How adaptive antibodies facilitate the evolution of natural antibodies

It is shown how Ig specificities, randomly generated in conventional B cells, come to be expressed in the genetically‐determinate B1 population. Thus the adaptive antibody population facilitates the evolution of the natural antibody repertoire, in accordance with the Baldwin effect in the evolution of instinct. The evolution of these two populations is discussed under both the‘proximal usage’and‘preferential expression’hypotheses of biased Ig gene segment usage. This process is independent of theories of B1 function.

[1]  J. Baldwin A New Factor in Evolution , 1896, The American Naturalist.

[2]  H. Osborn OYTOGENIC AND PHYLOGENIC VARIATION. , 1896, Science.

[3]  C L Morgan,et al.  ON MODIFICATION AND VARIATION. , 1896, Science.

[4]  C. Waddington Canalization of Development and the Inheritance of Acquired Characters , 1942, Nature.

[5]  G. Simpson THE BALDWIN EFFECT , 1953 .

[6]  L. Hood,et al.  Amino acid sequence of homogeneous antibodies to dextran and DNA rearrangments in heavy chain V-region gene segments , 1980, Nature.

[7]  F. Alt,et al.  Preferential utilization of the most JH-proximal VH gene segments in pre-B-cell lines , 1984, Nature.

[8]  R. Dildrop,et al.  VH‐gene expression in murine lipopolysaccharide blasts distributes over the nine known VH‐gene groups and may be random , 1985, European journal of immunology.

[9]  O. Vainio,et al.  Immunoglobulin‐bearing stem cells for clones of B (bursa‐derived) lymphocytes , 1985, European journal of immunology.

[10]  R. Hardy,et al.  Immunoglobulin‐bearing B cells reconstitute and maintain the murine Ly‐1 B cell lineage , 1986, European journal of immunology.

[11]  L. Herzenberg,et al.  The Ly-1 B cell lineage. , 1986, Immunological reviews.

[12]  L. Herzenberg,et al.  The LY‐1B Cell Lineage , 1986 .

[13]  John Maynard Smith,et al.  When learning guides evolution , 1987, Nature.

[14]  K. Rajewsky,et al.  Expansion and functional activity of Ly‐1+ B cells upon transfer of peritoneal cells into allotype‐congenic, newborn mice , 1987, European journal of immunology.

[15]  J. Weill,et al.  The chicken B cell compartment. , 1987, Science.

[16]  Geoffrey E. Hinton,et al.  How Learning Can Guide Evolution , 1996, Complex Syst..

[17]  J. Teale,et al.  Comparison of the fetal and adult functional B cell repertoires by analysis of VH gene family expression , 1988, The Journal of experimental medicine.

[18]  R. Hardy,et al.  Normal, autoimmune, and malignant CD5+ B cells: the Ly-1 B lineage? , 1988, Annual review of immunology.

[19]  K. Rajewsky,et al.  Germline antibody V regions as determinants of clonal persistence and malignant growth in the B cell compartment. , 1988, The EMBO journal.

[20]  W. Wcislo BEHAVIORAL ENVIRONMENTS AND EVOLUTIONARY CHANGE , 1989 .

[21]  S. Clarke,et al.  Biased immunoglobulin variable region gene expression by Ly‐1 B cells due to clonal selection , 1989, European journal of immunology.

[22]  S. Clarke,et al.  Organization and expression of vh gene families preferentially expressed by ly‐1+ (cd5) b cells , 1989, European journal of immunology.

[23]  R. Riblet,et al.  Conservation of an immunoglobulin variable-region gene family indicates a specific, noncoding function. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[24]  C. Kocks,et al.  Stable expression and somatic hypermutation of antibody V regions in B-cell developmental pathways. , 1989, Annual review of immunology.

[25]  E. Sasso,et al.  Human IgM molecules that bind staphylococcal protein A contain VHIII H chains. , 1989, Journal of immunology.

