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针对B细胞淋巴瘤的独特型DNA疫苗。

Idiotypic DNA vaccines against B-cell lymphoma.

作者信息

Stevenson F K, Zhu D, King C A, Ashworth L J, Kumar S, Hawkins R E

机构信息

Tenovus Laboratory, Southampton University Hospitals, UK.

出版信息

Immunol Rev. 1995 Jun;145:211-28. doi: 10.1111/j.1600-065x.1995.tb00083.x.

Abstract

Idiotypic antigens are clearly defined tumor-associated protein antigens, which can induce protective immunity against lymphoma. Because each patient requires an individual vaccine, idiotypic antigens also provide ideal candidates for exploring the feasibility of replacing protein antigens by DNA vaccines. Component idiotypic variable region genes can be identified in patients' tumor biopsies and rapidly assembled as scFv sequences. These can be used to produce recombinant scFv protein in bacteria, or as direct naked DNA vaccines. A preliminary small trial of DNA vaccines for chemotherapy-resistant patients with lymphoma has begun. Intramuscular idiotypic DNA vaccination in a mouse model induces low levels of anti-idiotypic antibody in serum. Levels can be increased dramatically by coinjection of DNA plasmids encoding either IL-2 or GM-CSF, and specific proliferative anti-idiotypic T cells are induced. However protective immunity remains to be demonstrated, and a possible reason for this may lie in the continued secretion of idiotypic scFv antigen which blocks antibody activity by formation of immune complexes. Methods for regulating secretion of antigen are required before this category of tumor antigen can be fully exploited as a vaccine. The power of DNA technology should allow analysis and manipulation of pathways of antigen presentation to induce maximal therapeutic attack on neoplastic B cells. In addition, lymphoma presents a model for application of DNA technology to the wide range of human tumors known to harbor potential tumor antigens.

摘要

独特型抗原是明确界定的肿瘤相关蛋白抗原,可诱导针对淋巴瘤的保护性免疫。由于每个患者都需要个体化疫苗,独特型抗原也为探索用DNA疫苗替代蛋白抗原的可行性提供了理想的候选物。可在患者的肿瘤活检组织中鉴定出组成独特型可变区基因,并迅速组装成单链抗体(scFv)序列。这些可用于在细菌中生产重组scFv蛋白,或用作直接的裸DNA疫苗。针对化疗耐药的淋巴瘤患者的DNA疫苗初步小型试验已经开始。在小鼠模型中进行肌内独特型DNA疫苗接种可诱导血清中低水平的抗独特型抗体。通过共注射编码IL-2或GM-CSF的DNA质粒,水平可显著提高,并诱导出特异性增殖的抗独特型T细胞。然而,保护性免疫仍有待证实,其可能的原因可能在于独特型scFv抗原的持续分泌,该抗原通过形成免疫复合物来阻断抗体活性。在这类肿瘤抗原能够作为疫苗被充分利用之前,需要调节抗原分泌的方法。DNA技术的强大功能应能分析和操纵抗原呈递途径,以诱导对肿瘤性B细胞的最大治疗性攻击。此外,淋巴瘤为将DNA技术应用于已知含有潜在肿瘤抗原的广泛人类肿瘤提供了一个模型。

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