Prevention of Jarisch–Herxheimer Reactions by Treatment with Antibodies against Tumor Necrosis Factor α

  • Fekade D
  • Knox K
  • Hussein K
  • et al.
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Abstract

Background: In patients with louse-borne relapsing fever (Borrelia recurrentis infection), antimicrobial treatment is often followed by sudden fever, rigors, and persistent hypotension (Jarisch-Herxheimer reactions) that are associated with increases in plasma concentrations of tumor necrosis factor α (TNF-α), interleukin-6, and interleukin-8. We attempted to determine whether sheep polyclonal Fab antibody fragments against TNF-α (anti-TNF-α Fab) could suppress the Jarisch-Herxheimer reaction. Methods: We conducted a randomized, double-blind, placebo-controlled trial in 49 patients with proven louse-borne relapsing fever. Immediately before the intramuscular injection of penicillin, the patients received an intravenous infusion of either anti-TNF-α Fab or a control solution. Results: Ten of the 20 patients given anti-TNF-α Fab had Jarisch-Herxheimer reactions with rigors, as compared with 26 of the 29 control patients (P=0.006). The controls had significantly greater mean maximal increases in temperature (1.5 vs. 0.8°C, P<0.001), pulse rate (31 vs. 13 per minute, P<0.001), and systolic blood pressure (25 vs. 15 mm Hg, P<0.003), as well as higher mean peak plasma concentrations of interleukin-6 (50 vs. 17 μg per liter) and interleukin 8 (2000 vs. 205 ng per liter) (P<0.001 for both comparisons). Levels of TNF-α were undetectable after treatment with anti-TNF-α Fab. Conclusions: Pretreatment with sheep anti-TNF-α Fab suppresses Jarisch-Herxheimer reactions that occur after penicillin treatment for louse-borne relapsing fever, reduces the associated increases in plasma concentrations of interleukin-6 and interleukin-8, and may be useful in other forms of sepsis.

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APA

Fekade, D., Knox, K., Hussein, K., Melka, A., Lalloo, D. G., Coxon, R. E., & Warrell, D. A. (1996). Prevention of Jarisch–Herxheimer Reactions by Treatment with Antibodies against Tumor Necrosis Factor α. New England Journal of Medicine, 335(5), 311–315. https://doi.org/10.1056/nejm199608013350503

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