TY - JOUR
T1 - New insights into the taxonomy of autoimmune diseases based on polyautoimmunity
AU - Rojas, Manuel
AU - Ramírez-Santana, Carolina
AU - Acosta-Ampudia, Yeny
AU - Monsalve, Diana M.
AU - Rodriguez-Jimenez, Mónica
AU - Zapata, Elizabeth
AU - Naranjo-Pulido, Angie
AU - Suárez-Avellaneda, Ana
AU - Ríos-Serna, Lady J.
AU - Prieto, Carolina
AU - Zambrano-Romero, William
AU - Valero, María Alejandra
AU - Rodríguez, Yhojan
AU - Mantilla, Rubén D.
AU - Zhu, Chengsong
AU - Li, Quan Zhen
AU - Toro-Gutiérrez, Carlos Enrique
AU - Tobón, Gabriel J.
AU - Anaya, Juan Manuel
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/1
Y1 - 2022/1
N2 - Objective: The clinical coexistence of two or more autoimmune diseases (ADs) fulfilling classification criteria is termed “overt polyautoimmunity” (PolyA), whereas the presence of autoantibodies unrelated to an index AD, without clinical criteria fulfillment, is known as “latent PolyA”. We aimed to explore a new taxonomy of ADs based on PolyA. Methods: In a cross-sectional study of 292 subjects, we evaluated the presence of PolyA in 146, 45, 29, 17, and 17 patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), autoimmune thyroid disease (AITD) and systemic sclerosis (SSc), respectively, and 38 healthy controls. Clinical assessment, autoantibody profile (by autoantigen array chip), lymphocytes immunophenotype and cytokine profile (by flow cytometry) were evaluated simultaneously. A mixed cluster methodology was used to classify ADs. Results: Latent PolyA was more frequent than overt PolyA, ranging from 69.9% in RA to 100% in SSc. Nevertheless, both latent and overt PolyA clustered together. Over-expressed IgG autoantibodies were found to be hallmarks for the identification of index ADs. The combination of autoantibodies allowed high accuracy in the classification of ADs. Three well-defined clusters based on PolyA were observed with distinctive clinical and immunological phenotypes. Conclusions: This proof-of-concept study indicates that ADs can be classified according to PolyA. PolyA should be considered in all studies dealing with ADs, including epidemiological, genetic, and clinical trials.
AB - Objective: The clinical coexistence of two or more autoimmune diseases (ADs) fulfilling classification criteria is termed “overt polyautoimmunity” (PolyA), whereas the presence of autoantibodies unrelated to an index AD, without clinical criteria fulfillment, is known as “latent PolyA”. We aimed to explore a new taxonomy of ADs based on PolyA. Methods: In a cross-sectional study of 292 subjects, we evaluated the presence of PolyA in 146, 45, 29, 17, and 17 patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), autoimmune thyroid disease (AITD) and systemic sclerosis (SSc), respectively, and 38 healthy controls. Clinical assessment, autoantibody profile (by autoantigen array chip), lymphocytes immunophenotype and cytokine profile (by flow cytometry) were evaluated simultaneously. A mixed cluster methodology was used to classify ADs. Results: Latent PolyA was more frequent than overt PolyA, ranging from 69.9% in RA to 100% in SSc. Nevertheless, both latent and overt PolyA clustered together. Over-expressed IgG autoantibodies were found to be hallmarks for the identification of index ADs. The combination of autoantibodies allowed high accuracy in the classification of ADs. Three well-defined clusters based on PolyA were observed with distinctive clinical and immunological phenotypes. Conclusions: This proof-of-concept study indicates that ADs can be classified according to PolyA. PolyA should be considered in all studies dealing with ADs, including epidemiological, genetic, and clinical trials.
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U2 - 10.1016/j.jaut.2021.102780
DO - 10.1016/j.jaut.2021.102780
M3 - Research Article
C2 - 34923432
AN - SCOPUS:85121249866
SN - 0896-8411
VL - 126
SP - 1
EP - 14
JO - Journal of Autoimmunity
JF - Journal of Autoimmunity
M1 - 102780
ER -