Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/111983
Title: Varicella zoster virus-specific hyperimmunoglobulin in the adjuvant treatment of immunocompromised herpes zoster patients : a case series
Author(s): Terheyden, PatrickLook up in the Integrated Authority File of the German National Library
Sunderkötter, CordLook up in the Integrated Authority File of the German National Library
Söhngen, Franz-DietmarLook up in the Integrated Authority File of the German National Library
Golle, LindaLook up in the Integrated Authority File of the German National Library
Schimo, SonjaLook up in the Integrated Authority File of the German National Library
Baron, RalfLook up in the Integrated Authority File of the German National Library
Maihöfner, Christian GertLook up in the Integrated Authority File of the German National Library
Binder, AndreasLook up in the Integrated Authority File of the German National Library
Pönisch, WolframLook up in the Integrated Authority File of the German National Library
Issue Date: 2023
Type: Article
Language: English
Abstract: Introduction: Immunocompromised patients are at increased risk for herpes zoster (HZ)-associated complications. Despite standard therapy with systemic antiviral drugs and analgesics, complications are frequently encountered, including generalization of lesions or persistent neuropathic pain, so-called post-herpetic neuralgia (PHN). Given the scarcity of literature and awareness of therapeutic options to improve patient outcomes, especially for vulnerable patient groups, here we describe a strategy based on early intensification of treatment with a varicella zoster virus-specific hyperimmunoglobulin (VZV-IgG), which is approved in the adjuvant treatment of HZ. Methods: For this case series, we selected four cases of HZ in patients with impaired immunity due to hemato-oncologic disease or immunosuppressive treatment who presented with either existing generalized lesions and/or severe pain or with other risk factors for a complicated HZ course such as PHN. They were considered to be representative examples of different patient profiles eligible for intensification of treatment by the addition of VZV-IgG to virostatic therapy. Case Report: All patients showed a rapid response to combined treatment with VZV-IgG and a virostatic agent. In two patients who had generalized lesions, the formation of new lesions ceased 1 day after VZV-IgG infusion. One patient, with mantle cell lymphoma, achieved complete healing of the lesions 9 days after diagnosis of HZ, a rare occurrence compared to similar cases or cohorts. A patient with HZ in the cervical region showed a good response after a single dose of VZV-IgG. None of the patients developed post-zoster-related complications. Combination therapy of a virostatic agent and VZV-IgG was well tolerated in these four cases. Conclusion: This case series demonstrates highly satisfactory treatment effectiveness and tolerability for VZV-IgG in the adjuvant treatment of immunocompromised HZ patients and supports early intensification of HZ therapy in patients at high risk of severe disease progression.
URI: https://opendata.uni-halle.de//handle/1981185920/113941
http://dx.doi.org/10.25673/111983
Open Access: Open access publication
License: (CC BY-NC 4.0) Creative Commons Attribution NonCommercial 4.0(CC BY-NC 4.0) Creative Commons Attribution NonCommercial 4.0
Journal Title: Dermatology and therapy
Publisher: Springer
Publisher Place: Heidelberg
Volume: 13
Original Publication: 10.1007/s13555-023-01019-6
Page Start: 2461
Page End: 2471
Appears in Collections:Open Access Publikationen der MLU

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