Title: Hepatitis and HIV CoInfection
1Hepatitis and HIV Co-Infection
- Sandra G. Gompf, MD, FACP, FIDSA
- Associate Professor, Infectious Diseases and
International Medicine - University of South Florida College of Medicine
2Disclosure of Financial Relationships
- This speaker has no significant financial
relationships with commercial entities to
disclose.
This slide set has been peer-reviewed to ensure
that there areno conflicts of interest
represented in the presentation.
3The Big Picture of Hepatitis
- Damage to liver cells caused by inflammation or
cell death - Can be caused by infections, drug toxicity,
poisoning, biliary tract obstruction - If persists, can lead to progressive scarring of
the liver (cirrhosis) and end-stage liver
dysfunction
4Causes of Hepatitis in the HIV Patient
- Drugs
- HAART
- Metabolic complications
- Treatment of opportunistic infection
- Viral pathogens
- Hepatitis A, B, C
- CMV
- Overlap is common
5Drug-Induced Hepatotoxicity, Besides HAART
- trimethoprim-sulfamethoxazole, antituberculars,
azole antifungals - anabolic steroids
- acetaminophen
- statins fibrates
6HAART-Associated Hepatotoxicity
- Elevated transaminases mostly with PIs, but also
w/ NNRTIs - Probably hyperimmunity or immune restoration
syndrome - Often subsides over several months
- HIV/HCV 3-5-fold more likely to develop severe
transaminitis
7HAART-Associated Immune Restoration
- Ofotokun et al. Am J Med Sci 11/07, HAART-naïve
pts - Elevated liver enzymes were associated with HBV
or HCV co-infection, stavudine - Robust rise in CD4 count/month associated with
co-infection abnormal LFTs - HIV/HCV or HBV abnormal LFTs 99/mm3
- HIV/HCV or HBV normal LFTs 62/mm3
- HIV normal LFTs 59/mm3
- HIV abnormal LFTs 36/mm3
8Viral Hepatitis in HIV Patients
- Acute viral hepatitis may be severe or fatal
- Acute viral hepatitis may add to liver damage
already present from other causes - e.g. Acute hepatitis A on chronic hepatitis C may
be deadly
9Viral Hepatitis Overview
10GBV-C Infection the Role ofHepatitis G
- may reduce mortality in late HIV
- may reduce HIV viral loads
W Zhang, et al. Effect of Early and Late GB Virus
C (GBV-C) on the Survival of HIV-infected
Individuals a Meta-analysis. HIV Med 7(3)
173-180. April 2006. KS Howard, et al. No
observed effect of GB virus C coinfection on
disease progression in a cohort of African woman
infected with HIV-1 or HIV-2. Clin Infect Dis
40(6)876-8. February 2005. H L Tillmann, et al.
Infection with GB Virus C and Reduced Mortality
among HIV-Infected Patients N Engl J Med 345(10)
715 - 724. September 2001. JXiang S et al.
Effect of Coinfection with GB Virus C on Survival
among Patients with HIV Infection N Engl J Med
345(10) 707 - 714. September 2001.
11Hepatitis A HIV, in Brief
- role seems significant
- 35 HIV with acute HAV
- 80 treatment interrupted X 2 months
- 25 lost efficacy on resuming HAART
- safe, effective VACCINE available
Berggren RE et al. 39th ICAAC, 9/26-29/99, San
Francisco, CA. Abstract 97.
12Hepatitis C
- Transmitted via IVDU/blood, less often sex (more
likely for MSM) - In U.S., 4 million HCV ? 85 chronic
- If chronic ? 20 cirrhotic _at_ 20 years
- Once cirrhotic ? 25 hepatocellular CA
- (0.5 of total HCV)
- Alcohol HIV worsen prognosis
- Usually no symptoms
- sometimes fatigue, RUQ ache, difficulty
concentrating
13Hepatitis C
- 6 Genotypes
- Genotypes 1-3 are commonest in US, WEurope
- 75 are 1
- 25 are Non-1
- Most are 2 3
- 4-6 Middle East/Africa/?Spain
- African Americans less likely to achieve
sustained virologic response (SVR) to treatment - 28 AA
- 52 Cauc
H S Conjeevaram, M W Fried, L J Jeffers, et al.
