- Short report
- Open Access
Clinical significance of 4 patients with chronic hepatitis B achieving HBsAg clearance by treated with pegylated interferon alpha-2a for less than 1 year: a short report
© Yang and Zhao; licensee BioMed Central Ltd. 2009
Received: 24 April 2009
Accepted: 08 July 2009
Published: 08 July 2009
We report 4 chinese patients with hepatitis B e antigen-positive chronic hepatitis B achieving clearance of HBsAg by using pegylated interferon alpha-2a for less than 1 year, to provide one clinical clue for the treatment of chronic hepatitis B.
Chronic infection with Hepatitis B virus(HBV) is a major global health problem, affecting 350–400 million people worldwide [1, 2]. Patients who have HBV infection with positivity for hepatitis B e antigen(HBeAg) and persistently active disease have increased risks for progressive disease leading to liver cirrhosis and hepatocellular carcinoma. Therefore, for patients with HBeAg positive chronic hepatitis B(CHB), anti-viral therapy is most important if they have indications for treatment. The end points to assess efficacy of therapy include: reduction of serum HBV DNA to the undetectable level, normalization of alanine aminotransferase(ALT) levels, HBeAg seroconversion and an improvement of liver disease at histology. But it is gradually thought that the ultimate therapeutic goal of anti-HBV therapy should furthermore make patients achieve clearance of hepatitis B surface antigen(HBsAg) or even HBsAg seroconversion [5, 6]. In view of current anti-HBV drugs, however, it is extremely difficult to implement this goal. Nevertheless, on condition that there is a treatment with effective anti-viral drugs and appropriate therapeutic schemes, some patients may still be able to achieve it.
All 4 patients aged from 14 to 49 yrs-old, including 3 males and 1 female, had suffered from CHB for 1 to 3 years with the sera profile of HBeAg, HBsAg positive, and HBV DNA leveled from 2.71 × 106 copies/mL to 5.00 × 107 copies/mL. They came to our hospital for pegylated interferon alpha-2a(Pegasys) treatment from March 2006 to Ten 2007. All of them had neither complications nor other accompanying diseases, also with no history of anti-HBV drug use.
Methods of treatment
Classification of methods
Pegasys monotherapy Case 1 was treated with pegasys at a dose of 135 ug intracutaneously one time per week(for her age was below 18). Case 2 was treated with pegasys at a dose of 180 ug intracutaneously one time per week.
Sequential therapy As both leucopenia and thrombocytopenia occurred in case 3 and case 4 during the treatment of pegasys, we adopted sequential therapy with pegasys and entecavir(Baraclude). Pegasys was administered at a dose of 180 ug intracutaneously one time per week. Baraclude was administered at a dose of 0.5 mg orally one time per day.
Periodic monitoring of anti-viral therapy
Leukocyte and platelet counts, serum HBV DNA and ALT were detected once every month. HBV markers(HBsAg and anti-HBs, HBeAg and anti-HBe, anti-HBc) were detected once every three months. Among them, serum HBV DNA was arrayed by fluorescent quantitative PCR and HBV markers were arrayed by ELISA.
Therapeutic efficacy of pegasys in 4 patients with chronic hepatitis B
Course of diseasea(yr)
Course of treatmentb(wk)
HBV DNA undetectablec
During the course of pegasys treatment, apparent reduction of leukocyte and platelet counts had occurred in 2 patients (case 3 and case 4) at week 4 and week 10 of therapy respectively, but returned to baseline levels one month after sequential therapy was adopted (pegasys was paused temporarily, baraclude was administered until the leukocyte and platelet counts recovered). There were no other remarkable adverse events in all the four cases during the total course of anti-viral therapy.
The aims of treatment for CHB are to achieve sustained suppression of HBV replication, thereby inducing remission of liver diseases and interrupting progression to liver cirrhosis or hepatocellular carcinoma. Pegylated interferon alpha-2a is created by attaching a large, branched, 40-kD polyethylene glycol molecule to interferon alfa-2a, This allows for convenient once-weekly dosing, with effective serum levels maintained throughout the dosing interval. It could efficaciously inhibit the replication of HBV and help eradicate HBV infectious hepatocytes by dual anti-viral and immunomodulatory mode of action. In contrast to nucleoside analogues, pegylated interferon alpha-2a has a higher rate of HBeAg seroconversion, lower rate of relapse after treatment cessation, moreover, it has not been observed to induce mutation of HBV [11, 12]. However, it has a few adverse events such as transient flu-like symptoms, depression and abnormal blood counts [13, 14]. In this study, both leucopenia and thrombocytopenia had been observed in case 3 and case 4, so we adopted sequential therapy with pegasys and baraclude (one kind of nucleoside analogues). The results showed that their leukocyte and platelet counts gradually returned to the baseline levels one month after pegasys was paused and baraclude was administered sequentially, then we continued the administration of pegasys. For the reason that sequential therapy could effectively evade the inherent adverse events of pegasys and meanwhile, nucleoside analogues could keep sustained suppression of HBV during the time when pegasys is paused, so the advantageous efficacy of pegasys could be brought into play as much as possible.
By analyzing above materials, we had observed one phenomenon that the clearance of HBsAg occurred in the 4 patients not very long(1 wk, 18 wks, 1 wk and 6 wks, respectively) after they had achieved HBeAg seroconversion. This may imply that pegylated interferon alpha-2a probably plays an important role in helping clear HBsAg by means of activating the host immune reaction. Additionally, ALT levels in the 4 patients were elevated during treatment but gradually normalized at the end of therapy, they also had no clinical symptoms. Considering that pegylated interferon alpha-2a takes effect by improving the host immune function, we suppose the occurrence of transient elevated ALT might be a reflection of the course during which HBV infectious hepatocytes are being eradicated.
Although limited case numbers are reported in this article and more patients need to be included for further study, one certain clue, which can be provided to clinical doctors, is that some patients with HBeAg-positive CHB could probably be expected to achieve the ideal therapeutic goal of HBeAg seroconversion, HBsAg clearance and even HBsAg seroconversion if they are treated with effective anti-viral drugs and appropriate therapeutic schemes.
Based on our clinical observation, either pegasys monotherapy or sequential therapy with pegasys and baraclude is efficacious and relatively safe for treating patients with CHB.
We are grateful to Ping Feng for her helpful comments and suggestions.
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