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New complex cell junctions in and around the intervertebral discs discovered using autoantibodies from patients affected by endemic pemphigus foliaceus in El Bagre, Colombia, South America.

作者信息

Abreu Velez Ana Maria, Hashimoto Takashi, Vélez Arango Jorge Mario, Upegui-Zapata Yulieth Alexandra, Upegui-Quiceño Eduardo, Aponte Adriana Milena Olarte, Howard Michael S

机构信息

Georgia Dermatopathology Associates, Atlanta, GA, USA.

Department of Dermatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.

出版信息

Int J Dermatol. 2025 Mar;64(3):552-562. doi: 10.1111/ijd.17471. Epub 2024 Sep 15.

DOI:10.1111/ijd.17471
PMID:39279034
Abstract

BACKGROUND

Traditionally, the intervertebral disks' (IVD) nucleus pulposus (NP) and annulus fibrosus (AF) are considered to have few cellular components and cell junctions. Patients affected by a new variant of endemic pemphigus foliaceus in El Bagre, Colombia, experience back pain in the spinal areas of the lower and upper back. Here, we investigate the reactivity of the patient's autoantibodies to structures in and around the IVDs at the cellular level.

METHODS

We first administered a questionnaire and performed a medical examination. We then tested for autoreactivity against IVDs by indirect immunofluorescence, confocal microscopy, and reflectance confocal microscopy using bovine and human tissues as antigen sources. We tested 45 sera from patients affected by the disease and 45 control sera from the endemic area matched by age, gender, demographics, and work activity.

RESULTS

Most of the patient sera revealed polyclonal antibodies against newly discovered cell junctions in the NP and AF, including their translamellar cross-bridges. Additional reactivities were detected against cell junctions in the spinal cord neurons, paraspinal nerves, blood vessels, anterior and posterior longitudinal ligaments, and paraspinal skeletal muscles. The reactivities of the patient's autoantibodies co-localized with those of commercially available antibodies to desmoplakins I-II, armadillo repeat gene deleted in velo-cardio-facial syndrome, plakophilin-4, and myocardium-enriched zonula occludens-1-associated protein (p < 0.001).

CONCLUSIONS

We discovered novel complex cell junctions in the IVDs using patients' autoantibodies. These discoveries open a new chapter in the knowledge of IVD, representing a breakthrough pertinent to many diseases.

摘要

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