Gastroenterology. 131(2) 470-477. August
2006. SM Martinez, et al. Clin Microbiol. 43(10)
54035404 October 2005.
14Hepatitis C
- Like HIV, antigenic variation occurs
- ? Hepatitis C antibody is not protective
- ? no vaccine
- Unlike HIV HBV, does not integrate into the
host genome - ? eradication is possible / more likely with
treatment
15Sources of Infection for Persons with Hepatitis C
- 30-50 HIV have chronic HCV
- HIV/HCV
- IVDU 90
- hemophilia 80
- MSM 4-8
CDC
16HIV/HCV Co-Infection is Clearly Associated with
More Rapid Progression to Cirrhosis
- Soto, et al. J Hepat 1997
- compared 547 HIV- with 116 HIV
- all with chronic hepatitis C
- Incidence of cirrhosis
- HIV-
- 2.6 (mean HCV duration 23.2 years)
- HIV
- 14.9 (mean HCV duration 6.9 years)
17Other Possible Interactions between Hepatitis C
HIV
- HCV does not appear to consistently affect
progression of HIV disease - chronic HCV does not appear to consistently
affect CD4 response to HAART - cirrhosis suppresses immunitymay affect CD4
N Soriano-Sarabia, A Vallejo, S Molina-Pinelo.
AIDS 21(2) 253-255. January 11, 2007. B H
McGovern, Y Golan, M Lopez, et al. Clinical
Infectious Diseases 44(3) 431-437. February 1,
2007. Daar ES, et al. 7th Conference on
Retroviruses and Opportunistic Infections,
1/30-2/2/00, San Francisco, CA. Abstract 280.
18Diagnosing HCV in HIV
- Do not rely on transaminases! There is no
correlation between transaminase levels and
disease severity. - HCV ELISA antibody screening
- Antibody means infected at some point, need to
determine if active or chronic infection - in advanced HIV, may be falsely negative
- HCV RNA PCR confirms or excludes active disease
- Viral load means active hepatitis
19Diagnosing HCV in HIV
- HCV ELISA antibody (low-threshold, sensitive)
- If (or advanced HIV)? HCV RNA quantitative PCR.
- If HCV ELISA or RNA PCR -, no further
intervention. - If HCV RNA PCR ? active hepatitis is present
20Doc, so I have chronic hepatitis, now what?
- STOP ALL ETHANOL
- Genotyping is helpful in predicting response to
therapy - 1 ( 4) is more refractory to treatment
- 2 3 are very responsive
- Rule out other causes of liver disease if liver
enzymes are abnormal - Autoimmune hepatitis, biliary disease,
hemochromatosis
21Look for Complications of Chronic Hepatitis
- Liver biopsy? Gold standard in evaluating
hepatitis and cirrhosishow close to cirrhosis
is your patient? - Fibrosure Fibroscan not validated in HIV yet,
but non-invasive measures of fibrosis - Cannot rule concurrent diseases, over-diagnoses
fibrosis - Fibrosure may be affected by elevated bilirubin
due to atazanavir or indinavir - Sonogram screen for other liver disease, CA
- Alpha-fetoprotein alone is not enough to screen
out CA
22Look for Complications of Chronic Hepatitis
- Extra-hepatic manifestations of Hepatitis C
- Mixed cryoglobulinemia (rash, joint pain)
- Membranous glomerulonephritis (proteinuria)
- These may be reasons to treat BUT
- extrahepatic manifestations may differ in HIV-HCV
- may or may not improve
23Talking to Your Patient Benefits Goals of
Treating Chronic Hepatitis C
- Viral eradication (sustained viral remission,
SVR) - Delay progression of fibrosis
- Prevent/delay bad clinical outcomes of cirrhosis
- Liver decompensation
- Hepatocellular carcinoma
- Death
- Improve tolerance and effectiveness of HAART
- Allows aggressive antiretroviral drug therapy
- Enhanced immune reconstitution?
- Increases survival
24Note BeneWhich Hepatitis Drugs are Which??
- aINF 2b, PEG aINF 2b
- Schering-Plough
- Intron A, PEG-Intron A
- ribavirin (Rebetol)
- aINF 2a, PEG aINF 2a
- Roche
- Roferon-A, Pegasys
- ribavirin (Copegus)
- lamivudine
- Epivir-HBV, 50mg
- Epivir, 150mg (HIV)
- Adefovir
- Hepsera
- Entecavir, Baraclude
- Telbivudine, Tyzeka
Approved by European Union for use in
co-infected patients in 2007
25Talking to Your Patient Benefits Goals of
Treating Chronic Hepatitis C
- In studies, sustained viral remission w/ newer
treatments PEG ?IFN ribavirin - Genotype 1 4 ( 30 -70 SVR)
- Genotype 2 3 (gt80 SVR)
- SVR with PEG ?IFN ribavirin reduces cirrhosis,
HCCA, transplant, death by 9-fold - HIV disease is not affected by ?IFN or ribavirin
L Martin-Carbonero, et al. CROI 2008. Abstract
1052.
