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.

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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. The percentage of hapten-augmentable PFC present in mice during the primary response to trinitrophenylated Ficoll (TNP-F) increases with age. Apparently there is a relative increase in the auto-anti-idiotypic antibody response with age and therefore a greater antibody production down-regulation. The effect of age on idiotype expression was also studied. Hapten-reversible plaque formation inhibition was used as an assay for anti-idiotype antibody and idiotype-bearing antibody-secreting cells. Sera from aged (21-22 mo. 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. These sera inhibited plaque formation by cells from only 50% of similarly immunized young adult (6-8 wk old) mice and 20% of immature (3-4 wk old) syngeneic mice. Sera from TNP-F-immunized young adult or immature mice inhibited plaque formation 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. Apparently the repertoire of TNP-specific idiotypes that are produced in response to TNP-F varies with age in syngeneic mice.