An Evolutionarily-Conserved Role for Murine Ly-1 B Cells in Protection Against Bacterial Infections

References

• Herzenberg L A, Stall A M, Lalor P A, Sidman C, Moore W A, Parks D R, Herzenberg L A. The Ly‐l B cell lineage. Immunol Rev. 1986; 93: 81–102
   PubMed Web of Science ®Google Scholar
• Marcos M A, Huetz F, Pereira P, Andreu J ‐L, Martinez A C, Coutinho A. Further evidence for coelomic‐associated B lymphocytes. Eur J Immunol. 1989; 19: 2031–2035
   PubMedGoogle Scholar
• Hardy R R, Hayakawa K. Normal, autoimmune, and malignant CD5+ B cells: the Ly‐l B lineage!. Ann Rev Immunol. 1988; 6: 197–218
   PubMed Web of Science ®Google Scholar
• Kipps T J. The CD5 B cell. Adv Immunol. 1989; 47: 117–185
   PubMed Web of Science ®Google Scholar
• Calvert J E, Duggan‐Keen M F, Smith S W G, Givan A L, Bird P. The CD5+ B cell: a B cell lineage with a central role in autoimmune disease?. Autoimmunity. 1988; 1: 223–240
   PubMedGoogle Scholar
• Herzenberg L A, Herzenberg L A. Toward a layered immune system. Cell. 1989; 59: 953–954
   PubMed Web of Science ®Google Scholar
• Lalor P A, Stall A M, Adams S, Herzenberg L A. Permanent alteration of the murine Ly‐1 B repertoire due to selective depletion of Ly‐I B cells in neonatal animals. Eur J Immunol. 1989; 19: 501–506
   Web of Science ®Google Scholar
• Hiernaux J R, Goidl E A, McEvoy S J, Stashak P W, Baker P J, Holmes K L. Characterisation of the immunodeficiency of RIIIS/J mice. Association with the CDS (Ly‐1) B cell lineage. J Immunol. 1989; 142: 1813–1817
   Google Scholar
• Osmond D G. Population dynamics of bone marrow B lymphocytes. Immunol Rev. 1986; 93: 103–124
   PubMed Web of Science ®Google Scholar
• Forster I, Vieira P, Rajewsky K. Flow cytometric analysis of cell proliferation dynamics in the B cell compartment of the mouse. International Immunol. 1989; 1: 322–331
   Google Scholar
• Gray D. Population kinetics of rat peripheral B cells. J Exp Med. 1988; 167: 805–816
   Google Scholar
• MacLennan I C M. Mechanisms of B Cell Neoplasia, F Melchers, M Potter. Roche, Switzerland 1987; 63–73
   Google Scholar
• Lortan J E, Roobottom C A, Oldfield S, MacLennan I C M. Newly produced virgin B cells migrate to secondary lymphoid organs but their capacity to enter follicles is restricted. Eur J Immunol. 1987; 17: 1311–1316
   PubMed Web of Science ®Google Scholar
• Forster I, Rajewsky K. The bulk of the peripheral B cell pool is stable and not rapidly renewed from the bone marrow. Proc Natl Acad Sci USA. 1990; 87: 4781–4784
   PubMedGoogle Scholar
• Solvason N W, Kearney J F. Reconstitution of lymphocyte subsets in Scid mice by transplantation of fetal primordia. Curr Topics Microbiol Immunol. 1989; 152: 161–168
   Google Scholar
• Kroese F G M, Butcher E C, Stall A M, Lalor P A, Adams S, Herzenberg L A. Many of the IgA producing plasma cells in murine gut are derived from self‐replenishing precursors in the peritoneal cavity. International Immunol. 1989; 1: 75–84
   PubMed Web of Science ®Google Scholar
• Hayakawa K, Hardy R R, Stall A M, Herzenberg L A, Herzenberg L A. Immunoglobulin‐bearing B cells reconstitute and maintain the murine Ly‐l B cell lineage. Eur J Immunol. 1986; 16: 1313–1317
   PubMed Web of Science ®Google Scholar
• Lalor P A, Herzenberg L A, Adam S, Stall A M. Feedback regulation of murine Ly‐I B cell development. Eur J Immunol. 1989; 19: 507–513
   Google Scholar