26Talking to Your Patient Risks, Problems,
Adverse Effects of Treating Chronic Hepatitis C
in HIV
- Theres still more to talk about..
27Hepatitis C Treatment Toxicities
- Pegylated aINF 2a or 2b
- flu-like symptoms
- depression/suicidal
- fatigue, dizziness
- anorexia, nausea/diarrhea
- bone marrow suppression
- serious infections
- autoimmune disease
- thyroid, diabetes
- hair loss, oral ulcers
- pulmonary fibrosis
- Stevens-Johnson, hypersensitivity
- Ribavirin
- anemia/hemolysis
- dose dependent
- 2.5-3g ? within 4 weeks
- erythopoietin
- bone marrow depression
- embryocidal / Category X
- teratogenic for up to 6 months after treatment
- FDA Ribavirin Pregnancy Registry
28Talking to Your Patient Whom NOT to Treat
- Major contraindications
- pregnant or planning
- untreated/severe depression or psych disease
- significant ischemic cardiovascular disease
- decompensated cirrhosis before/during treatment
- hemoglobinopathies (thalassemia/sickle cell)
- significant asthma, lung disease
- malignancy
- end-stage renal disease
29Talking to Your Patient Whom to Delay or
Re-Consider Treating
- Relative contraindications
- untreated depression or psych disease
- street drug or ethanol abuse
- uncontrolled diabetes or thyroid disease
- seizure disorders
- infections
- poor ADHERENCE (predicts poor adherence to
treatment, BIRTH CONTROL, follow-up visits)
30 HIV Infected Veterans with Co-morbid
Conditions, 2006 (22,638 Total)
Data from VHA HIV Clinical Case Registry
31Talking to Your Patient Best Odds and Best
Reasons to Treat
- Stable HIV disease with intact immune function
- (to eradicate virus, delay cirrhosis/CA)
- Advanced hepatic fibrosis
- (to delay cirrhosis/CA)
- Starting HAART
- (to limit HAART interruptions by hepatotoxicity )
Sulkowski MS, 8th Conf on Retrov and OI, 2000,
Abstract S11
32Talking with Your Patient Which to Treat First?
HIV or HCV?
- CD4 lt 350 ? treat HIV
- Higher risk of HIV morbidity/mortality
- CD4 gt 350 ? treat HCV
- HCV response is better _at_ higher CD4s
- lower pressure to start HAART
- possibly avoid HAART interruptions due to
hepatotoxicity
33Talking to Your Patient Other Issues
- ex-IVDU needle-aversions, needle-fixations
McBride, A.J., Pates, R.M., Arnold, K. and Ball,
N. (2001), Needle fixation, the drug users
perspective a qualitative study, Addiction, 96,
(7) pp 1051 -1060.
34Ribavirin Interacts with HAART
- Didanosine (DDI) should be replaced before
treatment - Ribavirin will markedly increase DDI
- Increased lactic acidosis, mitochondrial
toxicity, peripheral neuropathy pancreatitis - Zidovudine, stavudine therapy should be monitored
for failure, toxicity - RBV inhibits phosphorylation of pyrimidine
nucleoside analogs and raises ZDV levels - Bone marrow inhibition by ZDV RBV may be
additive
35Other HAART Considerations with Hepatitis C
- NNRTIs (efavirenz, nevirapine)
- Increased severe hepatotoxicity is 1 w/ NNRTIs
- NNRTIs need not be withheld in HCV/HIV
- Tenofovir vs. ZDV or abacavir (?)
- Better HCV treatment responses with tenofovir?
- Confounders lower RBV doses
- Sulkowski, et al, 8th COROI, 618 Dieterich et
al, 2002 - JJ Gonzalez-Garcia, et al. GESIDA 05/06 Study
Group. CROI 2008. Abstract 1076 - J Mira, et al. CROI 2008. Abstract 1074.
36Treatment of HCV
- PEG aINF 2a (fixed 180 mcg) or 2b (wgt-based)
subcutaneously every week X 48 weeks -
- Ribavirin 800mg PO daily (1000-1200mg preferable
for genotype 1 or 4) X 48 weeks - If HCV undetectable _at_ 12 weeks (EVR)? continue
- If HCV undetectable _at_ end of tx (ETR)? repeat _at_
72 weeks - if still undetectable ?SVR!!
