Abstract
The process by which secondary B cells are generated has intrigued immunologists for several decades. This is particularly true since appropriate antigenic stimulation leads both to a selective increase in the frequency of B cells responsive to the immunizing antigen and to the generation of a population of cells (secondary B cells) that are phenotypically and functionally distinct from primary B cells specific for the same antigen.
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References
Berek C, Griffiths GM, Milstein C (1985) Molecular events during maturation of the immune response to oxazolone. Nature 316: 412–418
Black SJ, Van der Loo W, Loken MR, Herzenberg LA (1977) Expression of IgD indicates maturation of memory B cells. J Exp Med 147: 984–996
Bruce J, Symington FW, McKearn TJ, Sprent J (1981) A monoclonal antibody discriminating between subsets of T and B cells. J Immunol 127: 2496–2501
Cambier JC, Kettman JR, Vitetta ES, Uhr JW (1976) Differential suspectibility of neonatal and adult murine spleen cells to in vitro induction of B cell tolerance. J Exp Med 144: 293–297
Cancro MP, Gerhard W, Klinman NR (1978) Diversity of the primary influenza specific B cell repertoire in BALB/c mice. J Exp Med 147: 776–778
Clarke SH, Huppi K, Ruezinsky D, Staudt L, Gerhard W, Weigert M (1985) Inter- and intraclonal diversity in the antibody response to influenza hemagglutinin. J Exp Med 161: 687–704
Coffman RL and Carty J (1986) A T cell activity that enhances polyclonal IgE production and its inhibition by interferon-gamma. J Immunol 136: 949–954
Coffman RL, Ohara J, Bond MW, Carty J, Zlotnick E, Paul WE (1986) B cell stimulatory factor 1 enhances the IgE response of lipopolysaccharide preactivated B cells. J Immunol 136: 4538–4541
Duran LW, Metcalf ES (1987) Clonal analysis of primary B cells responsive to the pathogenic bacterium Salmonella typhimurium. J Exp Med 165: 340–358
Eisen HN, Siskind GW (1964) Variation in affinities of antibodies during the immune response. Biochemistry 3: 996–1008
Eisen HN, Little RJ, Steiner LA, Simms ES, Gray WG (1969) Degeneracy in the secondary immune response: stimulation of antibody formation by cross-reacting antigens. Isr J Med Sci 5: 338–351
Elson CJ, Jablonska KF, Taylor RB (1976) Functional half-life of virgin and primed B lymphocytes. Eur J Immunol 6: 634–638
Fazekas de St. Groth S, Webster RG (1966) Disquisitions on original antigenic sin I. Evidence in man. J Exp Med 124: 331–345
Finkelman FD, Katona IM, Mosmann TR, Coffman RL (1988) Interferon γ regulates the isotypes of immunoglobulin secreted during in vivo humoral responses. J Immunol 140: 1022–1027
Froscher BG, Klinman NR (1985) Strain specific silencing of a predominant anti-dextran clonotype family. J Exp Med 162: 1620–1633
Gearhart PJ, Sigal NH, Klinman NR (1975) Production of antibodies of identical idiotype but diverse immunoglobulin classes by cells derived from a single stimulated B cell. Proc Natl Acad Sci USA 72:1707–1711
Jemmerson RW (1987) Multiple overlapping epitopes in the three antigenic regions of horse cytochrome c. J Immunol 138: 213–219
Kaplan MA, Ching LK, Berte C, Sercarz EE (1985) Predominant idiotypy and specificity shift during the antibody response to lysozyme (abstract). Fed Proc 44: 1692
Karjalainen K, Bang B, Makela O (1980) Fine specificity and idiotypes of early antibodies against (4- hydroxy-3-nitrophenyl)acetyl (NP). J Immunol 125: 313–317
Kim S, Davis M, Sinn E, Patten P, Hood L (1981) Antibody diversity: somatic hypermutation of rearranged Vh genes. Cell 27: 573–581
