Safety and efficacy of rituximab treatment for vasculitis in hepatitis B virus-associated type II cryoglobulinemia: a case report
© Pasquet et al; licensee BioMed Central Ltd. 2012
Received: 26 September 2011
Accepted: 27 January 2012
Published: 27 January 2012
Systemic B-cell depletion and clinical remission of the systemic effects of cryoglobulins have already been achieved using rituximab in hepatitis C virus-positive immunocompetent patients. Conversely, to the best of our knowledge there are no reports in the literature regarding the use of rituximab in hepatitis B virus-associated cryoglobulinemia.
We report here the case of a 60-year-old Caucasian man who presented with hepatitis B virus-associated type II cryoglobulinemia with severe multisystem disease, including membranoproliferative glomerulonephritis with acute renal failure. The vasculitis was refractory to conventional and antiviral therapy but rituximab use led to a fall in cryoglobulin levels and disease control. The B-cell depletion was safe and efficient to induce a complete remission of the disease.
Our case highlights the benefit and the efficacy of rituximab in association with antiviral therapy in small vessel vasculitis related to hepatitis B virus-associated mixed cryoglobulinemia.
Cryoglobulinemia is a disease characterized by immunoglobulins that are soluble at 37°C, precipitate in the cold, and redissolve when heated. Cryoglobulins may precipitate in the microvasculature and are usually associated with inflammatory manifestations in the vessel walls . Three types of cryoglobulinemia are recognized, according to the cryoprecipitated immunoglobulins. In type I, a monoclonal immunoglobulin is identified. In types II and III, called mixed cryoglobulinemia (MC), two classes of immunoglobulins are present: a polyclonal immunoglobulin G (IgG) and an immunoglobulin M (IgM) with rheumatoid factor activity, the latter either monoclonal in type II or polyclonal in type III. Type II cryoglobulinemia is often associated with hepatitis C virus (HCV) infection  and is less common with hepatitis B virus (HBV) infection. The few historical series of cryoglobulinemia with HBV infection reported in the literature were not able to determine the role of co-infection with HCV [3–5]. The disease expression is variable, ranging from mild clinical symptoms (purpura, arthralgia) to fulminant life-threatening complications (glomerulonephritis, widespread vasculitis). Conventional treatment of MC vasculitis is not yet standardized, but in the absence of viral infection, this treatment typically involves corticosteroids, immunosuppressive drugs and plasma exchange. A recent study has highlighted the efficacy and the steroid-sparing effect of rituximab in non-viral cryoglobulinemia vasculitis, but has also reported the occurrence of severe infections . Treatment of HCV-MC vasculitis may target either the viral trigger (HCV) or the downstream B-cell arm of autoimmunity [7, 8]. Few data are available for the treatment of the HBV-associated cryoglobulinemia . Even if rituximab was shown to be a cause of fatal hepatitis due to B virus reactivation, this drug could be a promising treatment in this kind of vasculitis.
We report here a case of HBV-associated type II cryoglobulinemia with severe multisystem disease, which was refractory to conventional therapy and antiviral agents but in which rituximab led to a fall in cryoglobulin levels and disease control.
A 60-year-old Caucasian male patient with a six-month history of relapsing rash, sicca syndrome, abdominal pain and peripheral edema was admitted to hospital for further investigation. A physical examination showed bilateral edema and hypertension (blood pressure 200/108 mmHg), while a chest X-ray confirmed bilateral pleural effusions and showed an enlarged cardiac silhouette. There was marked (4+) pitting edema of both forearms and legs, extending up to his thighs. A neurologic examination was normal. A cardiac examination revealed a systolic murmur in the left side of his sternum. Raised purpuric lesions were present on his left leg. His right third proximal interphalangeal joint, left elbow and right knee were slightly warm to the touch at examination, without effusion. Our patient described symptoms that suggested the presence of Raynaud's phenomenon.
A diagnosis of MC vasculitis with glomerulonephritis was made and treatment initiated with intravenous methylprednisolone (1 g/day for three days) and oral prednisolone (60 mg daily), thereafter associated with antiviral therapy (lamivudine). One week later, because of gradual deterioration in renal function (serum creatinine 620 μmol/L; urine protein 12 g/24 h) and a falling hemoglobin level (6.9 g/dL), our patient underwent plasma exchange (60 mL/kg/day for 15 days). The subsequent course was complicated by severe sepsis due to Pseudomonas aeruginosa, requiring intensive care and dialysis.
Cyclophosphamide was stopped, antiviral therapy was switched from lamivudine to entecavir and our patient then received a monoclonal anti-CD20 antibody, rituximab, 375 mg/m2, as four-weekly infusions with oral prednisolone (25 mg/day). This led to a depletion of circulating B-cells. His purpura remitted, the proteinuria declined (0.56 g/day) and his renal function returned to normal (creatininemia, 95 μmol/L). His cryocrit and rheumatoid factor fell and complement levels rose. The HBV viral load became undetectable. Mycophenolic acid was begun after the four rituximab infusions as maintenance therapy and our patient was then discharged from hospital. One year after his initial admission, our patient felt well, and took medication including mycophenolic acid, entecavir and irbesartan. The creatininemia level was within normal range at 88 μmol/L and the level of rheumatoid factor remained negative. The HBV viral load remained undetectable.
Cryoglobulinemia is a heterogeneous disease characterized by the appearance of cryoglobulin, which precipitates at low temperature in serum, deposits in microvessels and suggests angiitis, leading to manifestations including skin ulcer, purpura and glomerulonephritis . In chronic viral infection, such as HBV and HCV infection, cryoglobulin consists in heterogeneous antigen-antibody immune complexes containing virus particles, IgG and IgM . In our patient, the initial HBV viral load was probably low because virus particles were trapped in the cryoglobulins, as described in HCV-associated MC. Suppression of viral replication resolves cryoglobulinemia in some cases. For instance, interferon and B-cell depletion therapy for HCV is reported to improve cryoglobulinemia and vasculitis . However, lamivudine given for exacerbated chronic hepatitis B did not improve the cryoglobulinemic vasculitis. On the other hand, rituximab is a chimeric monoclonal antibody that binds to the B-cell surface antigen CD20. It interferes with monoclonal IgM production, cryoglobulin synthesis and renal deposition of immune complexes . Rituximab infusion results in rapid B-cell depletion in the peripheral blood. To the best of our knowledge, there has been no report in the literature on the use of rituximab in HBV presenting with MC. Our case remains very striking because several investigators have reported fulminant hepatitis caused by HBV reactivation  after rituximab therapy. Some researchers have also reported prophylaxis using lamivudine for HBV infection while the patients were also receiving rituximab. Indeed, HBV reactivation during the fourth to sixth (or between the third and fifth) cycles of rituximab treatment was reported, and one study markedly documented late HBV reactivation several months after the completion of rituximab treatment .
As the use of rituximab appears to be a safe and effective therapeutic option in symptomatic patients with HCV-associated MC with signs of systemic vasculitis, we decided to treat our patient with rituximab along with a highly active antiviral therapy such as entecavir.
Rituximab can represent a safe and effective alternative to standard immunosuppression in HBV-associated type II MC, especially with severe manifestations such as diffuse membranoproliferative glomerulonephritis and when the antiviral therapy is not efficient in improving the kidney disease.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
hepatitis B virus
hepatitis C virus
This study had no financial support.
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