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The proposal made in 1970-1974 (8(~89) was that the given VLVHpairs wereselected for the specificities of unique survival value that they encoded, and the ’germline" (STAGEI or high copy number) encoded repertoire resulted from random complementation of these V-gene segments. The selection by carbohydrates on pathogens and by autogenously generated macromolecularwaste ("housekeeping" antigens) was justified later (65), by arguing that these substances vary slowly enough to be tracked by the mammaliangenome.

The two choices were: ~v tolerance 1) i ~[2~ductio cell n or " 2) i-cell ~ induction Annual Reviews Annu. Rev. Immunol. 12:1-62. org by HINARI on 08/30/07. For personal use only. e. recognition of the carrier is required for induction, not unresponsiveness). Later the second choice was rejected on the a priori grounds (49, 51) that suppression cannot regulate the S/NSdiscrimination. If I maybe permitted a reflection, all too often a dominant, albeit correct, idea narrows one’s horizons, shutting out the ability to place an observation rejected in that frameworkinto another framework where it is uniquely illuminating.

However, the statement, "All of the specificities expressed by the individual are encoded in the germline," is an assumption,not a theory. To makeit a theory, the selection pressures that maintain the germline must be considered, and this requires an understanding of the relationship between recognition (the repertoire) and an effective effector function. This same commentapplies to all of the Annual Reviews Annu. Rev. Immunol. 12:1-62. org by HINARI on 08/30/07. For personal use only. ON THINKING AND WISDOM 47 "big bang" theories of GOD(see p.

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Annual Review of Immunology Volume 12 1994 by Annual Reviews


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