Hepatitis C virus (HCV) infects approximately 20-40% of the millions of incarcerated individuals in the United States. While many studies have characterized the seroincidence of chronic HCV infection, none have specifically addressed the issue of acute HCV infection. Since incarceration is associated with new onset intravenous drug use, such individuals would be at high risk for acute HCV infection. Screening of high-risk populations will shed insight into the incidence and clinical course of individuals and allow for characterization of their immune responses. Moreover, treatment outcomes for HCV are far better when treating early in infection, therefore identification of individuals with acute HCV is of extreme clinical benefit due to the greatly enhanced possibility of viral eradication. Interventions such as counseling, safe-needle techniques, and immunizations against hepatitis A and hepatitis B virus are also necessary. Without any systematic approach, preliminary efforts have identified 19 cases of acute HCV identified from 2 populations of incarcerated individuals over a 30-month period. This project aims to improve the identification of such subjects within the Massachusetts correctional system, describe their clinical courses, while providing access to counseling, education, and treatment for the identified individuals. Individuals identified in the correctional system uniquely complement the Brazilian cohort, since acute HCV associated with IVDU is not a frequent occurrence in our Brazilian patients. Moreover, we aim to analyze differences that explore the influence of race on the presentation of HCV. Therefore, the two cohorts will allow us to address the impact of risk factor for HCV acquisition on the immunology of acute HCV infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI066345-02
Application #
7310370
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
2
Fiscal Year
2006
Total Cost
$124,812
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Yu, Wen-Han; Cosgrove, Cormac; Berger, Christoph T et al. (2018) ADCC-Mediated CD56DIM NK Cell Responses Are Associated with Early HBsAg Clearance in Acute HBV Infection. Pathog Immun 3:2-18
Forconi, Catherine S; Cosgrove, Cormac P; Saikumar-Lakshmi, Pryia et al. (2018) Poorly cytotoxic terminally differentiated CD56negCD16pos NK cells accumulate in Kenyan children with Burkitt lymphomas. Blood Adv 2:1101-1114
Torres-Cornejo, Almudena; Lauer, Georg M (2017) Hurdles to the Development of Effective HBV Immunotherapies and HCV Vaccines. Pathog Immun 2:102-125
Vergara, C; Thio, C; Latanich, R et al. (2017) Genetic basis for variation in plasma IL-18 levels in persons with chronic hepatitis C virus and human immunodeficiency virus-1 infections. Genes Immun 18:82-87
Wolski, David; Foote, Peter K; Chen, Diana Y et al. (2017) Early Transcriptional Divergence Marks Virus-Specific Primary Human CD8+ T Cells in Chronic versus Acute Infection. Immunity 47:648-663.e8
Rodrigo, Chaturaka; Walker, Melanie R; Leung, Preston et al. (2017) Limited naturally occurring escape in broadly neutralizing antibody epitopes in hepatitis C glycoprotein E2 and constrained sequence usage in acute infection. Infect Genet Evol 49:88-96
Rodrigo, C; Eltahla, A A; Bull, R A et al. (2017) Phylogenetic analysis of full-length, early infection, hepatitis C virus genomes among people with intravenous drug use: the InC3 Study. J Viral Hepat 24:43-52
Rodrigo, Chaturaka; Eltahla, Auda A; Bull, Rowena A et al. (2016) Historical Trends in the Hepatitis C Virus Epidemics in North America and Australia. J Infect Dis 214:1383-1389
Page, Kimberly; Mirzazadeh, Ali; Rice, Thomas M et al. (2016) Interferon Lambda 4 Genotype Is Associated With Jaundice and Elevated Aminotransferase Levels During Acute Hepatitis C Virus Infection: Findings From the InC3 Collaborative. Open Forum Infect Dis 3:ofw024
Gunn, Bronwyn; Schneider, Jeffrey; Shansab, Maryam et al. (2016) Enhanced binding of antibodies generated during chronic HIV infection to mucus component MUC16. Mucosal Immunol 9:1549-1558

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