2021
DOI: 10.1111/imj.15448
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Systemic lupus erythematosus: a clinical update

Abstract: Systemic lupus erythematosus (SLE) is a multi-system autoimmune disease known for its complexity and heterogeneity. Striking diversity can be observed between individual patients, in terms of clinical manifestations, serological abnormalities, disease progression and response to therapy. Furthermore, dysfunction of a broad range of immune pathways underlies disease development and expression. An appreciation of this diversity is vital in order to diagnose accurately and appropriately treat patients with SLE as… Show more

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Cited by 9 publications
(3 citation statements)
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“…Anti-phospholipid antibodies are found in 29–46% of SLE patients, and up to 50% of them may have pregnancy morbidity or arterial or venous thrombosis. [ 102 ]. The condition has a hereditary component, with 24–35 percent concordance in monozygotic twins and 2–5% in dizygotic twins.…”
Section: T1dmand Autoimmune Endocrine Pathologymentioning
confidence: 99%
“…Anti-phospholipid antibodies are found in 29–46% of SLE patients, and up to 50% of them may have pregnancy morbidity or arterial or venous thrombosis. [ 102 ]. The condition has a hereditary component, with 24–35 percent concordance in monozygotic twins and 2–5% in dizygotic twins.…”
Section: T1dmand Autoimmune Endocrine Pathologymentioning
confidence: 99%
“…The current study is consistent with prior research findings indicating that SLE can be present at any age (9) . it is most frequently diagnosed between ages 15 and 45 (10) .…”
Section: Discussionmentioning
confidence: 99%
“…To date, the management of SLE has moved from conventional treatments to biological treatments to decrease the risk of progressive irreversible damage accrual and increased mortality in patients with this chronic disease [99]. Immunomodulation and immunosuppressive state are being considered for SLE therapeutic approaches [100,101]. In our results, the augmented IL-10 secretion from C. glabrata β-glucans stimulated-dendritic cells may be used and adapted for the biological therapies in SLE.…”
Section: Expression Of T Cells From Splenocytes and Lymph Node Cells ...mentioning
confidence: 78%