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口服耐受与淋巴细胞活性水平高相关。

Oral tolerance correlates with high levels of lymphocyte activity.

机构信息

Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Cell Immunol. 2012 Dec;280(2):171-81. doi: 10.1016/j.cellimm.2012.12.004. Epub 2013 Jan 5.

Abstract

Oral tolerance is defined as an inhibition of specific immune responsiveness to a previously ingested antigen. Paradoxically, we found an increased lymphocyte activity in tolerant mice alongside the specific inhibition. Orally-tolerant mice presented higher number of immunoglobulin secreting cells (ISC) in spleen and bone marrow; showed a greater variety of Ig classes being produced: IgM and IgA in the spleen and IgG and IgM in the bone marrow. ISC from immunized mice produced mainly IgG. Despite having the same number of regulatory and activated T cells in the spleen after immunization, these cells appeared earlier in tolerant mice, right after the primary immunization. Also, tolerant mice showed a prompt expression of regulatory cytokines (TGF-β and IL-10) and a transient expression of effector cytokines (IL-2 and IFN-γ). Thus, in addition to an inhibited specific responsiveness, orally-tolerant mice displayed an early and widespread mobilization of activated and regulatory lymphocytes.

摘要

口服耐受是指对先前摄入的抗原产生特异性免疫应答抑制。矛盾的是,我们发现耐受小鼠的淋巴细胞活性增加,同时存在特异性抑制。口服耐受小鼠的脾脏和骨髓中分泌免疫球蛋白的细胞(ISC)数量增加;产生的 Ig 类更多:脾脏中产生 IgM 和 IgA,骨髓中产生 IgG 和 IgM。免疫小鼠的 ISC 主要产生 IgG。尽管在免疫后脾脏中的调节和活化 T 细胞数量相同,但这些细胞在耐受小鼠中更早出现,就在初次免疫后。此外,耐受小鼠表现出调节细胞因子(TGF-β 和 IL-10)的快速表达和效应细胞因子(IL-2 和 IFN-γ)的短暂表达。因此,除了受到抑制的特异性反应外,口服耐受小鼠还表现出活化和调节性淋巴细胞的早期和广泛动员。

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