Sequence analysis of human IgVH genes indicates that ileal lamina propria plasma cells are derived from Peyer's patches

The origin of human ileal lamina propria (LP) plasma cells has been investigated using a technique based on microdissection of cells from immunohistochemically stained tissue sections. We have sequenced rearranged IgVH4.21, IgVH 5 family and IgVH6 genes from Peyer's patch germinal center (GC) cells and plasma cells from the ileal LP. Clonally related cells were identified by comparison of their complementarity determining region (CDR) 3 sequences and patterns of somatic mutation. We observed Ig genes from B cells in the GC of Peyer's patches which were related to Ig genes from plasma cells in the ileal LP, demonstrating that clonally related cells span these sites. In addition, groups of clonally related, but diversified plasma cells were common in the lamina propria. All Ig genes isolated from LP plasma cells were heavily mutated. The distribution of mutations in the CDR of the Ig heavy chain variable region (VH) genes which were considered to be the expressed alleles in LP plasma cells was consistent with an affinity‐matured response. These observations provide compelling evidence for the origin of human ileal plasma cells from the Peyer's patches.

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

[2]  L. Arnold,et al.  Normal mouse peritoneum contains a large population of Ly-1+ (CD5) B cells that recognize phosphatidyl choline. Relationship to cells that secrete hemolytic antibody specific for autologous erythrocytes , 1988, The Journal of experimental medicine.

[3]  J. Tseng Transfer of lymphocytes of Peyer's patches between immunoglobulin allotype congenic mice: repopulation of the IgA plasma cells in the gut lamina propria. , 1981, Journal of immunology.

[4]  C. Bona,et al.  Germline V genes encode viable motheaten mouse autoantibodies against thymocytes and red blood cells. , 1990, Journal of immunology.

[5]  P. Isaacson,et al.  Analysis of mutations in immunoglobulin heavy chain variable region genes of microdissected marginal zone (MGZ) B cells suggests that the MGZ of human spleen is a reservoir of memory B cells , 1995, The Journal of experimental medicine.

[6]  P. Ogra Handbook of mucosal immunology , 1994 .

[7]  P. Casali,et al.  The CDR1 sequences of a major proportion of human germline Ig VH genes are inherently susceptible to amino acid replacement. , 1994, Immunology today.

[8]  A S Perelson,et al.  Cyclic re-entry of germinal center B cells and the efficiency of affinity maturation. , 1993, Immunology today.

[9]  S. Shinton,et al.  A single VH gene is utilized predominantly in anti-BrMRBC hybridomas derived from purified Ly-1 B cells. Definition of the VH11 family. , 1989, Journal of immunology.

[10]  L. Herzenberg,et al.  18 – The Role of B-1 Cells in Mucosal Immune Responses , 1994 .

[11]  C. Milstein,et al.  Analysis of somatic hypermutation in mouse Peyer's patches using immunoglobulin kappa light-chain transgenes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[12]  I. Turesson Distribution of immunoglobulin-containing cells in human bone marrow and lymphoid tissues. , 2009, Acta medica Scandinavica.

[13]  F. Kroese,et al.  Monoclonal immunoglobulin A derived from peritoneal B cells is encoded by both germ line and somatically mutated VH genes and is reactive with commensal bacteria , 1996, Infection and immunity.

[14]  P. Krajči,et al.  Immunobiology and immunopathology of human gut mucosa: humoral immunity and intraepithelial lymphocytes. , 1989, Gastroenterology.

[15]  J. D. Capra,et al.  Analysis of somatic mutation in five B cell subsets of human tonsil , 1994, The Journal of experimental medicine.

[16]  K. Anders,et al.  Normal human intestinal B lymphocytes. Increased activation compared with peripheral blood. , 1989, The Journal of clinical investigation.

[17]  Konturek Sj Somatostatin and the gastrointestinal secretions. , 1976 .

[18]  F. Kroese,et al.  Evidence that intestinal IgA plasma cells in μ,ϰ transgenic mice are derived from B-1 (Ly-1 B) cells , 1993 .

[19]  P. Lipsky,et al.  Analysis of the expression of CD5 by human B cells and correlation with functional activity. , 1992, Cellular immunology.

[20]  T. Logtenberg,et al.  The majority of human tonsillar CD5+ B cells express somatically mutated Vχ4 genes , 1993 .

[21]  K. Rajewsky,et al.  Variable region gene analysis of B cell subsets derived from a 4-year- old child: somatically mutated memory B cells accumulate in the peripheral blood already at young age , 1994, The Journal of experimental medicine.

[22]  C. Czerkinsky,et al.  Intestinal immune responses in humans. Oral cholera vaccination induces strong intestinal antibody responses and interferon-gamma production and evokes local immunological memory. , 1991, The Journal of clinical investigation.

[23]  I. Tomlinson,et al.  The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops. , 1992, Journal of molecular biology.

[24]  E. Butcher,et al.  Many of the IgA producing plasma cells in murine gut are derived from self-replenishing precursors in the peritoneal cavity. , 1989, International immunology.

[25]  H. Ikematsu,et al.  Complete sequence of the genes encoding the VH and VL regions of low- and high-affinity monoclonal IgM and IgA1 rheumatoid factors produced by CD5+ B cells from a rheumatoid arthritis patient. , 1991, International immunology.

[26]  M. Mcwilliams,et al.  Differentiation pathway of Peyer's patch precursors of IgA plasma cells in the secretory immune system. , 1981, Cellular immunology.

[27]  I. Sanz,et al.  The smaller human VH gene families display remarkably little polymorphism. , 1989, The EMBO journal.

[28]  K. Rajewsky,et al.  Human IgM+IgD+ B cells, the major B cell subset in the peripheral blood, express Vϰ genes with no or little somatic mutation throughout life , 1993, European journal of immunology.

[29]  P. Isaacson,et al.  Location and sequence of rearranged immunoglobulin genes in human thymus , 1995, European journal of immunology.