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Updated: Jun 24, 2025

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Immune stimulus exposure as a trigger for the development of chronic pruritus and circulating blood type 2
Jaya Manjunath1,2,3, Viviane Liao1,2,3, Anusha Kambala1,2
1Department of Dermatology, University of Maryland School of Medicine, Baltimore, Maryland.
Background:
Chronic pruritus (CP) is a poorly characterized condition associated with intense pruritus without a primary skin eruption. This condition tends to emerge more commonly in older adults, and there is limited research on triggering factors.
Objective:
To explore the clinical characteristics and pathophysiology of CP following exposure to an immune stimulus.
Methods:
Clinical characteristics and plasma samples were collected from 15 patients who developed CP following an immune stimulus such as checkpoint inhibitors or vaccination. A multiplex panel was used to analyze plasma cytokine concentrations within these patients.
Results:
Most immunotherapy-treated patients experienced CP during treatment or after 21 to 60 days of receiving treatment, while vaccine-stimulated patients developed pruritus within a week of vaccination. Plasma cytokine analysis revealed elevated levels of 12 cytokines in patients with immune-stimulated CP compared to healthy controls. Notably, T helper 2 (Th2) related cytokines interleukin (IL)-5 (fold change 2.65; q < 0.25) and thymic stromal lymphopoietin (fold change 1.61 q < 0.25) were upregulated.
Limitations:
Limitations of this study include limited sample size, particularly in the plasma cytokine assay.
Conclusions And Relevance:
This study reveals triggers of CP development and describes alterations in blood Th2 markers in patients with CP, including IgE, increased blood eosinophils, and cytokines IL-5 and thymic stromal lymphopoietin.
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