Klinman NR (1972) The mechanism of antigen stimulation of primary and secondary clonal precursor cells. J Exp Med 136: 241–260
Klinman NR (1976) The acquisition of B cell competence and diversity. Am J Pathol 85: 694–703
Klinman NR, Linton P-J (1988) The clonotype repertoire of B cell subpopulations. Adv Immunol 42:1–93
Klinman NR, Press JL (1975) The B cell specificity repertoire: its relationship to definable subpopulations. Transplant Rev 24: 41–83
Klinman NR, Stone MR (1983) The role of variable region gene expression and environmental selection in determining the anti-phosphorylcholine B cell repertoire. J Exp Med 158: 1948–1961
Klinman NR, Rockey JH, Frauenberger G, Karush F (1966) Equine antihapten antibody. III. The comparative properties of the γG- and γA antibodies
Klinman NR, Press JL, Segal GP (1973) Overlap stimulation of primary and secondary B cells by cross-reacting determinants. J Exp Med 138: 1276–1281
Klinman NR, Press JL, Pickard AR, Woodland RT, Dewey AF (1974) Biography of the B cell. In: Sercarz E, Williamson A, Fox CF (eds) The immune system. Academic, New York, pp 357–365
Klinman NR, Pickard AR, Sigal NK, Gearhart PJ, Metcalf ES, Pierce SK (1976) Assessing B cell diversification by antigen receptor and precursor cell analysis. Ann Immunol 127: 489–502
Krawinkel U, Zoebelein G, Burggemann M, Radbruch M, Rajewsky K (1983) Recombination between antibody heavy chain variable-region genes: evidence for gene conversion. Proc Natl Acad Sci USA 80: 4997–5001
Linton P-J, Klinman, NR (1986) The generation of secondary B cells in vitro (abstract). Fed Proc 45:378
Linton P-J, Gilmore GL, Klinman NR (1988) The secondary B cell lineage. In: Witte O, Howard M, Klinman NR (eds) B cell development. UCLA Symposia on Molecular and Cellular Biology, New Series, vol 85. Liss, New York
Linton PJ, Decker DJ, Klinman NR (1989) Primary antibody-forming cells and secondary B cells are generated from separate precursor cell subpopulations. Cell 59: 1049–1059
MacLennan ICM, Gray D (1986) Antigen-driven selection of virgin and memory B cells. Immunol Rev 91: 61–85
Makela O, Karjalainen K (1977) Inherited immunoglobulin idiotypes of the mouse. Immunol Rev 34:119–138
Manser T (1987) Mitogen-driven B cell proliferation and differentiation are not accompanied by hypermutation of immunoglobulin variable region genes. J Immunol 139: 234–238
Manser T, Wysocki LJ, Margolies MN, Gefter ML (1987) Evolution of antibody variable region structure during the immune response. Immunol Rev 96: 141–162
McKean D, Huppi K, Bell M, Staudt L, Gerhard W, Weigert M (1984) Generation of antibody diversity in the immune response of BALB/c mice to influenza virus hemagglutinin. Proc Natl Acad Sci USA 81:3180–3184
Metcalf ES, Klinman NR (1976) In vitro tolerance induction of neonatal murine B Cells. J Exp Med 143:1327–1340
Metcalf ES, Klinman NR (1977) In vitro tolerance of bone marrow cells: a marker for B cell maturation. J Immunol 118: 2111–2116
Morrow PR, Jemmerson RRW, Klinman NR (1987) Disparities in the repertoire of B cells responsive to a native protein and those responsive to a synthetic peptide. In: Sercarz EE, Berzofsky J (eds) Immunogenicity of protein antigens: repertoire and regulation, vol II. Academic, Orlando, pp 43–49
Mosmann TR, Cherwinski H, Bond MW, Giedlin MA, Coffman RL (1986) Two types of murine helper T cell clones. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol 136: 2348–2357
Nossal G, Warner N, Lewis H (1971) Incidence of cells simultaneously secreting IgM and IgG antibody to sheep erythrocytes. Cell Immunol 2: 41–53.