• Hayakawa K, Hardy R R, Herzenberg L A, Herzenberg L A. Progenitors for Ly‐1 B cells are distinct from progenitors for other B cells. J Exp Med. 1985; 161: 1554–1568
   PubMed Web of Science ®Google Scholar
• Forster I, Rajewsky K. Expansion and functional activity of Ly‐l B cells upon transfer of peritoneal cells into allotype‐congenic, newborn mice. Eur J Immunol. 1987; 17: 521–528
   PubMed Web of Science ®Google Scholar
• van der Heijden J, Stok W, Bianchi T J. Contribution of immunoglobulin‐secreting cells in the murine small intestine to the total “background” immunoglobulin production. Immunology. 1987; 62: 551–555
   Web of Science ®Google Scholar
• Kearney J F, Vakil M. Idiotype‐directed interactions during ontogeny play a major role in the establishment of the adult B cell repertoire. Immunol Rev. 1986; 94: 39–50
   PubMed Web of Science ®Google Scholar
• Vakil M, Kearney J F. Functional characterization of monoclonal auto‐anti‐idiotype antibodies isolated from the early B cell repertoire of BALB/c mice. Eur J Immunol. 1986; 16: 1151–1158
   PubMed Web of Science ®Google Scholar
• Vakil M, Sauter H, Paige C, Kearney J F. In vivo suppression of perinatal multispecific B cells results in a distortion of the adult B cell repertoire. Eur J Immunol. 1986; 16: 1159–1165
   PubMedGoogle Scholar
• Masmoudi H, Mota‐Santos T, Huetz F, Couthino A, Cazenave P ‐A. All T15 Id‐positive antibodies (but not the majority of VHT15+ antibodies) are produced by peritoneal CD5+ B lymphocytes. International Immunol. 1990; 2: 516–520
   Google Scholar
• Kearney J F, Barletta R, Quan Z S, Quintans J, Monoclonal V S. heterogenous anti H‐8 antibodies in the analysis of the anti‐phosphorylcholine response in BALB/c mice. Eur J Immunol. 1981; 11: 877–883
   PubMedGoogle Scholar
• Steele E J, Cunningham A J. High proportion of Ig‐producing cells making autoantibodies in normal mice. Nature 1978; 274: 483–484
   PubMed Web of Science ®Google Scholar
• Vieira P, Rajewsky K. The half‐lives of serum immunoglobulins in adult mice. Eur J Immunol. 1988; 18: 313–316
   PubMed Web of Science ®Google Scholar
• Bos N A, Kimura H, Meeuwsen C G, DeVisser H, Harenberg M P, Wostmann B S, Pleasants J R, Benner R, Marcus D M. Serum immunoglobulin levels and naturally occurring antibodies against carbohydrate antigens in germ‐free BALB/c mice fed chemically defined ultrafiltered diet. Eur J Immunol. 1989; 19: 2335–2339
   Google Scholar
• Pereira P, Forni L, Larsson E ‐L, Cooper M, Heusser C, Couthino A. Autonomous activation of B and T cells in antigen‐free mice. Eur J Immunol. 1986; 16: 685–688
   PubMedGoogle Scholar
• Baccala R, Quang T V, Gilbert M, Ternynck T, Avrameas S. Two murine natural polyreactive autoantibodies are encoded by nonmutated germ‐line genes. Proc Natl Acad Sci USA. 1989; 86: 4624–4628
   PubMed Web of Science ®Google Scholar
• Forster I, Gu H, Rajewsky K. Germline antibody V regions as determinants of clonal persistence and malignant growth in the B cell compartment. EMBO J. 1988; 7: 3693–3703
   PubMed Web of Science ®Google Scholar
• Pennell C A, Mercolino T J, Grdina T A, Arnold L W, Haughton G, Clarke S H. Biased immunoglobulin variable region gene expression by Ly‐l B cell due to clonal selection. Eur J immuno1. 1989; 19: 1289–1295
   PubMed Web of Science ®Google Scholar
• Jerne N K. Idiotypic networks and other preconceived ideas. Immunol Rev. 1984; 79: 5–24
