Literature DB >> 16139887

What are the commonalities governing the behavior of humoral immune recognitive repertoires?

Melvin Cohn1.   

Abstract

The humoral repertoire of immune systems is large, random and somatically selected. It is derived from a germline selected repertoire by a variety of diversification mechanisms, complementation of subunits, mutation and gene conversion. However derived, the end-product must be able to recognize and rid a vast variety of pathogens. This is accomplished by viewing antigens as combinatorials of epitopes, an astuce that permits a small repertoire to respond sufficiently rapidly to a vast antigenic universe. A somatically generated repertoire, however, requires a solution to two problems. First, a somatic mechanism for a self-nonself discrimination has to be put in place. Second, the repertoire has to be coupled to the effector mechanisms in a coherent fashion. The rules governing these two mechanisms are species-independent and delineate the parameters of all immune repertoires, whatever the somatic mechanism used to generate them.

Mesh:

Year:  2006        PMID: 16139887     DOI: 10.1016/j.dci.2005.06.015

Source DB:  PubMed          Journal:  Dev Comp Immunol        ISSN: 0145-305X            Impact factor:   3.636


  10 in total

Review 1.  A commentary on the Zinkernagel-Hengartner 'Credo 2004'.

Authors:  M Cohn
Journal:  Scand J Immunol       Date:  2005-06       Impact factor: 3.487

Review 2.  Does the signal for the activation of T cells originate from the antigen-presenting cell or the effector T-helper?

Authors:  Melvin Cohn
Journal:  Cell Immunol       Date:  2006-09-11       Impact factor: 4.868

Review 3.  The Tritope Model for restrictive recognition of antigen by T-cells II. Implications for ontogeny, evolution and physiology.

Authors:  Melvin Cohn
Journal:  Mol Immunol       Date:  2007-09-21       Impact factor: 4.407

Review 4.  An in depth analysis of the concept of "polyspecificity" assumed to characterize TCR/BCR recognition.

Authors:  Melvin Cohn
Journal:  Immunol Res       Date:  2008       Impact factor: 2.829

5.  Analysis of Paris meeting redefining the "self" of the immune system.

Authors:  Melvin Cohn
Journal:  Immunol Res       Date:  2015-05       Impact factor: 2.829

Review 6.  Signaling interactions predicted by the Tritope model of the TCR.

Authors:  Melvin Cohn
Journal:  Immunol Res       Date:  2017-10       Impact factor: 2.829

7.  On the logic of restrictive recognition of peptide by the T-cell antigen receptor.

Authors:  Melvin Cohn
Journal:  Immunol Res       Date:  2011-05       Impact factor: 2.829

8.  A rationalized set of default postulates that permit a coherent description of the immune system amenable to computer modeling.

Authors:  M Cohn
Journal:  Scand J Immunol       Date:  2008-10       Impact factor: 3.487

9.  A hypothesis accounting for the paradoxical expression of the D gene segment in the BCR and the TCR.

Authors:  Melvin Cohn
Journal:  Eur J Immunol       Date:  2008-07       Impact factor: 5.532

10.  Antibody binding loop insertions as diversity elements.

Authors:  Csaba Kiss; Hugh Fisher; Emanuele Pesavento; Minghua Dai; Rosa Valero; Milan Ovecka; Rhiannon Nolan; M Lisa Phipps; Nileena Velappan; Leslie Chasteen; Jennifer S Martinez; Geoffrey S Waldo; Peter Pavlik; Andrew R M Bradbury
Journal:  Nucleic Acids Res       Date:  2006-10-05       Impact factor: 16.971

  10 in total

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