Off-label in HIV/HCV. Wgt-based regimens may be
more effective in morbidly obese patients.
37Prescreening and Monitoring During Treatment
- Monitoring
- Monthly
- CBC diff ( (_at_ 2 weeks of start)
- lytes, FBS, creatinine, liver enzymes
- serum or urine ß HCG
- _at_ 12, 48, 72 weeks
- HCV RNA PCR
- Every 12 weeks
- serum TSH
- Prescreening tests
- serum or urine ß HCG
- serum TSH
- serum ANA
- iron, ferritin
- HAV HBV serology
- CBC differential
- PT, PTT
- fasting blood glucose, lytes, creatinine, liver
enzymes
38Managing Adverse Effects
- Avoid dose reductions where feasible
- Moderate depression reduce PEG STOP if severe
or suicidal - Neutropenia thrombocytopenia
- G-CSF 300 mcg SC TIW to keep ANC gt 750
- ANC lt 750 reduce PEG
- ANC gt 750 hold PEG, resume at lower dose once
over 750 - PLT lt 50K reduce PEG at lt 25K, D/C PEG
- Anemia
- Reduce RBV if Hgb lt10 mg/dL, D/C if lt 8 mg/dL
- ?Erythropoietin alfa 40K IU SC weekly if Hgb lt12
mg/dL - Risks of tumor growth, vascular disease, etc?
39The Future of HIV/HCV?
- Longer courses of pegylated INF ribavirin
- 72 weeks (indefinite maintenance found of ?
benefit in HIV/HCV who relapse) - maximize ribavirin dose
- Non-invasive fibrosis markers?
- eltrombopag for thrombocytopenia?
- HCV protease polymerase inhibitors?
- Liver transplantation?...
M Nunez, J Garcia-Samaniego, M Romero, and
others. Abstract 365. The PRESCO trial. AASLD.
October, 2006. H Al-Mohri, T Murphy, Y Lu, and
others. JAIDS. January 4, 2007 K Sherman, and
others. CROI 2008. Abstract 59.
40What happens after ESLD?
- Liver transplantation may be a viable option in
selected HIV individuals - Experimental, outcomes similar to HIV-/HCV
- need good HIV control, adherence
- HCV recurrence is common in new liver
- re-treatment x 3 months after transplant
- 5-year survival is 51 (vs.81 in HIV-/HCV)
L Castells, J I Esteban, I Bilbao, and others.
Antiviral Therapy 11(8) 1061-1070. 2006.
41Key Points about HCV/HIV
- HCV is worse in HIV/HCV
- Treat based on individual benefits vs. risks
- If you or patient in doubt, hold off
- Patient must be committed to birth control
- Be aware of HAART interactions
- Be alert to toxicities revisit contraception!
- PEG aIFN ribavirin x 48 weeks is standard
- Vaccinate all co-infected patients against HAV
and HBV if seronegative
42Viral Hepatitis Overview
43Hepatitis B
- Hepatitis B
- sex, perinatal, IVDU, blood
- gt300,000/year in U.S.
- Only 25 symptomatic acute jaundice, elevated
liver enzymes, fatigue, NVD - Lifetime risk up to 100 if risks (avg U.S. 5)
- 10 become chronic ? cirrhosis/CA in 20-30 yrs
- Ethanol, HIV, other hepatitis viruses
44Serology of Chronic HBV
- HBsAg HBsAb HBeAg HBV DNA
- - /-
- Pre-core protein/core promoter mutation
- dont express HBeAg, DNA ??
- severe inflammation?cirrhosis
- longer duration of disease?older
- more resistant to therapy
- non-A genotypes, Asia/Europe
45Serology in Chronic HBV, cont.
- YMDD mutation lamivudine resistance
- 1000x rise in resistance
- Up to 90 resistance _at_ 4 years lamivudine
- Mutations in RT region of HBV DNA pol
- YMDD motif tyrosine, methionine, aspartic acid,
aspartic acid - 2 forms M ? valine or M ? isoleucine
46Hepatitis B HIV
- acute HBV may be more severe
- 10 of HIV
- 5-6x gt chronicity than HBV alone
- impaired cell-mediated immunity can cause chronic
HBV - HIV/HBV 19x gt liver deaths than HBV alone
- 8x gt liver deaths than HIV
alone
Thio C, Seaburg E, Skolasky Jr. R, et al.
Multicenter Cohort Study MACS. Lancet
20023601921-26.
