum containing specific antibodies against E. cuniculi was found to prolong the survival of concurrently IFN-
-treated SCID mice. The data presented in this study suggest that IFN-
is potentially useful as a cytokine therapy for microsporidiosis, especially in CD4+ T-cell-deficient patients.
í Salát, Institute of Parasitology, Biology Centre Academy of Sciences of the Czech Republic, Brani
ovská 31, 370 05
eské Bud
jovice, Czech Republic. Phone: 420 387 775 458. Fax: 420 385 310 388. E-mail: george{at}paru.cas.cz
Published ahead of print on 17 March 2008.
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