   PubMed Web of Science ®Google Scholar
• Lydyard P M, Youinou P Y, Cooke A. CDS‐positive B cells in rheumatoid arthritis and chronic lymphocytic leukemia. Immunol Today. 1987; 8: 37–39
   PubMedGoogle Scholar
• Martinez A C, Pereira P, Toribio M L, Marcos M A, Bandeira A, de la Hera A, Marquez C, Cazenave P ‐A, Couthino A. The participation of B cells and antibodies in the selection and maintenance of T cell repertoires. Immunol Rev. 1988; 101: 191–215
   PubMedGoogle Scholar
• Lundkvist I, Coutinho A, Varela F, Holmberg D. Evidence for a functional idiotypic network among natural antibodies in normal mice. Proc Nail Acad Sci USA. 1989; 86: 5074–5078
   PubMed Web of Science ®Google Scholar
• Nawata Y, Stall A M, Herzenberg L A, Eugui E M, Allison A C. Surface immunoglobulin ligands and cytokines differentially affect proliferation and antibody production by human CD5+ and CD5‐ B lymphocytes. International Immunol. 1990; 2: 603–614
   PubMed Web of Science ®Google Scholar
• Bottomly K. All idiotypes are equal, but some are more equal than others. Immunol Rev. 1984; 79: 45–61
   Google Scholar
• Kocks C, Rajewsky K. Stable expression and somatic hyper‐mutation of antibody V regions in B cell developmental pathways. Ann Rev Immunol. 1989; 7: 537–559
   PubMed Web of Science ®Google Scholar
• Van Snick J, Coulie P. Rheumatoid factors and secondary immune responses in the mouse I. Frequent occurrence of hybridomas secreting IgM anti‐IgG1 autoantibodies after immunization with protein antigens. Eur J Immunol. 1983; 13: 890–894
   PubMed Web of Science ®Google Scholar
• Ternynck T, Avrameas S. Murine natural monoclonal autoantibodies: A study of their polyspecificities and their affinities. Immunol Rev. 1986; 94: 99–112
   PubMed Web of Science ®Google Scholar
• Hayakawa K, Hardy R R, Honda M, Herzenberg L A, Steinberg A D, Herzenberg L A. Ly‐1 B cells: Functionally distinct lymphocytes that secrete IgM autoantibodies. Proc Natal Acad Sci USA. 1984; 81: 24–94
   Google Scholar
• Lalor P A, Morahan G. The peritoneal Ly‐l (CD5) B cell repertoire is unique among murine B cell repertoires. Eur J Immunol. 1990; 20: 485–492
   Google Scholar
• Holmberg D. High connectivity, natural antibodies preferentially use 7183 and QUPC 52 VH families. Eur J Immunol. 1987; 17: 399–403
   Google Scholar
• Kaushik A, Lim A, Poncet P, Ge X ‐R, Dighiero G. Comparative analysis of natural antibody specificities among hybridomas originating from spleen and peritoneal cavity of adult NZB and BALB/c mice. Scand J Immunol. 1988; 27: 461–471
   PubMed Web of Science ®Google Scholar
• Haughton G, Arnold L W, Bishop G A, Mercolino T J. The CH series of murine B cell lymphomas: neoplastic analogues of Ly‐1+ normal B cells. Immunol Rev. 1986; 93: 35–51
   PubMedGoogle Scholar
• Schroeder H W, Jr, Hillson J L, Perlmutter R M. Structure and evolution of mammalian VH families. International Immunol. 1990; 2: 41–50
   PubMed Web of Science ®Google Scholar
• Briles D E, Forman C, Hudak S, Caflin J L. Anti‐phosphoryl‐choline antibodies of the T15 idiotype are optimally protective against. Streptococcus pneumoniae. J Exp Med. 1982; 156: 1177–1185
   PubMed Web of Science ®Google Scholar
• Scher I. The CBA/N mouse strain: an experimental model illustrating the influence of the X‐chromosome on immunity. Adv Immunol. 1982; 33: 2–71
   Google Scholar
