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通过皮内注射编码B细胞恶性肿瘤中免疫球蛋白重链人类可变区基因序列的裸DNA诱导体液和细胞抗独特型免疫。

Induction of humoral and cellular anti-idiotypic immunity by intradermal injection of naked DNA encoding a human variable region gene sequence of an immunoglobulin heavy chain in a B cell malignancy.

作者信息

Abe A, Emi N, Taji H, Kasai M, Kohno A, Saito H

机构信息

First Department of Internal Medicine, Nagoya University School of Medicine, Japan.

出版信息

Gene Ther. 1996 Nov;3(11):988-93.

PMID:8940639
Abstract

The idiotypic determinants of a B cell neoplasia could provide a tumor-specific target for vaccinating patients against their B cell tumors. Several approaches for inducing idiotype-specific immunization have been reported, but their major theoretical focus was related to the induction of humoral immunity. We have investigated an immunization procedure with naked DNA encoding human variable region gene sequences of an immunoglobulin heavy chain (VH), which may generate both humoral and cellular immune responses against the idiotype of a B cell acute lymphoblastic leukemia (ALL). Using polymerase chain reaction (PCR) amplification, we investigated heavy chain variable region genes obtained from an ALL patient and whether they could induce humoral and cellular immune responses in DBA/2 mice. The VH sequence was cloned into a mammalian expression vector for intradermal DNA vaccination and into a bacterial expression vector to obtain VH protein for Western blotting. The mammalian expression vector encoding the VH gene was injected into mice three times at 7-day intervals and was transduced into P1HTR which is a syngeneic tumor of DBA/2, to serve as target cells to detect cellular immunity. Spleen cells from the inoculated mice exhibited a significant cytotoxic T lymphocyte response to the target cells. By Western blotting, we could also detect trace levels of anti-VH antibodies in all mice serum. This approach for the induction of cellular immunity by intradermal injection is easy and variable region-specific, and may be used as vaccines after chemotherapy treatment of B cell malignancies.

摘要

B细胞肿瘤的独特型决定簇可为针对患者B细胞肿瘤进行疫苗接种提供肿瘤特异性靶点。已有多种诱导独特型特异性免疫的方法被报道,但它们主要的理论重点与体液免疫的诱导有关。我们研究了一种用编码免疫球蛋白重链(VH)人类可变区基因序列的裸DNA进行免疫的程序,该程序可能产生针对B细胞急性淋巴细胞白血病(ALL)独特型的体液免疫和细胞免疫反应。利用聚合酶链反应(PCR)扩增,我们研究了从一名ALL患者获得的重链可变区基因,以及它们是否能在DBA/2小鼠中诱导体液免疫和细胞免疫反应。将VH序列克隆到用于皮内DNA疫苗接种的哺乳动物表达载体中,并克隆到细菌表达载体中以获得用于蛋白质印迹分析的VH蛋白。将编码VH基因的哺乳动物表达载体以7天的间隔给小鼠注射3次,并将其转导到P1HTR(DBA/2的同基因肿瘤)中,作为检测细胞免疫的靶细胞。接种小鼠的脾细胞对靶细胞表现出显著的细胞毒性T淋巴细胞反应。通过蛋白质印迹分析,我们还能在所有小鼠血清中检测到微量的抗VH抗体。这种通过皮内注射诱导细胞免疫的方法简便且具有可变区特异性,可在B细胞恶性肿瘤化疗后用作疫苗。

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