Civacir immune globulin may help prevent HCV reinfection after liver transplant

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Civacir, a hepatitis C immune globulin or antibody product, reduced the likelihood of hepatitis C virus infecting the new liver graft after transplantation in people who were receiving, but had not yet completed, antiviral treatment, according to preliminary study findings presented at the European Association for the Study of the Liver (EASL) 50th International Liver Congress last month in Vienna, Austria.

Without treatment, hepatitis C virus (HCV) almost always infects the donor liver after a transplant, and recurrence is the leading cause of graft loss and liver disease progression. Effective direct-acting antiviral therapy that leads to sustained virological response can prevent reinfection, but people receiving antiviral treatment at the time of transplantation remain at risk.

Norah Terrault of the University of California at San Francisco and colleagues are conducting an ongoing randomised phase 3 study (NCT01804829) to evaluate hepatitis C immune globulin (HCIG or Civacir) for prevention of post-transplant HCV recurrence. Civacir, being developed by Biotest Pharmaceuticals, is a human immune globulin product derived from hundreds of screened blood donors with high HCV antibody levels. Use of multiple donors increases antibody diversity and improves its activity against a variety of HCV strains.



A drug that acts against a virus or viruses.


Proteins found in the blood and cerebrospinal fluid. They carry enzymes, antibodies (immunoglobulins) and other proteins.


In HIV, synonym for superinfection. In hepatitis C, used when someone who has been cured of the virus is infected with hepatitis C again.

detectable viral load

When viral load is detectable, this indicates that HIV is replicating in the body. If the person is taking HIV treatment but their viral load is detectable, the treatment is not working properly. There may still be a risk of HIV transmission to sexual partners.

Child-Pugh score

A classification system used to measure liver function, especially in people with chronic liver disease. The score includes 5 clinical measures of liver disease, including ascites, encephalopathy, serum bilirubin level, serum albumin level, and prothrombin time.

This preliminary analysis, presented as a late-breaking poster, included 63 people with hepatitis C with advanced liver disease on the transplant waiting list, enrolled as of late January 2015. More than 80% were men, most were white and the mean age was 61 years. Most (93%) had HCV genotype 1, with the rest having genotypes 2 or 3. The median MELD score was 19, the median Child-Pugh score was 7 and 77% had hepatocellular carcinoma. People with hepatitis B co-infection and those getting HCV-infected liver grafts were excluded.

Participants could be taking any antiviral regimen that resulted in HCV RNA <100 IU/ml within 4 weeks prior to transplantation. More than 90% received regimens containing sofosbuvir (Sovaldi), including 63% taking sofosbuvir plus ribavirin and 21% taking sofosbuvir plus simeprevir (Olysio); the rest used various interferon-containing regimens.

Treatment had been ongoing for a median of 64 days, or just over 9 weeks, at the time of transplantation; nearly half had not yet received the full typical 12-week course of sofosbuvir and none had received the 24-week course recommended for harder-to-treat patients. Fifteen per cent had detectable HCV viral load at the time of transplantation.

Participants in this open-label study were randomly assigned to receive either 200 or 300mg/kg HCIG or else standard-of-care treatment (antivirals only). Those assigned to HCIG received sixteen infusions around the time of transplantation and immediately thereafter for 10 weeks.

Preliminary results showed that only one out of 21 patients (5%) in the HCIG 300mg/kg arm experienced HCV reinfection after transplantation. Seven out of 22 people (32%) in the HCIG 200mg/kg arm and six out of 20 patients (30%) in the control arm experienced reinfection, indicating that the lower dose performed no better than not using HCIG at all. Five out of nine patients (55%) who had detectable HCV viral load in the 200mg/kg and control arms experienced HCV recurrence.

Anti-HCV antibody titres remained elevated (around 1.5- to 2-fold higher) in the 300mg/kg HCIG arm relative to the 200mg/kg and control arms, indicating ongoing protection over the course of the study.

HCIG was generally safe and well-tolerated, with no drug-related serious adverse events seen to date. Nine people discontinued treatment early, including three due to adverse events. The most frequently reported adverse events were related to underlying liver disease, surgery-associated events and symptoms such as fever known to be associated with use of human immune globulins.

"These preliminary results suggest that Civacir 300mg/kg can increase the proportion of patients on pre-liver transplantation antiviral therapy achieving prevention of HC recurrence post-liver transplantation," the researchers concluded.

They added that this evaluation justified continuing enrolment in the 300mg/kg arm, but not in the 200mg/kg low-dose arm, which has been closed.


Terrault N et al. Novel approach for the prevention of recurrent hepatitis C in liver transplant recipients: preliminary results from ongoing phase III trial with Civacir. EASL 50th International Liver Congress, Vienna, abstract LP17, 2015.