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在维生素A缺乏期间,视黄酸和聚肌苷酸协同作用以增强对破伤风类毒素的抗体反应:白细胞介素-2受体β、信号转导和转录激活因子-1以及干扰素调节因子-1可能参与其中。

Retinoic acid and polyriboinosinic acid act synergistically to enhance the antibody response to tetanus toxoid during vitamin A deficiency: possible involvement of interleukin-2 receptor-beta, signal transducer and activator of transcription-1, and interferon regulatory factor-1.

作者信息

DeCicco K L, Zolfaghari R, Li N q, Ross A C

机构信息

Department of Nutrition, Pennsylvania State University, University Park, Pennsylvania, USA.

出版信息

J Infect Dis. 2000 Sep;182 Suppl 1:S29-36. doi: 10.1086/315908.

Abstract

Antibody responses to T cell-dependent antigens are reduced during vitamin A (VA) deficiency and restored by retinoids. To test whether retinoic acid (RA) and polyinosinic:polycytidylic acid (PIC), an inducer of interferons, can increase specific antibody production, VA-deficient rats were treated with all-trans-RA, PIC, or both at the time of primary immunization with tetanus toxoid. VA-deficient rats produced low primary and secondary anti-tetanus IgG responses (P<.001 vs. VA-sufficient controls). Both responses were increased synergistically by RA plus PIC (P<.0001). In VA-deficient spleens, mRNAs were low for interleukin (IL)-2 receptor-beta, interferon regulatory factor-1, and signal transducer and activator of transcription 1. Each, however, was induced by RA plus PIC (P<.0001 vs. controls). Conversely, IL-12 and IL-10 mRNAs were elevated in VA deficiency and were induced by PIC and suppressed by RA. Thus, RA plus PIC appears to be a promising combination for stimulating antigen-specific immunity. Several molecular factors identified here may partially account for the observed enhancement.

摘要

在维生素A(VA)缺乏期间,对T细胞依赖性抗原的抗体反应会降低,而类视黄醇可使其恢复。为了测试视黄酸(RA)和多聚肌苷酸:多聚胞苷酸(PIC,一种干扰素诱导剂)是否能增加特异性抗体的产生,在用破伤风类毒素进行初次免疫时,对VA缺乏的大鼠给予全反式视黄酸、PIC或两者。VA缺乏的大鼠产生的初次和二次抗破伤风IgG反应较低(与VA充足的对照组相比,P<0.001)。RA加PIC可使这两种反应协同增加(P<0.0001)。在VA缺乏的脾脏中,白细胞介素(IL)-2受体β、干扰素调节因子-1以及信号转导和转录激活因子1的mRNA水平较低。然而,RA加PIC均可诱导这些mRNA的表达(与对照组相比,P<0.0001)。相反,IL-12和IL-10的mRNA在VA缺乏时升高,PIC可诱导其表达,而RA可抑制其表达。因此,RA加PIC似乎是刺激抗原特异性免疫的一种有前景的组合。这里确定的几个分子因素可能部分解释了观察到的增强作用。

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