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HIV and Hepatitis C Co-infection. Amy Kindrick, M.D., M.P.H. San Francisco AIDS ETC National HIV/AIDS Clinical Consultation Center. February 12, 2002. The Hepatitis C Virus. Is There Only One Kind of Hepatitis?. HCV Infection: Epidemiology. Major healthcare problem worldwide
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HIV and Hepatitis C Co-infection Amy Kindrick, M.D., M.P.H. San Francisco AIDS ETC National HIV/AIDS Clinical Consultation Center February 12, 2002
HCV Infection: Epidemiology • Major healthcare problem worldwide • 70%–90% of HCV-infected patients develop chronic disease • ~50 million infected worldwide • ~5 million in Europe • ~4 million in USA • Contributes to ~12,000 deaths/yr
<1 % 1–2.4 % 2.5–4.9 % 5–10 % > 10 % No data available HCV Has Broad Global Prevalence
Hepatitis C Virus Infection • U.S. Overall antibody prevalence 1.8% • 64% positive for HCV RNA • Estimated 2.7 million persons chronically infected • Parenteral transmission route • Current risk of transfusion about 1 in 1,000,000
How Is HCV Transmitted? • Infected blood • Needlestick • Needle sharing • Transfusion • ?Infected body fluids • Amniotic fluid • Breast milk
Who Should Be Tested? • Drug users • Recipients of blood products or organ transplant before 1992 • Long-term partners of infected individuals • Persons with occupational exposures • Children born to HCV-infected mothers • HIV-infected individuals
Consider Testing For • Persons with tattoos or body piercing • Persons with multiple sexual partners • Tissue transplant recipients
HCV Diagnosis • Enzyme immunoassays (EIA) • Initial screening test for patients with liver disease • False positives in low risk patients • Occasional false negatives, esp. With HIV+ • Recombinant immunoblot assays (RIBA) • Confirmatory test if EIA positive in low risk pt • HCV RNA by PCR • Confirmatory if RIBA is “indeterminant”
Hepatitis C Virus Infection: Diagnosis • HCV antibody • HCV viral load • HCV genotype • Liver function tests • Liver biopsy is gold standard for assessing disease status • ALT and AST do not predict liver histology • HCV RNA does not predict liver histology or outcomes
Hepatitis C Virus Infection • Incubation period 2-26 weeks • Acute infection may be asymptomatic • Natural history variable • Chronic infection in 70-75% • Cirrhosis in 10% to 20% of chronically infected • Develops in 15-25 years • Hepatocelluar carcinoma in 1% to 5% after 20 years • 1% to 4% per year once cirrhosis is established • Extrahepatic manifectations • Arthritis • Glomerulonephritis • Mixed cryoglobulinemia
HCV/HIV Co-infection:General Issues • U.S. Prevalence 40% to 60% • Varies geographically • Varies by HIV risk behavior • Major transmission routes are transfusion and IDU • Sexual and vertical transmission are rare • Coinfection may enhance • Sexual transmission of HIV • Vertical transmission of HCV
Diagnosis of HCV in HIV-infected Patients • Co-infection may reduce sensitivity of HCV antibody test (EIA or RIBA) • Measure HCV RNA by PCR or bDNA if history or clinical symptoms are suggestive
Patients With HCV and HIV: Key Points • 30% of patients with HIV also have HCV • Mortality from HCV proportional to mortality from HIV • Natural history more fibrotic in coinfected patients
Impact of HIV on HCV • HIV infection worsens HCV-related liver disease (in pre-HAART era) • ALT levels higher • Fibrosis more severe • Cirrhosis, liver failure, and HCC more common • Death rates higher • Vertical HCV transmission enhanced
Impact of HCV on HIV • Impaired Th1 function in HIV infection affects appropriate immune response to HCV • Conflicting clinical results • More rapid progression to AIDS or death for HCV genotype 1 • Increasing HIV RNA and decreasing CD4 more likely in co-infected pts