47Hepatitis B HIV
- 7 genotypes (data evolving)
- A commonest in HIV/HBV in U.S. 75
- may respond best
- G least common 25
- marker of rapid fibrosis
- efavirenz exposure
- duration of HIV
K Lacombe and others. AIDS 20(3) 419-427,
February 14, 2006.
48Hepatitis B HIV Occult HBV
- Isolated HBcAb and DNA low level
- HBsAg HBsAb HBcAg HBV DNA
- - - -
- commoner in HIV
Gandhi RT, Wurcel A, Lee H, et al. J Infect Dis
20051911435-41.
49Hepatitis B HIV Occult HBV
- may account for acute hepatitis in
- HAART initiation/immune reconstitution
- Immune suppression (CD4? or chemo-tx)
- probably need HBV vaccine
- Poor anamnestic response, HBcAb
- commonest in HIV/HCV/HBV
Gandhi RT, Wurcel A, Lee H, et al. J Infect Dis
20051911435-41.
50Therapies for Chronic HBV in HIV
- First line
- lamivudine (Epivir)NOT Epivir-HBV
- emtricitabine (Emtriva, off-label for HBV)
- inhibit HBV DNA pol
- YMDD resistance with lamivudine
- 15 _at_ 1 yr
- 30-40 _at_ 2 yr
- 70-90 _at_ 4 yrs
- emtricitabine is equivalent, delayed
resistance/may overcome YMDD
HEP DART 2003. December 14-18, 2003. Kauai,
Hawaii.
51Therapies for Chronic HBV in HIV
- Unlike HAART, combination therapy is no better
than sequential monotherapy in HBV - lamivudine tenofovir/lamivudine
- sequencing or combo depends on HIV HAART
S Maus and others. Abstract 964. American
Association for the Study of Liver Diseases.
November, 2005.
52Therapies for Chronic HBV in HIV
- Second line interferon
- aINF 2b x 48 wk
- 30 SVR (Schering)
- PEG aINF 2a x 48 wk
- 30 SVR
- Roche, 1st PEG FDA approved for HIV/HBV, 2005
- Schering PEG aINF 2b used off-label, more data
for HIV/HCV but not HIV/HBV
53Therapies for Chronic HBV in HIVOther Agents?
- adefovir (Hepsera) NO
- dosing for HBV is too low to suppress HIV
- promotes tenofovir resistance
- entecavir (Baraclude)with CAUTION
- may be associated with M184V resistance mutation,
use only with effective HAART - severe hepatomegaly, lactic acidosis
54Therapies for Chronic HBV in HIVOther Agents?
- telbivudine (Tyzeka)maybe?
- nucleoside analog
- more effective than lamivudine, adefovir
- may have additive benefit with other
agentscombination therapy? - no HIV-1 activity, no apparent NRTI antagonism in
vitro, but no data in HIV - Canadian govt warning peripheral neuropathy
with INFs
55When to Treat with What
- Ready for HAART?
- lamivudine emtricitabine/tenofovir backbones
- indefinite tx
- FLARES with stopping meds or onset of YMDD
resistance USE CAUTION
- Not ready for HAART?
- Consider PEG aINF 2a ribavirin x 48 weeks
- advanced fibrosis
- HIV/HBV/HCV
- improves fibrosis
- may clear virus
- Consider earlier HAART w/ HBV-active agent
(telbivudine?)
56Treatment Options for Lamivudine-Resistant HBV
(YMDD Mutants)
- emtricitabine may still work in YMDD
- tenofovir (off-label for HBV)
- entecavir with caution?
- telbivudine?
- consider PEG aINF 2a ribavirin
- expectant management
57Last words about Hepatitis A, B, C HIV
- Liver transplantation may be a viable option in
selected HIV individuals - Experimental, outcomes similar to HIV-/HCV
- need good HIV control, adherence
- HCV recurrence is common in new liver
- re-treatment x 3 months after transplant
- 5-year survival is 51 (vs.81 in HIV-/HCV)
L Castells, J I Esteban, I Bilbao, and others.
Antiviral Therapy 11(8) 1061-1070. 2006.
58Last words Hepatitis A, B, C HIV
- Prevention is KEY
- Screen vaccinate early
- Lower CD4s will lower antibody response
- CD4 lt 200 15-40 antibody
- CD4 gt500 90 antibody
- ?Re-vaccinate w/ double-dose (50.7 response in
previous non-responders in Dutch prospective
open-label study) - Counsel about risk factors
TE De Vries-Sluijs, et al. JID 197(2) 292-94.
January 2008.
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