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通过向新生BALB/c小鼠给予抗MOPC 315 IgA单克隆抗独特型抗体来保护成年BALB/c小鼠免受MOPC 315骨髓瘤侵害。

Protection of adult BALB/c mice against MOPC 315 myeloma by neonatal administration of monoclonal anti-idiotypic antibody to MOPC 315 IgA.

作者信息

Gorczynski R, Baumal R, Boulanger M, Marks A

出版信息

J Natl Cancer Inst. 1986 Sep;77(3):801-7. doi: 10.1093/jnci/77.3.801.

Abstract

Ascitic fluid containing monoclonal anti-idiotypic antibody (AIA) to MOPC 315 IgA was administered to newborn BALB/c mice, and the mice were challenged in adulthood with IgA-producing MOPC 315 myeloma cells. Administration of AIA D10 (a hybrid molecule containing IgG1 and IgG2a heavy chains), G3 (IgG2b), and A2 (IgG1), all of which reacted with MOPC 315 cells in a cell-binding radioimmunoassay, prolonged survival and reduced the percentage of IgA-producing spleen fragments derived from mice challenged with MOPC 315 myeloma cells, but not with cells of a related IgA-producing myeloma, MOPC 460. Reduction in the percentage of IgA-producing spleen fragments was prevented by treatment of spleen cells prior to culture with anti-Thy 1.2 antibody and complement. Administration of AIA F1 (IgG2a), which did not react with MOPC 315 cells in vitro, or of an antibody with no AIA activity did not produce a similar protection. These results suggest that administration of AIA to MOPC 315 IgA to neonatal BALB/c mice induces idiotype-specific T-lymphocytes that protect these mice against a challenge with MOPC 315 myeloma cells in adulthood.

摘要

将含有针对MOPC 315 IgA的单克隆抗独特型抗体(AIA)的腹水注射给新生BALB/c小鼠,然后在成年期用产生IgA的MOPC 315骨髓瘤细胞对这些小鼠进行攻击。在细胞结合放射免疫分析中与MOPC 315细胞发生反应的AIA D10(一种含有IgG1和IgG2a重链的杂合分子)、G3(IgG2b)和A2(IgG1)的注射延长了生存期,并降低了来自用MOPC 315骨髓瘤细胞攻击的小鼠的产生IgA的脾片段的百分比,但对相关的产生IgA的骨髓瘤MOPC 460细胞攻击的小鼠则没有这种作用。在用抗Thy 1.2抗体和补体培养之前对脾细胞进行处理,可防止产生IgA的脾片段百分比的降低。在体外不与MOPC 315细胞发生反应的AIA F1(IgG2a)或没有AIA活性的抗体的注射不会产生类似的保护作用。这些结果表明,给新生BALB/c小鼠注射针对MOPC 315 IgA的AIA可诱导独特型特异性T淋巴细胞,这些T淋巴细胞可保护这些小鼠在成年期免受MOPC 315骨髓瘤细胞的攻击。

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