The purpose of this study is to develop a field-applicable assay for the detection of the liver fluke, Schistosoma mansoni. Rhesus monkeys experimentally infected with S. mansoni are the source of infection-related sera. This material will be used to identify schistosome-specific antigens. Once identified, these antigens will be used to develop specific diagnostic tests. In the previous 2 years 5 rhesus monkeys were infected with 300 S. mansoni cercariae. Blood and stool samples were collected bimonthly from the infected animals. At week 60 the animals were treated with Droncit and samples continued to be collected following treatment. Ultimately the animals were necropsied. The presence or absence of adult schistosomes was determined and quantified, if present. Some animals remained parasitemic although treated with a curative dose of Droncit. Immunological analysis of these serum samples for antibodies to S. mansoni showed that some animals were successfully trea ted. Studies during the past year focused on determining if antibody status reflects successful treatment. Preliminary evidence showed that antibody levels correlated to successful treatment in some monkeys. Related studies in humans have also been continuing. Human studies have focused on determining the risk of S. mansoni infection in persons traveling to Malawi and Ethiopia. Efforts are being made to differentiate treatment success or failure by monitoring changes in specific antibody responses to S. mansoni after treatment. Immunological analysis of these samples are currently in progress.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
3P51RR000165-37S1
Application #
2711858
Study Section
Project Start
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
37
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Claw, Katrina G; George, Renee D; MacCoss, Michael J et al. (2018) Quantitative evolutionary proteomics of seminal fluid from primates with different mating systems. BMC Genomics 19:488
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Georgieva, Maria; Sia, Jonathan Kevin; Bizzell, Erica et al. (2018) Mycobacterium tuberculosis GroEL2 Modulates Dendritic Cell Responses. Infect Immun 86:
Tedesco, Dana; Grakoui, Arash (2018) Environmental peer pressure: CD4+ T cell help in tolerance and transplantation. Liver Transpl 24:89-97
Mavigner, Maud; Habib, Jakob; Deleage, Claire et al. (2018) Simian Immunodeficiency Virus Persistence in Cellular and Anatomic Reservoirs in Antiretroviral Therapy-Suppressed Infant Rhesus Macaques. J Virol 92:
Walker, Lary C (2018) Prion-like mechanisms in Alzheimer disease. Handb Clin Neurol 153:303-319
Kamberov, Yana G; Guhan, Samantha M; DeMarchis, Alessandra et al. (2018) Comparative evidence for the independent evolution of hair and sweat gland traits in primates. J Hum Evol 125:99-105
Wakeford, Alison G P; Morin, Elyse L; Bramlett, Sara N et al. (2018) A review of nonhuman primate models of early life stress and adolescent drug abuse. Neurobiol Stress 9:188-198
Singh, Arun; Jenkins, Meagan A; Burke Jr, Kenneth J et al. (2018) Glutamatergic Tuning of Hyperactive Striatal Projection Neurons Controls the Motor Response to Dopamine Replacement in Parkinsonian Primates. Cell Rep 22:941-952

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