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Review
. 2013 Aug;12(10):967-71.
doi: 10.1016/j.autrev.2013.02.003. Epub 2013 Mar 26.

Assessment of intracellular cytokines and regulatory cells in patients with autoimmune diseases and primary immunodeficiencies - novel tool for diagnostics and patient follow-up

Affiliations
Review

Assessment of intracellular cytokines and regulatory cells in patients with autoimmune diseases and primary immunodeficiencies - novel tool for diagnostics and patient follow-up

Liv T Osnes et al. Autoimmun Rev. 2013 Aug.

Abstract

Serum and intracytoplasmic cytokines are mandatory in host defense against microbes, but also play a pivotal role in the pathogenesis of autoimmune diseases by initiating and perpetuating various cellular and humoral autoimmune processes. The intricate interplay and fine balance of pro- and anti-inflammatory processes drive, whether inflammation and eventually organ damage will occur, or the inflammatory cascade quenches. In the early and late, as well as inactive and active stages of autoimmune diseases, different cellular and molecular patterns can dominate in these patients. However, the simultaneous assessment of pro- and anti-inflammatory biomarkers aids to define the immunological state of a patient. A group of the most useful inflammatory biomarkers are cytokines, and with increasing knowledge during the last decade their role have been well-defined in patients with autoimmune diseases and immunodeficiencies. Multiple pathological processes drive the development of autoimmunity and immunodeficiencies, most of which involve quantitative and qualitative disturbances in regulatory cells, cytokine synthesis and signaling pathways. The assessment of these biomarkers does not aid only in the mechanistic description of autoimmune diseases and immunodeficiencies, but further helps to subcategorize diseases and to evaluate therapy responses. Here, we provide an overview, how monitoring of cytokines and regulatory cells aid in the diagnosis and follow-up of patients with autoimmune diseases and immunodeficiencies furthermore, we pinpoint novel cellular and molecular diagnostic possibilities in these diseases.

Keywords: AIRE; Alipoprotein A1; ApoA1; Autoimmune diseases; Breg; CFS; CVID; ECP; EPO; G-CSF; HGF; IFN; IL; IL-1Ra; IPEX; Immunodeficiencies; Immunoregulatory abnormalities; MCTD; ME; NK; NKT; PID; PM/DM; Primary immunodeficiency; RA; RAG; Regulatory T cells; SCID; SLE; SNHL; SS; SSc; Sjögren's syndrome; Soluble, intracellular cytokines; T-cytotoxic cell; T-helper cell; TNF; TPO; Tc; Th; Th17 cells; Treg; Tumor necrosis factor; U1 ribonucleoprotein; U1RNP; UCTD; autoimmune regulator; chronic fatigue syndrome; common variable immunodeficiency; erythropoietin; extracorporeal photochemotherapy; granulocyte colony-stimulating factor; hepatocyte growth factor; iTreg; immunodysregulation polyendocrinopathy enteropathy X-linked syndrome; induced regulatory T cell; interferon; interleukin; interleukin-1 receptor alpha; mixed connective tissue disease; myalgic encephalitis; nTreg; natural killer T cell; natural killer cell; natural regulatory T cell; polymyositis/dermatomyositis; recombination activating genes; regulatory B cell; regulatory T cell; rheumatoid arthritis; sensorineural hearing loss; severe combined immunodeficiency; systemic lupus erythematosus; systemic sclerosis; thrombopoietin; undifferentiated connective tissue disease.

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