AI Article Synopsis

  • Pure Neural Leprosy (PNL) is a rare form of leprosy that specifically impacts the peripheral nervous system, and its underlying mechanisms are not well understood.
  • A study of 30 PNL patients revealed high rates of neural thickening, sensory symptoms, and neuropathic pain, as well as distinct cytokine profiles that differ from other leprosy forms.
  • The findings suggest that cytokines like CCL-2 and IL-10 play significant roles in PNL, potentially influencing silent neuritis and overall disease understanding, highlighting the need for further research on its immunological aspects.

Article Abstract

Introduction: Pure Neural Leprosy (PNL) is a form of this long time known disease that affects only the peripheral nervous system. Since it is a rare form of the disease, its pathophisiology is still poorly understood.

Objective: Describe the cytokines profile in patients with PNL.

Methods: 30 Patients diagnosed with PNL in the Souza Araujo Outpatient Clinic and with cytokines evaluated were selected. They were evaluated by neurologists and diagnosed after a nerve biopsy. Serum levels of IL-1 β, IL-6, IL-10, IL-17, TNF, CCL-2/MCP-1, IFN-ϒ, CXCL-10/IP-10 and TGF-β were evaluates at the moment of the diagnosis.

Results: Neural thickening was a common clinical finding in this groups of patients. Small and medium sensitive fibers signs and symptoms were present in 92% of the patients and motor involvement in 53%. 43% of patients presented neuropathic pain and no one had neuritis TGF-beta, IL-17, CCl-2 and IP-10. CCL-2 levels were associated with demyelinating patters and IP-10 and IL-1o were associated with axonal patterns at NCS.

Discussion: PNL patients' cytokine profile appears to be different of other clinical forms of leprosy, with the presence of cytokines described in both tuberculoid and lepromatous leprosy. High levels of CCl-2 may be related to the presence of silent neuritis as well as the presence of IL-10. PNL is unique a form of leprosy, therefore, understanding its immunological profiles essential to better understand the disease itself.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10728593PMC
http://dx.doi.org/10.3389/fimmu.2023.1272471DOI Listing

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