• Weisman Duran L, Metcalf E S. Antibody‐defective, genetically susceptible CBA/N mice have an altered Salmonella typhimurium‐specific B cell repertoire. J Exp Med. 1987; 165: 29–46
   Google Scholar
• Hardy R R, Hayakawa K, Parks D R, Herzenberg L A. Demonstration of B cell maturation in X‐linked immunodeficient mice by simultaneous three‐colour immunofluorescence. Nature (London). 1983; 306: 270–272
   PubMed Web of Science ®Google Scholar
• Hayakawa K, Hardy R R, Herzenberg L A. Peritoneal Ly‐1 B cells: Genetic control, autoantibody production, increased lambda light chain expression. Eur J Immunol. 1986; 16: 450–456
   PubMed Web of Science ®Google Scholar
• Vaux D L, Lalor P A, Cory S, Johnson G R. In vivo expression of interleukin 5 induces an eosinophilia and expanded Ly‐l B lineage populations. International Immunol. 1990; 2: 965–971
   PubMed Web of Science ®Google Scholar
• Brdun J. Mechanisms of B Cell Neoplasia, F Melchers, M Potter. Roche, BasleSwitzerland 1987; 45–55
   Google Scholar
• Davidson W F, Pierce J H, Rudikoff S, Morse H C I I I. Relationship between B cell and myeloid differentiation. Studies with a B lymphocyte progenitor line, HAFTL‐I. J Exp Med. 1988; 168: 389–407
   PubMed Web of Science ®Google Scholar
• Weill J ‐C, Reynaud C ‐A. The chicken B cell compartment. Science 1987; 238: 1094–1098
   PubMed Web of Science ®Google Scholar
• Ratcliffe M J H, Ivanyi J. Allotype suppression in the chicken I. V. Deletion of B cells and lack of suppressor cells during chronic suppression. Eur J Immunol. 1981; 11: 306–310
   Google Scholar
• Pink J R, Ratcliffe M J H, Vainio O. Immunoglobulin‐bearing stem cells for clones of B (bursa‐derived) lymphocytes. Eur J Immunol. 1985; 15: 617–620
   Google Scholar
• Ratcliffe M J H, Lassila O, Pink J R L, Vainio O. Avian B cell precursors: surface immunoglobulin expression is an early, possibly bursa‐independent event. Eur J Immunol. 1986; 16: 129–133
   Google Scholar
• Spencer J, MacDonald T T, Finn T, Isaacson P G. The human gut contains a novel population of B lymphocytes which resemble marginal zone cells. Clin exp Immunol. 1985; 62: 607–612
   PubMed Web of Science ®Google Scholar
• Reynolds J D, Morris B. The evolution and involution of Peyer's patches in fetal and postnatal sheep. Eur J Immunol. 1983; 13: 627–635
   PubMedGoogle Scholar
• Reynolds J D, Morris B. Mitotic rate maturation in the Peyer's patches of fetal sheep and in the bursa of Fabricius of the chick embryo. Eur J Immunol. 1987; 17: 503–507
   Google Scholar
• Metcalf D. The Hemopoietic Colony Stimulating Factors. Elsevier Science Publishers B.V., AmsterdamThe Netherlands 1984
   Google Scholar
• Marcos M A R, Toribio M ‐L, de la Hera A, Marquez C, Gaspar M ‐L, Martinez A C. Mutual interactions and selection of immune repertoires. Immunol Today. 1988; 9: 204–207
   PubMedGoogle Scholar
• Ferrick D A, Ohashi P S, Wallace V, Schilham M, Mak T W. Thymic ontogeny and selection of αβ and Γδ cells. Immunol Today. 1989; 10: 403–407
   Google Scholar
• Raulet D H. The structure, function and molecular genetics of the Γ/δ cell receptor. Ann Rev Immunol. 1989; 7: 175–207
   PubMed Web of Science ®Google Scholar
• Linton P ‐J, Decker D J, Klinman N R. Primary antibody‐forming cells and secondary B cells are generated from separate precursor cell subpopulations. Cell. 1989; 59: 1049–1059
   PubMedGoogle Scholar