[26]  J. Teale,et al.  VH gene family repertoire of resting B cells. Preferential use of D-proximal families early in development may be due to distinct B cell subsets. , 1989, Journal of immunology.

[27]  R. Perlmutter,et al.  Structure and evolution of mammalian VH families. , 1990, International immunology.

[28]  F. Alt,et al.  Biased expression of JH-proximal VH genes occurs in the newly generated repertoire of neonatal and adult mice , 1990, The Journal of experimental medicine.

[29]  J. Teale,et al.  Contribution of the CD5+ B cell to D-proximal VH family expression early in ontogeny. , 1990, Journal of immunology.

[30]  G. Morahan,et al.  The peritoneal Ly‐1 (CD5) B cell repertoire is unique among murine B cell repertoires , 1990, European journal of immunology.

[31]  K. Rajewsky,et al.  Most peripheral B cells in mice are ligand selected , 1991, The Journal of experimental medicine.

[32]  K. Meek,et al.  Conservation of the most JH proximal Ig VH gene segment (VHVI) throughout primate evolution. , 1991, Journal of immunology.

[33]  A. Coutinho,et al.  Biased VH gene expression in murine CD5 B cells results from age‐dependent cellular selection , 1991, European journal of immunology.

[34]  T. Logtenberg,et al.  Antibody specificity and immunoglobulin VH utilization of human monoclonal CD5+ B cell lines , 1991, European journal of immunology.

[35]  A. Kantor,et al.  Layered Evolution in the Immune System , 1992 .

[36]  F. Kroese,et al.  The evolution of immune memory and germinal centers. , 1992, Immunology today.

[37]  Deletion mapping of Ig VH gene segments expressed in human CD5 B cell lines. JH proximity is not the sole determinant of the restricted fetal VH gene repertoire. , 1992, Journal of immunology.

[38]  P. Ernst,et al.  Enhancement of mucosal antibody responses to Salmonella typhimurium and the microbial hapten phosphorylcholine in mice with X-linked immunodeficiency by B-cell precursors from the peritoneal cavity , 1992, Infection and immunity.

[39]  J. Kearney,et al.  The Fetal Omentum in Mice and Humans , 1992, Annals of the New York Academy of Sciences.

[40]  K. Knight,et al.  Restricted VH gene usage and generation of antibody diversity in rabbit. , 1992, Annual review of immunology.

[41]  D. Schatz,et al.  Human anti-pneumococcal polysaccharide antibodies are secreted by the CD5- B cell lineage. , 1992, Cellular immunology.

[42]  C. Raman,et al.  CD5+ B cells predominate in peripheral tissues of rabbit. , 1992, Journal of immunology.

[43]  J. Marchalonis,et al.  Antibody production in sharks and humans: a role for natural antibodies. , 1993, Developmental and comparative immunology.

[44]  J. V. Es,et al.  Expression pattern of the most JH-proximal human VH gene segment (VH6) in the B cell and antibody repertoire suggests a role of VH6-encoded IgM antibodies in early ontogeny. , 1993, Journal of immunology.

[45]  L. Herzenberg,et al.  B-cell lineages exist in the mouse. , 1993, Immunology today.

[46]  J. Travis Tracing the immune system's evolutionary history. , 1993, Science.

[47]  V. Pascual,et al.  Analysis of Ig H chain gene segment utilization in human fetal liver. Revisiting the "proximal utilization hypothesis". , 1993, Journal of immunology.

[48]  S. Clarke,et al.  Development of B-1 cells: segregation of phosphatidyl choline-specific B cells to the B-1 population occurs after immunoglobulin gene expression , 1994, The Journal of experimental medicine.

[49]  E. Cooper,et al.  Primordial Immunity: Foundations for the Vertebrate Immune System , 1994 .

[50]  J. Marchalonis,et al.  Development of an Immune System a , 1994, Annals of the New York Academy of Sciences.

[51]  R. Anderson,et al.  Learning and evolution: a quantitative genetics approach. , 1995, Journal of theoretical biology.