This proof-of-concept pilot study highlights the potential for epidural lidocaine injection as an effective and safe therapeutic strategy for psoriasis treatment and expands understanding of the role of the peripheral nerve system in psoriasis and possibly other skin diseases.

Use of an epidural nerve block with lidocaine leads to clearance of psoriatic skin lesions, according to a novel proof-of-concept study in the Journal of Investigative Dermatology.

“Case studies have shown that psoriasis patients have experienced significant symptom relief after receiving epidural anesthesia during surgery, suggesting a pivotal role of the nervous system in psoriasis pathogenesis,” explains lead investigator Honglin Wang, PhD, Shanghai Institute of Immunology, Precision Research Center for Refractory Diseases, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, in a news release. “Additionally, there is increasing evidence linking the neuroimmune connection to psoriasis and other skin diseases. These factors inspired us to explore the possibility of directly targeting the nervous system for psoriasis treatment and the detailed mechanism of neuroimmune crosstalk in psoriasis.”

Investigators conducted a proof-of-concept study using an epidural injection of lidocaine to treat four patients with psoriasis. An epidural catheter was inserted between T12 (i.e., the 12th thoracic vertebra) and L1 (i.e., the first lumbar vertebra) of the spinal cord. Lidocaine solution was injected through the catheter. Each patient received three or four treatments in total. Two patients had psoriatic lesions throughout the whole body; two patients had psoriatic lesions mainly distributed on the legs.

By the end of the study period, all patients achieved remarkable improvements in almost all lesions, showing a 35 percent to 70 percent reduction in Psoriasis Area and Severity Index (PASI) scores. Furthermore, skin improvements were maintained for at least 24 weeks after discontinuation of lidocaine treatment. No adverse effects occurred. This research provides the first clinical evidence that sensory nerves are potential targets for psoriasis treatment.

To evaluate the neuroimmune communication signaling in psoriasis and the mechanism for lidocaine therapy, investigators also conducted a number of experiments on rats in which a psoriasis-like skin inflammation had been induced. They found that lidocaine acts on sensory neurons by downregulating disordered neurite growth and proinflammatory CGRP (calcium gene-related peptide) release. Concomitantly, restricted CGRP+ nerve density leads to reduced IL-23 production from dendritic cells, which express excessive CGRP receptors.

In summary, this proof-of-concept pilot study highlights the potential for epidural lidocaine injection as an effective and safe therapeutic strategy for psoriasis treatment and expands understanding of the role of the peripheral nerve system in psoriasis and possibly other skin diseases. Manipulating the neuroimmune interplay puts a brake on neurogenic inflammation and downstream key inflammatory cytokine production, providing therapeutic prospects for sensory neuron‒orchestrated inflammatory skin diseases.

“Epidural lidocaine therapy provides a novel choice for patients who respond poorly to the current treatment modalities for psoriasis,” adds lead author Qianqian Yin, PhD, Shanghai Institute of Immunology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

“Although these findings are promising, this was a small pilot study that lacks a placebo-controlled arm and controls to prevent interference by environmental changes. We next need to conduct large-scale clinical studies,” comments co-investigator Libo Sun, PhD, Shanghai Institute of Immunology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

PHOTO CAPTION: Epidural lidocaine treatment has a beneficial therapeutic effect on patients with moderate-to-severe psoriasis.

PHOTO CREDIT: Journal of Investigative Dermatology