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正常免疫反应过程中自身抗独特型抗体的产生:与衰老相关的自身抗独特型抗体反应及独特型库的变化。

Production of auto-anti-idiotypic antibody during the normal immune response: changes in the auto-anti-idiotypic antibody response and the idiotype repertoire associated with aging.

作者信息

Goidl E A, Thorbecke G J, Weksler M E, Siskind G W

出版信息

Proc Natl Acad Sci U S A. 1980 Nov;77(11):6788-92. doi: 10.1073/pnas.77.11.6788.

Abstract

Hapten-augmentable plaque-forming cells (PFC) are cells whose secretion of antibody is specifically inhibited by surface-bound auto-anti-iodotype antibody that can be displaced by hapten. This study showed that the percentage of hapten-augmentable PFC present in mice during the primary response to trinitrophenylated Ficoll (TNP-F) increases with age. The data suggest that there is a relative increase in the auto-anti-idiotypic antibody response with age and therefore a greater down-regulation of antibody production. The effect of age on idiotype expression was also studied. Hapten-reversible inhibition of plaque formation was used as an assay for anti-inhibition of plaque formation was used as an assay for anti-idiotype antibody and idiotype-bearing antibody-secreting cells. Sera from aged (21- to 22-month-old) C57BL/6 mice immunized with TNP-F significantly inhibited plaque formation, in a hapten-reversible manner, by spleen cells from 81% of TNP-F-immunized aged mice. However, these sera inhibited plaque formation by cells from only 50% of similarly immunized young adult (6- to 8-week-old) mice and 20% of immature (3- to 4-week-old) syngeneic mice. Similarly, sera from TNP-F-immunized young adult or immature mice inhibited formation of plaques by cells from immunized donors of the same age as the mice from whom the serum was obtained, but only rarely inhibited plaque formation by cells from mice of other age groups. The data thus suggest that the repertoire of TNP-specific idiotypes that are produced in response to TNP-F varies with age in syngeneic mice.

摘要

半抗原增强性斑块形成细胞(PFC)是其抗体分泌受到表面结合的自身抗独特型抗体特异性抑制的细胞,该抗体可被半抗原取代。本研究表明,在对三硝基苯基化菲可(TNP-F)的初次应答期间,小鼠体内存在的半抗原增强性PFC百分比随年龄增加。数据表明,自身抗独特型抗体应答随年龄相对增加,因此抗体产生的下调作用更强。还研究了年龄对独特型表达的影响。半抗原可逆性抑制斑块形成被用作抗独特型抗体和携带独特型抗体分泌细胞的检测方法。用TNP-F免疫的老年(21至22月龄)C57BL/6小鼠的血清,以半抗原可逆的方式,显著抑制了81%的TNP-F免疫老年小鼠脾脏细胞形成斑块。然而,这些血清仅抑制了50%的类似免疫的年轻成年(6至8周龄)小鼠和20%的同基因未成熟(3至4周龄)小鼠的细胞形成斑块。同样,用TNP-F免疫的年轻成年或未成熟小鼠的血清,抑制了与提供血清的小鼠年龄相同的免疫供体的细胞形成斑块,但很少抑制其他年龄组小鼠的细胞形成斑块。因此,数据表明,在同基因小鼠中,针对TNP-F产生的TNP特异性独特型库随年龄而变化。

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