The effects of pregnancy on myelin basic protein-induced experimental autoimmune encephalomyelitis in Lewis rats: suppression of clinical disease, modulation of cytokine expression in the spinal cord inflammatory infiltrate and suppression of lymphocyte proliferation by pregnancy sera.

J. Harness, P. Mccombe
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引用次数: 7

Abstract

PROBLEM The present study was performed to explore the effects of pregnancy on experimental autoimmune encephalomyelitis (EAE) induced in Lewis rats by inoculation with myelin basic protein (MBP) (MBP-EAE). METHOD OF STUDY MBP-EAE was induced in pregnant and non-pregnant rats and severity of disease evaluated. Serum from pregnant and non-pregnant rats was used in standard lymphocyte proliferation assays. Real-time polymerase chain reaction (PCR) was used to investigate the expression of cytokine mRNA in the inflammatory cells obtained from the spinal cord of rats on day 15 after inoculation. RESULTS Pregnant rats developed less severe disease than non-pregnant rats. Serum from pregnant rats suppressed the proliferation of T lymphocytes in response to MBP. There was significantly increased expression of IL-4, IL-10 and TNF-alpha mRNA in the spinal cord infiltrate of pregnant rats. CONCLUSION Circulating humoral factors and alteration in cytokine production by inflammatory cells may contribute to the suppression of EAE in pregnant rats.
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妊娠对髓鞘碱性蛋白诱导的Lewis大鼠实验性自身免疫性脑脊髓炎的影响:妊娠血清对临床疾病的抑制、对脊髓炎症浸润细胞因子表达的调节以及对淋巴细胞增殖的抑制。
本研究旨在探讨妊娠对接种髓鞘碱性蛋白(MBP)诱导Lewis大鼠实验性自身免疫性脑脊髓炎(EAE)的影响。方法:采用妊娠大鼠和非妊娠大鼠诱导bp - eae,并评价其病变严重程度。用妊娠和非妊娠大鼠血清进行标准淋巴细胞增殖试验。采用实时聚合酶链反应(Real-time polymerase chain reaction, PCR)检测接种后第15天大鼠脊髓炎症细胞中细胞因子mRNA的表达。结果妊娠大鼠发病严重程度低于未妊娠大鼠。妊娠大鼠血清对MBP有抑制T淋巴细胞增殖的作用。妊娠大鼠脊髓浸润中IL-4、IL-10和tnf - α mRNA的表达显著升高。结论妊娠大鼠EAE的抑制可能与循环体液因子及炎症细胞产生细胞因子的改变有关。
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Issue Information Program Participants Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage. Pro-inflammatory maternal cytokine profile in preterm delivery. The immune environment in human endometrium during the window of implantation.
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