Publication:
MASS CYTOMETRY DATA RECLASSIFY SYSTEMIC AUTOIMMUNE DISEASE PATIENTS IN PHENOTYPICALLY DISTINCTIVE GROUPS

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Date

2022-06-01

Authors

Rybakowska, P.
van Gassen, S.
Perez-Sanchez, C.
Ibanez-Costa, A.
Varela, N.
Castro, R. Ortega
Fernandez-Roldan, C.
Jimenez-Moleon, I.
Ortego, N.
Raya, E.

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BMJ Group
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Abstract

Systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), systemic sclerosis (SSC), Sjögren’s syndrome (SJS), mixed connective tissue disease (MCTD), primary antiphospholipid syndrome (PAPS) and undifferentiated connective tissue disease (UCTD) are classified as systemic autoimmune diseases (SADs). They are diagnosed based on different clinical and laboratory criteria. Due to their high internal heterogeneity and overlapping symptoms, SADs are difficult to diagnose. Therefore, molecular and cellular-based studies need to be undertaken to precisely classify the patients. Mass cytometry is a single-cell proteomics technology that measures approximately 50 markers per cell, thus it is a suitable tool to perform deep-phenotyping studies in SADs.

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MeSH Terms

Lupus erythematosus, systemic
Arthritis, rheumatoid
Scleroderma, systemic
Humans

DeCS Terms

Artritis reumatoide
Esclerodermia sistémica
Humanos
Lupus eritematoso sistémico

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Keywords

Antiphospholipid syndrome, Mixed connective tissue disease, Undifferentiated connective tissue diseases, Proteomics

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