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参与对大鼠雄性附属性腺自身免疫反应调节的细胞。

Cells involved in the regulation of the autoimmune response to rat male accessory glands.

作者信息

Rivero V E, Iribarren P, Riera C M

机构信息

Departamento de Bioquímica Clínca, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.

出版信息

Braz J Med Biol Res. 1994 Nov;27(11):2579-89.

PMID:7549980
Abstract
  1. The immunization of Wistar rats with 5 mg of chemically modified rat male accessory glands saline extract (MRAG) incorporated into complete Freund's adjuvant (CFA) induced a delayed type hypersensitivity (DTH) response to rat male accessory glands (RAG). Pretreatment with peritoneal cells (PC) obtained from rats 2 h after an intraperitoneal (ip) injection of a partially purified fraction (FI) of RAG (FI-PC2h) suppressed the DTH response to MRAG after immunization with MRAG-CFA, while pretreatment with PC obtained 24 h after an ip injection of FI-RAG (FI-PC24h) induced potentiation of the DTH response to MRAG. 2. The injection of spleen mononuclear cells (SpM), obtained from rats rendered unresponsive to MRAG by pretreatment with FI-PC2h, into normal syngeneic recipients markedly prevented the DTH reaction to MRAG. The transfer of SpM cells from animals injected with FI-PC24h (potentiated animals) to suppressed recipients (recipients of FI-PC2h on days -10 and -3, prior to immunization with MRAG-CFA) showed that SpM cells did not eliminate the suppression state in these recipients, but when they were transferred to normal recipients, they were able to induce a positive response to RAG (P < 0.005). 3. The study of the phenotypic characteristics of the SpM cells prior to transfer showed similar numbers of CD4 and IL-2R SpM cells in both potentiated and normal animals. However, the number of CD8 cells was significantly reduced in SpM cells from potentiated animals compared to that observed in SpM cells from normal animals (P < 0.05).
摘要
  1. 用5毫克化学修饰的大鼠雄性副性腺盐水提取物(MRAG)与完全弗氏佐剂(CFA)混合对Wistar大鼠进行免疫,可诱导对大鼠雄性副性腺(RAG)的迟发型超敏反应(DTH)。用腹腔注射部分纯化的RAG组分(FI)后2小时从大鼠获得的腹腔细胞(PC)进行预处理(FI-PC2h),在用MRAG-CFA免疫后可抑制对MRAG的DTH反应,而用腹腔注射FI-RAG后24小时获得的PC进行预处理(FI-PC24h)则可诱导对MRAG的DTH反应增强。2. 用FI-PC2h预处理使大鼠对MRAG无反应后,从这些大鼠获得的脾单核细胞(SpM)注射到正常同基因受体中,可显著预防对MRAG的DTH反应。将注射了FI-PC24h的动物(增强动物)的SpM细胞转移到受抑制的受体(在免疫MRAG-CFA前第-10天和第-3天接受FI-PC2h的受体)中,结果表明SpM细胞并未消除这些受体中的抑制状态,但当将它们转移到正常受体中时,它们能够诱导对RAG的阳性反应(P<0.005)。3. 转移前对SpM细胞表型特征的研究表明,在增强动物和正常动物中,CD4和IL-2R SpM细胞的数量相似。然而,与正常动物的SpM细胞相比,增强动物的SpM细胞中CD8细胞的数量显著减少(P<0.05)。

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