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By Frank J. Dixon (Ed.)

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Froscher, K. Marcu, and N. R. Klinman, unpublished observations). Although these studies are preliminary and must be extended to other murine strains, it appears that V, genes other than the Vh S107 can indeed give rise to bona fide Type I PC-specific antibodies. However, in young mice of all tested strains, these V region combinations are not expressed within the normal B cell repertoire. The reasons for the late expression of anti-PC antibodies utilizing non-S107 V, gene segments is currently the subject of intensive investigation.

As can be seen in Table 11, the frequency with which these cells occur in the sIg- bone marrow pool of BALB/c mice falls within the normalization range, and, thus, like B cells responsive to PC, the high frequency of A-DEX B cells in the splenic B cell population of BALB/c mice appears to be the result of a high frequency of their recurrence within the sIg- precursor population. , 1985). In the fragment culture system, responses with these characteristics are maximized by stimulation with protein conjugates of analogs of NP such as NNP and (4-hydroxy-5-iodo-3-nitrophenyl) acetyl (NIP) (Stashenko and Klinman, 1980; Riley and Klinman, 1986).

6 " Zharhary and Klinman (1983). Riley and Klinman (1985). Riley and Klinman (1986). Klinman and Stone (1983). Froscher and Klinman (1985). 'Riley e t al. (1983). Froscher and Klinman (1986). Morrow et al. (1987). B cells responsive to most antigenic determinants is determined by the frequency with which B cells of these specificities have emerged from the developing bone marrow progenitor pool and appears to be influenced little, if at all, by the environmental milieu of the developing B cells.

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