2019
DOI: 10.1016/j.clim.2018.10.009
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2B4 (CD244, SLAMF4) and CS1 (CD319, SLAMF7) in systemic lupus erythematosus and cancer

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Cited by 19 publications
(15 citation statements)
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“…Moreover, SLE patients have decreased expression of CD244 in monocytes and NK cells. Other research of CD244-deficient mice showed that regulation of NK cells by CD244 might be related to the gender-specific immune response in SLE (41,47,48). Genetic studies indicated that a single nucleotide polymorphism (SNP) in CD244 was related to SLE susceptibility, and that alternative splicing of the CD244 mRNA also regulated SLE progression (49,50).…”
Section: Systemic Lupus Erythematosusmentioning
confidence: 99%
See 1 more Smart Citation
“…Moreover, SLE patients have decreased expression of CD244 in monocytes and NK cells. Other research of CD244-deficient mice showed that regulation of NK cells by CD244 might be related to the gender-specific immune response in SLE (41,47,48). Genetic studies indicated that a single nucleotide polymorphism (SNP) in CD244 was related to SLE susceptibility, and that alternative splicing of the CD244 mRNA also regulated SLE progression (49,50).…”
Section: Systemic Lupus Erythematosusmentioning
confidence: 99%
“…However, research has also indicated a number of unresolved problems regarding CD244. For example, studies of SLE patients showed that CD244 had different regulatory effects in the same type of immune cells (CD8 + T cells) (46,47); some studies attributed this difference to the different regulatory effects of CD244 by different cell subtypes. However, this problem is not so simply resolved because CD244 also has different regulatory effects on virus-specific T cells in two diseases caused by HTLC-1 (ATL and HAM/TSP), and had adverse effects in both cases.…”
Section: Conclusion and Prospectmentioning
confidence: 99%
“…The role of CD48 as a costimulatory receptor of various immune responses is still being studied. The previous papers concentrated mainly on autoimmune diseases such as systemic sclerosis [18] or systemic lupus erythematosus [19], cancer (multiple myeloma [19] and acute myeloid leukemia [20]), and bacterial and other infectious diseases [21]. Interactions between CD48 and CD244 (2B4) on mast cells, eosinophils, and basophils suggest that these cell types can act synergistically in the “allergic effector unit” to promote inflammation.…”
Section: Discussionmentioning
confidence: 99%
“…Unveiling these mechanisms and events is required to identify new immunological cellular biomarkers, trace disease progression, and design new targeted therapeutic strategies for autoimmunity. In this scenario, re-education/manipulation of NK cells appear as a promising strategy, as confirmed by the growing interest in CAR-NK cells ( 136 ).…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 94%