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Updated: Sep 28, 2026

T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing
Published on: January 12, 2021
If the immune repertoire evolved to be large, random, and somatically generated, then
Rodney E Langman1, Melvin Cohn
1Conceptual Immunology Group, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Abstract:
The evolution of the somatically generated random combining site repertoire of the "adaptive" immune system depended on the concurrent appearance of a somatic process that sorted the repertoire into anti-self and anti-nonself. Unlike the germline-selected sorting process characteristic of "innate" defense mechanisms, somatic sorting of the repertoire requires that antigens be classified based on their behavior, not on their physical or chemical properties. As specific recognitive combining sites (paratopes) define antigenic determinants (epitopes), the sorting of the repertoire operates epitope-by-epitope. By contrast, the coupling of the paratope to effector function must operate antigen-by-antigen because the response to each epitope on the antigen must be in the same effector class (i.e., coherent). This distinction resolves a long standing debate and provides a basis for analyzing the various models.
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