Somatic hypermutation in peritoneal B1b cells

Molecular Immunology

Volumn 46, Issue 8-9, 2009, Pages 1613-1619

  Roy, Bishnudeo ^a   Shukla, Swati ^a   Łyszkiewicz, Marcin ^a   Krey, Martina ^a   Viegas, Nuno ^a   Düber, Sandra ^a   Weiss, Siegfried ^a  

^a HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

Author keywords

Antibodies; B cell subpopulations; B cells; Isotype switch; Lipopolysaccharide

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN M; LIPOPOLYSACCHARIDE;

ANIMAL CELL; ARTICLE; B LYMPHOCYTE; B LYMPHOCYTE ACTIVATION; CONTROLLED STUDY; ENZYME LINKED IMMUNOSPOT ASSAY; IMMUNOGLOBULIN PRODUCTION; LYMPHOCYTE SUBPOPULATION; MOUSE; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PERITONEUM CELL; PRIORITY JOURNAL; SOMATIC HYPERMUTATION;

ANIMALS; B-LYMPHOCYTES; BASE SEQUENCE; IMMUNOGLOBULIN A; IMMUNOGLOBULIN VARIABLE REGION; LIPOPOLYSACCHARIDES; LYMPHOCYTE ACTIVATION; MICE; MICE, INBRED BALB C; MOLECULAR SEQUENCE DATA; MUTATION; PERITONEAL CAVITY; PERITONEUM; SEQUENCE HOMOLOGY, NUCLEIC ACID; SOMATIC HYPERMUTATION, IMMUNOGLOBULIN;

MURINAE; MUS;

EID: 64149127591     PISSN: 01615890     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molimm.2009.02.026     Document Type: Article

References (31)

