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大鼠实验性隐球菌病中的免疫抑制。向非相关抗原诱导传出性T抑制细胞。

Immunosuppression in experimental cryptococcosis in rats. Induction of efferent T suppressor cells to a non-related antigen.

作者信息

Masih D T, Sotomayor C E, Rubinstein H R, Riera C M

机构信息

Departamento de Bioquimica Clinica, Facultad de Ciencias, Quimicas, Universidad Nacional de Cordoba, Argentina.

出版信息

Mycopathologia. 1991 Jun;114(3):179-86. doi: 10.1007/BF00437212.

Abstract

Using a rat model, we have previously demonstrated that infection with Cryptococcus neoformans can trigger the production of a series of suppressor cells that specifically inhibit the cell-mediated immune response to a non-related antigen, human serum albumin (HSA), that has been injected 7 days after the infection. We previously determined that the cryptococcal infection induces afferent suppressor or suppressor induction cells (Ts1) to HSA. The primary objective of the present study was to investigate the suppressor cells involved in the efferent phase of delayed-type hypersensitivity (DTH) response to HSA in rats infected with C. neoformans and immunized with the non-related antigen and determine the role that the Ts1 cell plays in the induction of that cell. For this purpose, the spleen mononuclear (SpM) cells containing the Ts1 or SpM cells from immunized non-infected rats (used as donor controls) were transferred to two groups of syngeneic naive recipients (first recipients). Later, the SpM cells from both groups of animals were transferred to rats immunized with HSA (second recipients). The efferent limb of the DTH response to HSA was suppressed in the recipients that received SpM cells from donors injected with Ts1 cells. Additional HSA antigen was not required for induction of these efferent suppressor cells. Furthermore, we here show that these cells are resistant to treatment with cyclophosphamide (Cy), and that they can activate another suppressor population. The latter are Cy sensitive and are present in the immune recipient.

摘要

我们先前利用大鼠模型证明,新型隐球菌感染可触发一系列抑制细胞的产生,这些抑制细胞能特异性抑制对一种无关抗原——人血清白蛋白(HSA)的细胞介导免疫反应,该抗原在感染7天后注射。我们先前确定,隐球菌感染可诱导针对HSA的传入抑制细胞或抑制诱导细胞(Ts1)。本研究的主要目的是调查感染新型隐球菌并用无关抗原免疫的大鼠中,参与对HSA迟发型超敏反应(DTH)传出阶段的抑制细胞,并确定Ts1细胞在该细胞诱导过程中所起的作用。为此,将含有Ts1的脾单核细胞(SpM)或来自免疫未感染大鼠的SpM细胞(用作供体对照)转移到两组同基因的未免疫受体(第一受体)。之后,将两组动物的SpM细胞转移到用HSA免疫的大鼠(第二受体)。接受来自注射Ts1细胞的供体的SpM细胞的受体中,对HSA的DTH反应的传出支被抑制。诱导这些传出抑制细胞不需要额外的HSA抗原。此外,我们在此表明,这些细胞对环磷酰胺(Cy)治疗有抗性,并且它们可以激活另一个抑制细胞群体。后者对Cy敏感,存在于免疫受体中。

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