Young injection drug users (IDU) constitute a distinctive high risk and understudied group with high rates of hepatitis C virus (HCV) infection. Our group has successfully initiated prospective research to identify and study early HCV infection in this population: we have enrolled 163 HCV antibody (anti-HCV) negative young IDU in a longitudinal study (UFO-3 Study) and identified 22 incident HCV infections, 19 of whom are being followed prospectively (Acute UFO study). Using transcription mediated amplification (TMA) testing we successfully detect acute HCV infection (10 of 22 new infections) during the seronegative window period. HCV incidence is estimated at 27.8% to 40.7% per year. 1 of 7 (14%) new genotype 1 HCV infections with completed RNA tests six months apart has spontaneously resolved infection and liver function tests (LFT) as measured by liver transaminase (ALT) levels are normal. 2 of 8 (25%) genotype 3 infections appear to be resolving. Preliminary immunological analyses have shown broad HCV-specific T cell responses in resolvers. This application seeks a 4-year renewal of NIDA R01 DAI 6017-01 to continue our investigation of immunological and viral factors related to resolution. We will continue immunological studies of the spectrum of cytotoxic T lymphocyte (CTL) responses and evolution within CTL targets (""""""""epitopes"""""""") in early infection, to identify early correlates of viral resolution, critical for defining correlates of protective immunity and thus future vaccine development. We will now include genotype 3 infection in these analyses. We will expand our investigation of factors that may be associated with determining candidacy for early antiviral treatment. Finally, we add to this application, a distinctive new study, incorporating epidemiological and molecular virology methods to study HCV infectivity and transmission dynamics of acute HCV between young IDU in injecting and sexual partnerships using phylogenetic analyses coupled with epidemiologic data. The team of investigators collaborating on this application combines the scientific disciplines of epidemiology, immunology, molecular virology, laboratory science and the clinical disciplines of hepatology and infectious disease in this study of acute HCV infection in young IDU.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA016017-04
Application #
7082097
Study Section
Special Emphasis Panel (ZRG1-HOP-N (90))
Program Officer
Comolli, Jean C
Project Start
2002-09-25
Project End
2009-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
4
Fiscal Year
2006
Total Cost
$505,801
Indirect Cost
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Morris, Meghan D; Montgomery, Martha E; Briceno, Alya et al. (2018) A Study of Sexual Relationship Power among Young Women Who Inject Drugs and Their Sexual Partners. Subst Use Misuse 53:1281-1287
Esmaeili, Aryan; Mirzazadeh, Ali; Morris, Meghan D et al. (2018) The Effect of Female Sex on Hepatitis C Incidence Among People Who Inject Drugs: Results From the International Multicohort InC3 Collaborative. Clin Infect Dis 66:20-28
Mirzazadeh, Ali; Evans, Jennifer L; Hahn, Judith A et al. (2018) Continued Transmission of HIV Among Young Adults Who Inject Drugs in San Francisco: Still Room for Improvement. AIDS Behav 22:1383-1394
Morris, Meghan D; Shiboski, Stephen; Bruneau, Julie et al. (2017) Geographic Differences in Temporal Incidence Trends of Hepatitis C Virus Infection Among People Who Inject Drugs: The InC3 Collaboration. Clin Infect Dis 64:860-869
Page, Kimberly; Yu, Michelle; Cohen, Jennifer et al. (2017) HCV screening in a cohort of HIV infected and uninfected homeless and marginally housed women in San Francisco, California. BMC Public Health 17:171
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
Esmaeili, A; Mirzazadeh, A; Carter, G M et al. (2017) Higher incidence of HCV in females compared to males who inject drugs: A systematic review and meta-analysis. J Viral Hepat 24:117-127
Page, Kimberly; Leeman, Lawrence; Bishop, Steven et al. (2017) Hepatitis C Cascade of Care Among Pregnant Women on Opioid Agonist Pharmacotherapy Attending a Comprehensive Prenatal Program. Matern Child Health J 21:1778-1783
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

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