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Updated: Jul 11, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Autoinflammatory syndromes: inborn errors of natural immunity]
Matteo Colina1, Marcello Govoni, Francesco De Leonardis
1Sezione di Reumatologia, Dipartimento di Medicina Clinica e Sperimentale, Università, Ferrara. teocolina@libero.it
Abstract:
The notion of autoinflammatory diseases delineates a heterogenous group of genetic pathologies characterized by spontaneous periodic systemic inflammation in the absence of infectious or autoimmune causes. The general hypothesis is that the innate immune response in these patients is wrongly tuned, being either too sensitive to minor stimuli or turned off too late. Clinical pictures of these disorders are characterized by high spiking fever associated with involvement of musculo-skeletal system, tegumentary apparatus and serosas. Although inflammatory syndromes are considered rare, they may represent a model in order to unravel some aspects of the innate immune system and of the inflammatory cascade.
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