This project's long-term aim is to gain understanding of immune responses in cysticercosis, with a view to develop novel immunotherapies. Cysticercosis, due to invasion of the pork tapeworm larvae Taenia solium, is an emerging disease in wealthier nations and a major cause of morbidity in endemic areas including South America and India. Epilepsy is the most prominent clinical manifestation and is due to parasitic cysticerci in the central nervous system (CNS). In the USA, cysticercosis is increasingly common in part because of the influx of immigrants. The initial pathological response in cysticercosis is the formation of eosinophil-rich inflammatory granulomas. Drug treatment may eliminates cysts but is associated with transient leukocyte influx into the CNS leading to clinical deterioration and sometimes death. In order to develop novel therapeutic strategies and to limit cellular influx, information is required about immune responses to this infection. There have been very few previous studies. On the basis of preliminary observations, the aim of this project is to collect in vivo data from patients (plus controls) on the presence of proinflammatory and chemotactic cytokines in infected patients. Such cytokines are critical in initiating successful immunity and in controlling cellular influx to sites of infection. We shall measure by ELISA, cytokine concentrations in plasma and cerebrospinal fluid. The ability of patient leukocytes to express genes for (northern analysis) and secrete such cytokines will be determined. Patterns of cytokine secretion during treatment will be examined to determine if anti- cytokine therapies are a real possibility. Finally, pilot work will develop an in vitro model of infection examining interactions between cysticerci and macrophages. The information will provide essential data needed to understand immunity to cysticercosis and for development of new treatments.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
1R03AI042037-01
Application #
2440548
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Project Start
1998-09-30
Project End
2001-08-31
Budget Start
1998-09-30
Budget End
1999-08-31
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
U of L Royal Postgraduate Medical School
Department
Type
DUNS #
City
London
State
Country
United Kingdom
Zip Code
Uddin, Jasim; Gonzalez, Armando E; Gilman, Robert H et al. (2010) Mechanisms regulating monocyte CXCL8 secretion in neurocysticercosis and the effect of antiparasitic therapy. J Immunol 185:4478-84
Uddin, Jasim; Gonzalez, Armando E; Gilman, Robert H et al. (2006) Neurocysticercal antigens stimulate chemokine secretion from human monocytes via an NF-kappaB-dependent pathway. Microbes Infect 8:1732-40
Uddin, Jasim; Garcia, Hector H; Gilman, Robert H et al. (2005) Monocyte-astrocyte networks and the regulation of chemokine secretion in neurocysticercosis. J Immunol 175:3273-81
Garcia, H H; Gonzalez, A E; Gilman, R H et al. (2002) Circulating parasite antigen in patients with hydrocephalus secondary to neurocysticercosis. Am J Trop Med Hyg 66:427-30
Garcia, H H; Parkhouse, R M; Gilman, R H et al. (2000) Serum antigen detection in the diagnosis, treatment, and follow-up of neurocysticercosis patients. Trans R Soc Trop Med Hyg 94:673-6