Safety of TNF-blocking agents in rheumatic patients with serology suggesting past hepatitis B state: results from a cohort of 21 patients

被引:85
作者
Charpin, Caroline [1 ]
Guis, Sandrine [1 ]
Colson, Philippe [2 ,3 ]
Borentain, Patrick [4 ]
Mattei, Jean-Pierre [1 ]
Alcaraz, Patrice [1 ]
Balandraud, Nathalie [1 ]
Thomachot, Benoit [1 ]
Roudier, Jean [1 ]
Gerolami, Rene [4 ]
机构
[1] Ctr Hosp Univ Concept, Serv Rhumatol, F-13385 Marseille, France
[2] CHU Timone, Fed Hosp Microbiol Clin, Virol Lab, F-13385 Marseille, France
[3] Univ Aix Marseille 2, Fac Med & Pharm, CNRS, URMITE,IRD,UMR 6236, F-13385 Marseille, France
[4] Ctr Hosp Univ Concept, Serv Hepatogastroenterol, F-13385 Marseille, France
关键词
VIRAL-HEPATITIS; CROHNS-DISEASE; ALPHA BLOCKADE; REACTIVATION; INFLIXIMAB; ANTIGEN; THERAPY; NEED;
D O I
10.1186/ar2868
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Reactivation of hepatitis B virus (HBV) infection in patients with past infection has been described in 5% to 10% of individuals undergoing immunosuppressive therapies. No data are available to date on the outcome of patients treated by tumour necrosis factor-alpha (TNF alpha) inhibitors for chronic arthritis with a serological pattern of past HBV infection. The aim of our study was to monitor HBV markers in HBV surface antigen (HBsAg)-negative/anti-HBcAb-positive patients treated with a TNF alpha inhibitor for inflammatory arthritides. Methods Twenty-one HBsAg-negative/anti-HBcAb-positive patients were included. HBV serological patterns were compared with those determined before starting TNF alpha inhibitors. Serum HBV DNA testing by polymerase chain reaction was additionally performed. Spearman correlation analysis was used and P < 0.05 was chosen as the significance threshold. Results Before starting therapy, mean anti-HBsAb titre was 725 IU/L, no patient had an anti-HBsAb titre <10 IU/L, and 18 patients had an anti-HBsAb >100 IU/L. At a mean time of 27.2 months following therapy introduction, mean anti-HBsAb titre was 675 IU/L and anti-HBsAb titre remained >100 IU/L in 17 patients. There was a strong correlation between the first and second anti-HBsAb titres (r = 0.98, P = 0.013). Moreover, no patient had an anti-HBsAb titre below 10 IU/L or HBV reactivation (HBsAg seroreversion or positive HBV DNA detection). However, the anti-HBsAb titre decreased by more than 30% in 6 patients. The mean anti-HBsAb titre at baseline was significantly lower (P = 0.006) and the mean duration of anti-TNF alpha therapy, although non-significant (P = 0.09), was longer in these six patients as compared to patients without a decrease in anti-HBsAb titre. Conclusions Anti-TNF alpha treatments are likely to be safe in patients with past hepatitis B serological pattern. However, the significant decrease of anti-HBsAb titre observed in a proportion of patients deserves HBV virological follow-up in these patients, especially in those with a low anti-HBsAb titre at baseline.
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