Abstract

Snakebites are a relatively rare medical emergency in Europe. In more than half of the annual cases caused by Vipera ammodytes, Vipera berus, and Vipera aspis, immunotherapy with animal-derived antivenom is indicated. Among eight products recently identified as available against European medically relevant species, only Zagreb antivenom, Viperfav, and ViperaTAb have been used almost exclusively for decades. Zagreb antivenom comprises V. ammodytes-specific F(ab′)2 fragments. Viperfav is a polyspecific preparation based on F(ab′)2 fragments against V. aspis, V. berus, and V. ammodytes venoms. ViperaTAb contains Fab fragments against the venom of V. berus. In 2014 the production of Zagreb antivenom was discontinued. Additionally, in the period of 2017 to 2018 a shortage of Viperfav occurred. Due to a lack of the product indicated for the treatment of V. ammodytes bites, other antivenoms were implemented into clinical practice without comparative assessment of their eligibility. The aim of our work was to identify a high-quality antivenom that might ensure the successful treatment of V. ammodytes and V. berus bites at the preclinical level. Differentiation between bites from these two species is difficult and unreliable in clinical practice, so the availability of a unique antivenom applicable in the treatment of envenoming caused by both species would be the most advantageous for Southeastern Europe. Zagreb antivenom, Viperfav, and ViperaTAb, as well as Viper venom antitoxin for V. berus envenoming and the in-development Inoserp Europe, which was designed to treat envenoming caused by all medically important European snakes, were comparatively tested for the first time. Emphasis was placed on their physicochemical properties, primarily purity and aggregate content, as well as their in vivo protective efficacies. As Zagreb antivenom is no longer available on the European market, Viperfav is the highest-quality product currently available and the only antivenom whose neutralisation potency against V. ammodytes and V. berus venoms was above regulatory requirements.

Highlights

  • Snakebites are a relatively rare medical emergency in Europe, but their evolution may sometimes present haematological, cardiovascular, neurological, or local surgical complications [1]

  • According to the systematic review of articles relating to anti-Vipera spp. antivenoms in Europe performed by Lamb et al [2], about 95% of all reported cases were treated with the European viper venom antiserum (Zagreb antivenom, Croatia), Viperfav (France), or ViperaTAb (UK), which differ in several aspects

  • Zagreb antivenom comprises equine V. ammodytes-specific F(ab0 )2 fragments whose paraspecific effectiveness against the venoms of several other medically important European snakes has been demonstrated through continuous use over 40 years in the treatment of envenoming induced by V. aspis (Italy) [4] and V. berus (UK, Sweden) [5,6,7], as well as Macrovipera lebetina and Montivipera xanthina (Turkey) [8]

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Summary

Introduction

Snakebites are a relatively rare medical emergency in Europe, but their evolution may sometimes present haematological, cardiovascular, neurological, or local surgical complications [1]. Zagreb antivenom comprises equine V. ammodytes-specific F(ab0 ) fragments whose paraspecific effectiveness against the venoms of several other medically important European snakes has been demonstrated through continuous use over 40 years in the treatment of envenoming induced by V. aspis (Italy) [4] and V. berus (UK, Sweden) [5,6,7], as well as Macrovipera lebetina and Montivipera xanthina (Turkey) [8]. Viperfav is a polyspecific preparation based on F(ab0 ) fragments of equine origin against V. aspis, V. berus, and V. ammodytes venoms It has been authorised for use in France since 1999 and is considered clinically efficient and safe [9,10,11]. It is indicated solely for the therapy of V. berus snakebites and has proved to be well-suited for envenomation in the UK and Scandinavia [6,7,12,13]

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