AIDS Incidence by HCV Genotype inGreek Hemophiliacs With HCV/HIV 1.0 P=0.002 Conclusion: Genotype 1 is associated with faster progression to AIDS 0.75 Genotype 1Other genotypes Probability ofdeveloping AIDS 0.5 0.25 0 0 4 8 12 16 After HIV seroconversion (yr)
HCV Treatment Rationale • Treatment may improve HCV outcomes • Decrease fibrosis • Increase T-cell responsiveness to HCV antigens • Decrease rate of fatal hepatocellular carcinomas • Treatment may improve HIV outcomes • Reduce hepatic toxicity of ARVs
HCV Treatment Options • Interferon monotherapy • Sustained response rates similar to HCV-infected alone • 8% - 44% • Minimal correlation with CD4 counts • Interferon-ribavirin combination therapy • Trials ongoing • Preliminary findings encouraging
Treatment of HCV in HIV+ Patients 5 MU TIW 3 mo, Responder 3 MU 9 mo n=80 32.5% 22.5% Patients (%) Complete response Sustained response Soriano et al. Clin Infect Dis 1996;23:585
Interferon-Ribavirin Therapy • Cohort study with 37 pts • 84% of patients on HAART with stable HIV disease • Median baseline CD4 343 • Median baseline HIV RNA < 400 c/mL • 59% on combination therapy • 41% on IFN monotherapy
Interferon-Ribavirin Therapy: Interim Results • Analysis of 27 patients at 12 weeks of treatment • 50% of combo arm had undetectable HCV RNA vs 9% on mono arm • No significant change in HIV RNA • Similar results in NYC cohort on HAART • Absolute CD4 count drop (529 to 277) without change in CD4 %
Interferon-Ribavirin Toxicity • Flu-like symptoms • Depression • Leukopenia • Anemia • ? Reduced effectiveness of ARV therapy with ribavirin • May inhibit intracellular AZT and d4T phosphorylation
Conclusions • Natural course of chronic HCV accelerated by concurrent HIV infection • Coinfected patients with stable HIV and good clinical, functional status should be considered for treatment • New treatment options for chronic HCV should be urgently explored
HCV Future Treatment Options • HCV-specific viral enzyme inhibitors • Helicase • Protease • RNA polymerase • Internal ribosomal entry site inhibitors • Antisense nucleotides • Vaccination
Case 1 • 39 y/o HIV-infected man • HIV+ in 5/98 • PCP in 12/98 • Elevated LFTs and HCV antibody + in 12/98 • Began HAART in 1/99 • d4T, 3TC, NVP • Labs • ALT 100-200 u/l (2-4x ULN) • CD4 300 (from 80), HIV RNA <400
Case 1: Antiretroviral Treatment • d4T, 3TC, NVP (transaminitis) • d4T, 3TC, ABC (worsening transaminitis) • ARVs stopped (transaminitis resolved) • d4T, 3TC, NLF (transaminitis)
Case 1:Management Challenge • Stop ARVs and treat HCV • Continue ARVs and treat HCV • Continue ARVs and biopsy liver
Case 2 • 34 y/o HIV-infected man • HIV+ in 1991 • H/O IDU and alcohol use • Persistent transaminitis (ALT 160-280) • Negative HBV and HCV serologies • HCV RNA > 1,000,000 c/mL
Case 2: Diagnosis • Liver biopsy • Fibrous expansion of portal areas, portal inflammation, piecemeal necrosis, activity in >2/3 of lobules
Case 2: HIV Therapy • Initial CD4 50, HIV RNA 100,000 • 6/98 d4T, 3TC, ADF (renal toxicity) • 8/98 ABC, 3TC, NLF, EFV • 11/98 NLF stopped for rash • 12/98 transaminitis • 3/99 all ARVs stopped (despite VL>1 mil) • 6/99 d4T, 3TC, ABC, NLF (jaundice)
Case 2: Management Challenge • Hold ARVs until LFTs normalize, then restart with different agents • Stop ARVs and treat HCV • Continue ARVs and treat HCV
Consultation Services for Clinicians Caring for Patients with HIV/AIDS • Local expert clinicians • Regional and local AIDS Education and Training Centers • National HIV Telephone Consultation Service (Warmline) • (800) 933-3413 • National Clinicians’ Post-Exposure Prophylaxis Hotline (PEPline) • (888) HIV-4911
A Joint Program of UCSF and San Francisco General Hospital Supported by HRSA and CDC http://www.ucsf.edu/hivcntr PEPLine (888) 448-4911 Warmline (800) 933-3413 National HIV/AIDS Clinicians’ Consultation Center