1. Alugupalli K.R., Leong J.M., Woodland R.T., Muramatsu M., Honjo T., and Gerstein R.M. B1b lymphocytes confer T cell-independent long-lasting immunity. Immunity 21 (2004) 379-390
2. Baumgarth N., Tung J.W., and Herzenberg L.A. Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion. Springer Semin. Immunopathol. 26 (2005) 347-362
3. Berland R., and Wortis H.H. Origins and functions of B-1 cells with notes on the role of CD5. Annu. Rev. Immunol. 20 (2002) 253-300
4. Bos N.A., Bun J.C., Popma S.H., Cebra E.R., Deenen G.J., van der Cammen M.J., Kroese F.G., and Cebra J.J. 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. Infect. Immun. 64 (1996) 616-623
5. de Waard R., Dammers P.M., Tung J.W., Kantor A.B., Wilshire J.A., Bos N.A., Herzenberg L.A., and Kroese F.G. Presence of germline and full-length IgA RNA transcripts among peritoneal B-1 cells. Dev. Immunol. 6 (1998) 81-87
6. Fagarasan S., Shinkura R., Kamata T., Nogaki F., Ikuta K., Tashiro K., and Honjo T. Alymphoplasia (aly)-type nuclear factor kappaB-inducing kinase (NIK) causes defects in secondary lymphoid tissue chemokine receptor signaling and homing of peritoneal cells to the gut-associated lymphatic tissue system. J. Exp. Med. 191 (2000) 1477-1486
7. Geiger K.D., Klein U., Brauninger A., Berger S., Leder K., Rajewsky K., Hansmann M.L., and Kuppers R. CD5-positive B cells in healthy elderly humans are a polyclonal B cell population. Eur. J. Immunol. 30 (2000) 2918-2923
8. Haas K.M., Poe J.C., Steeber D.A., and Tedder T.F. B-1a and B-1b cells exhibit distinct developmental requirements and have unique functional roles in innate and adaptive immunity to S. pneumoniae. Immunity 23 (2005) 7-18
9. Hastings W.D., Tumang J.R., Behrens T.W., and Rothstein T.L. Peritoneal B-2 cells comprise a distinct B-2 cell population with B-1b-like characteristics. Eur. J. Immunol. 36 (2006) 1114-1123
10. Hayakawa K., and Hardy R.R. Development and function of B-1 cells. Curr. Opin. Immunol. 12 (2000) 346-353
11. Hayakawa K., Hardy R.R., Honda M., Herzenberg L.A., Steinberg A.D., and Herzenberg L.A. Ly-1 B cells: functionally distinct lymphocytes that secrete IgM autoantibodies. Proc. Natl. Acad. Sci. U.S.A. 81 (1984) 2494-2498
12. Herzenberg L.A., and Herzenberg L.A. Toward a layered immune system. Cell 59 (1989) 953-954
13. Herzenberg L.A., Kantor A.B., and Herzenberg L.A. Layered evolution in the immune system: a model for the ontogeny and development of multiple lymphocyte lineages. Ann. N.Y. Acad. Sci. 651 (1992) 1-9
14. Kaminski D.A., and Stavnezer J. Enhanced IgA class switching in marginal zone and B1 B cells relative to follicular/B2 B cells. J. Immunol. 177 (2006) 6025-6029
15. Kantor A.B., and Herzenberg L.A. Origin of murine B cell lineages. Annu. Rev. Immunol. 11 (1993) 501-538
16. Kosco-Vilbois M.H., Bonnefoy J.Y., and Chvatchko Y. The physiology of murine germinal center reactions. Immunol. Rev. 156 (1997) 127-136
17. Kroese F.G., Butcher E.C., Stall A.M., Lalor P.A., Adams S., and Herzenberg L.A. Many of the IgA producing plasma cells in murine gut are derived from self-replenishing precursors in the peritoneal cavity. Int. Immunol. 1 (1989) 75-84
18. Liu Y.J., Malisan F., de Bouteiller O., Guret C., Lebecque S., Banchereau J., Mills F.C., Max E.E., and Martinez-Valdez H. Within germinal centers, isotype switching of immunoglobulin genes occurs after the onset of somatic mutation. Immunity 4 (1996) 241-250
19. Macpherson A.J., Gatto D., Sainsbury E., Harriman G.R., Hengartner H., and Zinkernagel R.M. A primitive T cell-independent mechanism of intestinal mucosal IgA responses to commensal bacteria. Science 288 (2000) 2222-2226
20. Martin F., Oliver A.M., and Kearney J.F. Marginal zone and B1 B cells unite in the early response against T-independent blood-borne particulate antigens. Immunity 14 (2001) 617-629
21. McHeyzer-Williams L.J., Driver D.J., and McHeyzer-Williams M.G. Germinal center reaction. Curr. Opin. Hematol. 8 (2001) 52-59
22. Montecino-Rodriguez E., Leathers H., and Dorshkind K. Identification of a B-1 B cell-specified progenitor. Nat. Immunol. 7 (2006) 293-301
23. Neuberger M.S., and Milstein C. Somatic hypermutation. Curr. Opin. Immunol. 7 (1995) 248-254
24. Ochsenbein A.F., Fehr T., Lutz C., Suter M., Brombacher F., Hengartner H., and Zinkernagel R.M. Control of early viral and bacterial distribution and disease by natural antibodies. Science 286 (1999) 2156-2159
25. Peters A., and Storb U. Somatic hypermutation of immunoglobulin genes is linked to transcription initiation. Immunity 4 (1996) 57-65
26. Stall A.M., Adams S., Herzenberg L.A., and Kantor A.B. Characteristics and development of the murine B-1b (Ly-1 B sister) cell population. Ann. N.Y. Acad. Sci. 651 (1992) 33-43
27. Stall A.M., Wells S.M., and Lam K.P. B-1 cells: unique origins and functions. Semin. Immunol. 8 (1996) 45-59
28. Stoel M., Jiang H.Q., van Diemen C.C., Bun J.C., Dammers P.M., Thurnheer M.C., Kroese F.G., Cebra J.J., and Bos N.A. Restricted IgA repertoire in both B-1 and B-2 cell-derived gut plasmablasts. J. Immunol. 174 (2005) 1046-1054
29. Tarlinton D. Germinal centers: form and function. Curr. Opin. Immunol. 10 (1998) 245-251
30. Tempest P.R., White P., Buttle M., Carr F.J., and Harris W.J. Identification of framework residues required to restore antigen binding during reshaping of a monoclonal antibody against the glycoprotein gB of human cytomegalovirus. Int. J. Biol. Macromol. 17 (1995) 37-42
31. Tumang J.R., Frances R., Yeo S.G., and Rothstein T.L. Spontaneously Ig-secreting B-1 cells violate the accepted paradigm for expression of differentiation-associated transcription factors. J. Immunol. 174 (2005) 3173-3177