Nossal GJV, Pike BL (1975) Evidence for the clonal abortion theory of B lymphocyte tolerance. J Exp Med 141:904–917
Owen FL, Nisonoff A (1978) Effect of idiotype-specific suppressor T cells on primary and secondary responses. J Exp Med 148: 182–194
Perlmutter RM, Crews ST, Douglas R, Sorensen G, Johnson N, Nivera N, Gearhart PJ, Hood L (1984) The generation of diversity in phosphorylcholine binding antibodies. Adv Immunol 35: 1–37
Pierce SK, Klinman NR (1977) Antibody-specific immunoregulation. J Exp Med 146: 509–519
Press JL, Klinman NR (1973) Monoclonal production of both IgM and IgG1 anti-hapten antibody. J Exp Med 135: 300–305
Raychaudhuri S, Cancro MP (1985) Cellular basis for neonatally induced T-suppressor activity. J Exp Med 161:816–831
Riley RL, Klinman NR (1985) Differences in antibody repertoires for (4-hydroxy-3-nitrophenyl)acetyl (NP) in splenic vs immature bone marrow precursor cells. J Immunol 135: 3050–3055
Riley RL, Klinman NR (1986) The affinity threshold for antigenic triggering differs for tolerance susceptible immature precursors vs mature primary B cells. J Immunol 136: 3147–3154
Riley RL, Wylie DE, Klinman NR (1983) B cell repertoire diversification precedes immunoglobulin receptor expression. J Exp Med 158: 1733–1738
Seising E, Storb U (1981) Somatic mutation of immunoglobulin light chain variable region genes. Cell 25:47–58
Siekevitz M, Kocks C, Rajewsky K, Dildrop R (1987) Analysis of somatic mutation and class switching in naive and memory B cells generating adoptive primary and secondary responses. Cell 48; 757–770
Sigal NH, Klinman NR (1978) The B cell clonotype repertoire. Adv Immunol 26: 255–337
Stashenko P, Klinman NR (1980) Analysis of the primary anti-(4-hydroxy-3-nitrophenyl)acetyl (NP) responsive B cells in BALB/c and B10.D2 mice. J Immunol 125: 531–537
Stocker JW (1977) Tolerance induction in maturing B cells. Immunology 32: 282–290
Strober S (1972) Initiation of antibody responses by different classes of lymphocytes. V. Fundamental changes in the physiological characteristics of virgin thymus-independent (“B”) lymphocytes and “B” memory cells. J Exp Med 136: 851–871
Symington FW, Hakemori S-I (1984) Hematopoietic subpopulations express cross-reactive, lineage- specific molecules detected by monoclonal antibody. Mol Immunol 21: 507–514
Teale JM, Klinman NR (1980) Tolerance as an active process. Nature 288: 385–386
Teale JM, Klinman NR (1984) Membrane and metabolic requirements for tolerance induction of neonatal B cells. J Immunol 133: 1811–1817
Teale JM, Lafrenz D, Klinman NR, Strober S (1981) Immunoglobulin class commitment exhibited by B lymphocytes separated according to surface isotype. J Immunol 126: 1952–1957
Wang A, Wilson A, Hopper J, Fudenberg H, Nisonoff A (1970) Evidence for control of synthesis of the variable regions of the heavy chains of immunoglobulins G and M by the same gene. Proc Natl Acad Sci USA 66: 337–343
Williamson AR, Zitron IM, McMichael AJ (1976) Clones of B lymphocytes: their natural selection and expansion. Fed Proc 35: 2195–2201
Yokota T, Arai N, de Vries JE, Spits H, Banchereau J, Zlotnick A, Rennick D, Howard M, Takebe Y, Miyatake S, Lee F, Arai K (1988) Molecular biology of interleukin 4 and interleukin 5 genes and biology of their products that stimulate B cells, T cells and hemopoietic cells. Immunol Rev 102: 137–187
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Klinman, N.R., Linton, PJ. (1990). The Generation of B-Cell Memory: A Working Hypothesis. In: Gray, D., Sprent, J. (eds) Immunological Memory. Current Topics in Microbiology and Immunology, vol 159. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75244-5_2
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DOI: https://doi.org/10.1007/978-3-642-75244-5_2
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