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Cifuentes RA, Restrepo-Montoya D, Anaya JM. The autoimmune tautology: an in silico approach. Autoimmune Dis. 2012;2012:792106doi: 10.1155/2012/792106.
Cifuentes, R. A., Restrepo-Montoya, D., & Anaya, J. M. (2012). The autoimmune tautology: an in silico approach. Autoimmune diseases, 2012792106. https://doi.org/10.1155/2012/792106
Cifuentes, Ricardo A, et al. "The autoimmune tautology: an in silico approach." Autoimmune diseases vol. 2012 (2012): 792106. doi: https://doi.org/10.1155/2012/792106
Cifuentes RA, Restrepo-Montoya D, Anaya JM. The autoimmune tautology: an in silico approach. Autoimmune Dis. 2012;2012:792106. doi: 10.1155/2012/792106. Epub 2012 Mar 05. PMID: 22474574; PMCID: PMC3303588.
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Autoimmune Dis. 2012;2012:792106. doi: 10.1155/2012/792106. Epub 2012 Mar 05.

The autoimmune tautology: an in silico approach.

Autoimmune diseases

Ricardo A Cifuentes, Daniel Restrepo-Montoya, Juan-Manuel Anaya

Affiliations

  1. Center for Autoimmune Diseases Research (CREA), School of Medicine and Health Sciences, Universidad del Rosario, Carrera 24, No. 63-69 piso 3, Bogotá, Colombia.

PMID: 22474574 PMCID: PMC3303588 DOI: 10.1155/2012/792106

Abstract

There is genetic evidence of similarities and differences among autoimmune diseases (AIDs) that warrants looking at a general panorama of what has been published. Thus, our aim was to determine the main shared genes and to what extent they contribute to building clusters of AIDs. We combined a text-mining approach to build clusters of genetic concept profiles (GCPs) from the literature in MedLine with knowledge of protein-protein interactions to confirm if genes in GCP encode proteins that truly interact. We found three clusters in which the genes with the highest contribution encoded proteins that showed strong and specific interactions. After projecting the AIDs on a plane, two clusters could be discerned: Sjögren's syndrome-systemic lupus erythematosus, and autoimmune thyroid disease-type1 diabetes-rheumatoid arthritis. Our results support the common origin of AIDs and the role of genes involved in apoptosis such as CTLA4, FASLG, and IL10.

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