key: cord-0880610-1xu5ufn7
authors: Maieron, Andreas; Kerschner, Heidrun
title: Teicoplanin therapy leading to a significant decrease in viral load in a patient with chronic hepatitis C
date: 2012-06-11
journal: J Antimicrob Chemother
DOI: 10.1093/jac/dks217
sha: 775a06e57107353982316ddafd9ce07df74cd827
doc_id: 880610
cord_uid: 1xu5ufn7

nan

We read with interest the paper by Obeid et al., 1 'Inhibition of hepatitis C virus replication by semi-synthetic derivatives of glycopeptide antibiotics'. It provided us with a possible explanation for a clinical observation that we made.

We would like to report an elderly patient with chronic hepatitis C. The patient's alanine aminotransferase levels were consistently 120 U/L and a Fibroscan showed liver stiffness of 43.5 kPa correlating with stage IV fibrosis in 2010. The patient had completed a total of three antiviral treatment cycles with pegylated interferon and weight-based ribavirin. The last course of therapy had been maintained for 72 weeks and was finished in April 2010. Although the patient experienced on-treatment response, relapse occurred very shortly after the end of each therapy.

In April 2010, the patient received a right hip joint replacement in another hospital, which was complicated by delayed wound healing. On 31 May 2010, the patient fell on their hip and had to have repeat surgery. During the following days a fever developed and on 4 June two blood cultures were positive for Staphylococcus aureus. The surgical site was presumed the focus of infection and an antimicrobial therapy with ampicillin/ sulbactam was initiated. The patient was then transferred to the gastroenterology ward of our hospital on 28 June 2010. In consultation with infectious diseases specialists and orthopaedic surgeons, we decided to switch the antimicrobial therapy to long-term teicoplanin starting on 7 July. We administered 1600 mg of teicoplanin intravenously two to three times a week for a total of 10 weeks (trough level 9.2-19.9 mg/L). Surprisingly, 12 days after the initiation of teicoplanin treatment, normal serum transaminase levels were measured for the first time in 30 years. Hepatitis C viral load measurement on 13 August showed a significant decrease in the patient's RNA load to 2.0 log 10 IU/mL (previous measurement on 28 June: 6.9 log 10 IU/mL). Subsequent measurements yielded RNA loads of ,15 IU/mL on 27 August and 2.9 log 10 IU/mL on 17 September, which was the last day of teicoplanin therapy ( Figure 1 ). Transaminase levels remained normal until 1 October, but have been elevated since. Also, the patient's hepatitis C RNA levels returned to the usual baseline levels of 6.0 log 10 IU/mL.

There is some evidence that glycopeptides and their derivatives show antiviral effects against retroviruses and coronaviruses, 2,3 but Obeid et al. 1 were the first to report activity of teicoplanin derivatives against hepatitis C virus replicons in an in vitro model. The mechanism of action of these compounds and the exact molecular substructures responsible for inhibition of viral replication have not yet been elucidated. However, the authors speculate that the peptide scaffold common to all these substances might play a major role in their antiviral activity.

Our patient showed significant decreases in the hepatitis C viral load and transaminase levels during teicoplanin therapy. Teicoplanin has been shown to enter human cells 4 and therefore a post-entry interaction with the hepatitis C virus replication cycle, as proposed by Obeid et al. 1 for their compound LCTA-949, may be a possible explanation for the observed effect. Another conceivable mechanism might be interference of teicoplanin with host cell factors such as lipid metabolism and membrane organization, which are both important for hepatitis C virus replication. 5 It has been suggested that heterologous viral infections may trigger hepatitis C virus-specific T cell responses; 6,7 however, hepatitis B virus and HIV infection were excluded in our patient. Furthermore, our patient did not show any clinical signs of influenza and there was no influenza activity in Austria at that time. In the absence of any other explanation, we speculate that teicoplanin interfered with hepatitis C virus replication and led to the observed decrease in the viral load.

Unfortunately, our patient was not available for a trial of repeat exposure to teicoplanin, because the patient is currently undergoing treatment with triple antiviral therapy. To the best of our knowledge this is the first description of a possible effect of teicoplanin on in vivo hepatitis C virus replication.

This study was carried out as part of our routine work.

None to declare.

Sir, Maraviroc is a chemokine CCR5 coreceptor antagonist that is currently used in treatment-experienced R5-tropic HIV-1-infected patients. Despite the fact that very few data are available on this new antiretroviral drug in HIV-2 infection, in vitro maraviroc activity against R5 HIV-2 has very recently been shown. 1, 2 However, the clinical usefulness of maraviroc in HIV-2 infection 

Inhibition of hepatitis C virus replication by semi-synthetic derivatives of glycopeptide antibiotics

Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics

Polycyclic peptide and glycopeptide antibiotics and their derivatives as inhibitors of HIV entry

Pharmacodynamic evaluation of the intracellular activities of antibiotics against Staphylococcus aureus in a model of THP-1 macrophages

The dependence of viral RNA replication on co-opted host factors

Heterologous immunity between viruses

Cross-reactivity between hepatitis C virus and influenza A virus determinant-specific cytotoxic T cells

Advance Access publication 22

Long-term maraviroc use as salvage therapy in HIV-2 infection

Marinho 2 , Inê s Faustino 2 , Ná dia M. Grilo 2 , Fá tima Lampreia 1 , Isabel Germano 1 , Emília C. Monteiro 2 and Sofia A

Faculdade de Ciências Médicas (FCM)

E-mail: sofia.pereira@fcm.unl.pt Keywords: CCR5 antagonists, HIV-2 CCR5 tropism, therapeutic drug monitoring, second-line HIV-2 therapy