2014
DOI: 10.1007/s10517-014-2533-x
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Semaforin Sema4D in the Immune System in Multiple Sclerosis

Abstract: The expression of class IV semaforin Sema4D and its CD72 receptor on lymphocytes was studied in patients with multiple sclerosis. The disease was associated with an increase in Sema4D level on intact T lymphocytes and with its more intense shedding from the membrane of activated cell. Multiple sclerosis was also associated with a decrease of CD72 receptor expression by B lymphocytes. Possible contribution of Sema4D to the disease development via the direct effects in the CNS and the immunomodulatory effect, sp… Show more

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Cited by 15 publications
(7 citation statements)
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“…Investigation of the expression of CD100 on lymphocytes revealed disease associated increase in CD100 on T lymphocytes and shedding from the membrane of activated T cells in multiple sclerosis (MS). MS was also associated with a decrease of CD72 receptor expression by B lymphocytes suggesting a possible contribution of CD100 to the disease development via the direct effects in the CNS and the immunomodulatory effect on B cell activity regulation (Kuklina et al 2014). Modulation of B cell regulatory molecules CD22 and CD72 in myasthenia gravis (MG) and MS has been reported by Lu et al (2013).…”
Section: Functional Effects and Disease Associations Of Human Cd72mentioning
confidence: 87%
“…Investigation of the expression of CD100 on lymphocytes revealed disease associated increase in CD100 on T lymphocytes and shedding from the membrane of activated T cells in multiple sclerosis (MS). MS was also associated with a decrease of CD72 receptor expression by B lymphocytes suggesting a possible contribution of CD100 to the disease development via the direct effects in the CNS and the immunomodulatory effect on B cell activity regulation (Kuklina et al 2014). Modulation of B cell regulatory molecules CD22 and CD72 in myasthenia gravis (MG) and MS has been reported by Lu et al (2013).…”
Section: Functional Effects and Disease Associations Of Human Cd72mentioning
confidence: 87%
“…In patients with Systemic Lupus Erythematosus, low expression of CD72 on B cells is negatively correlated with patient disease activity (SLEDAI) ( 28 ). CD72 is lowly expressed in multiple sclerosis and its ligand CD100 is increased in T cells ( 29 ). CD72 is lowly expressed in NPC tissues, suggesting that our low CD72 expression may be related to poor prognosis in NPC patients.…”
Section: Discussionmentioning
confidence: 99%
“…The involvement of B lymphocytes has been increasingly recognized in the occurrence of primary Sjogren's Syndrome (pSS) [6]. And CD72, being a coreceptor of B cell receptor (BCR), has been reported to be an important regulator in the pathogenesis of several autoimmune diseases [20][21][22][23]25]. However, the role of CD72 in pSS has been rarely studied [24].…”
Section: Discussionmentioning
confidence: 99%
“…In SLE patients, the lower expression of CD72 on B cells was inversely associated with patients' disease activity (SLEDAI) and correlated with the presence of lupus nephritis, anti-dsDNA antibodies and low levels of complement [20]. In multiple sclerosis, the expression of CD72 decreased along with an increase in expression of its ligand CD100 on T cells and abnormal levels of several inflammatory factors [22,23]. Conversely, CD72 expression was upregulated on CD19 + CD27+ memory B cells in immune thrombocytopenia (ITP), and was associated with platelet count and anti-platelet antibodies [25].…”
Section: Discussionmentioning
confidence: 99%
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