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. 1997 Aug;65(8):3203–3208. doi: 10.1128/iai.65.8.3203-3208.1997

Neisserial porins may provide critical second signals to polysaccharide-activated murine B cells for induction of immunoglobulin secretion.

C M Snapper 1, F R Rosas 1, M R Kehry 1, J J Mond 1, L M Wetzler 1
PMCID: PMC175453  PMID: 9234776

Abstract

Resting B cells stimulated with dextran-conjugated anti-immunoglobulin D (anti-IgD) antibodies (anti-Ig-dex), a model for B-cell activation in response to polysaccharide antigens, proliferate but secrete little if any Ig, unless additional stimuli are present. In order to elucidate the parameters which costimulate T-cell-independent antipolysaccharide antibody responses during bacterial infections, we tested the capacities of highly purified porin proteins from Neisseria meningitidis and Neisseria gonorrhoeae to augment in vitro proliferation and induce Ig secretion by anti-Ig-dex-activated B cells. Resting B cells, from lipopolysaccharide (LPS)-nonresponsive C3H/HeJ mice, proliferated and secreted IgM in response to each of three distinct porins acting alone. Further, porins, even at concentrations that were minimally inductive when acting alone, were strongly synergistic with anti-Ig-dex for proliferation and Ig secretion. Similar synergistic effects of porins with CD40-ligand were also observed. These effects of porins were shown to occur directly at the level of the B cell. The predominant Ig isotype elicited in response to porins plus anti-Ig-dex or CD40-ligand was IgM (>97%), with the remainder comprising IgG. Surprisingly, picogram-per-milliliter amounts of neisserial LPS were also found to be highly synergistic with anti-Ig-dex for induction of IgM secretion by LPS-responsive C3H/HeN, but not C3H/HeJ, B cells. Thus, these data suggest that porins, as well as LPS, may provide critical second signals for T-cell-independent induction of polysaccharide-specific Ig in response to neisserial and other gram-negative porin-expressing bacterial pathogens, without a requirement for the participation of non-B cell types. These data may also help to explain the potent immunopotentiating effects of porins for polysaccharide-specific, as well as protein-specific, humoral responses in vivo.

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Selected References

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  1. Brunswick M., Finkelman F. D., Highet P. F., Inman J. K., Dintzis H. M., Mond J. J. Picogram quantities of anti-Ig antibodies coupled to dextran induce B cell proliferation. J Immunol. 1988 May 15;140(10):3364–3372. [PubMed] [Google Scholar]
  2. Coutinho A., Möller G. Thymus-independent B-cell induction and paralysis. Adv Immunol. 1975;21:113–236. doi: 10.1016/s0065-2776(08)60220-5. [DOI] [PubMed] [Google Scholar]
  3. Donnelly J. J., Deck R. R., Liu M. A. Immunogenicity of a Haemophilus influenzae polysaccharide-Neisseria meningitidis outer membrane protein complex conjugate vaccine. J Immunol. 1990 Nov 1;145(9):3071–3079. [PubMed] [Google Scholar]
  4. Guttormsen H. K., Wetzler L. M., Naess A. Humoral immune response to the class 3 outer membrane protein during the course of meningococcal disease. Infect Immun. 1993 Nov;61(11):4734–4742. doi: 10.1128/iai.61.11.4734-4742.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kearney J. F., Cooper M. D., Lawton A. R. B lymphocyte differentiation induced by lipopolysaccharide. III. Suppression of B cell maturation by anti-mouse immunoglobulin antibodies. J Immunol. 1976 Jun;116(6):1664–1668. [PubMed] [Google Scholar]
  6. Kearney J. F., Klein J., Bockman D. E., Cooper M. D., Lawton A. R. B cell differentiation induced by lipopolysaccharide. V. Suppression of plasma cell maturation by anti-mu: mode of action and characteristics of suppressed cells. J Immunol. 1978 Jan;120(1):158–166. [PubMed] [Google Scholar]
  7. Kearney J. F., Lawton A. R. B lymphocyte differentiation induced by lipopolysaccharide. I. Generation of cells synthesizing four major immunoglobulin classes. J Immunol. 1975 Sep;115(3):671–676. [PubMed] [Google Scholar]
  8. Kehry M. R., Castle B. E. Regulation of CD40 ligand expression and use of recombinant CD40 ligand for studying B cell growth and differentiation. Semin Immunol. 1994 Oct;6(5):287–294. doi: 10.1006/smim.1994.1037. [DOI] [PubMed] [Google Scholar]
  9. Livingston P. O., Calves M. J., Helling F., Zollinger W. D., Blake M. S., Lowell G. H. GD3/proteosome vaccines induce consistent IgM antibodies against the ganglioside GD3. Vaccine. 1993 Sep;11(12):1199–1204. doi: 10.1016/0264-410x(93)90043-w. [DOI] [PubMed] [Google Scholar]
  10. Lowell G. H., Ballou W. R., Smith L. F., Wirtz R. A., Zollinger W. D., Hockmeyer W. T. Proteosome-lipopeptide vaccines: enhancement of immunogenicity for malaria CS peptides. Science. 1988 May 6;240(4853):800–802. doi: 10.1126/science.2452484. [DOI] [PubMed] [Google Scholar]
  11. Mond J. J., Lees A., Snapper C. M. T cell-independent antigens type 2. Annu Rev Immunol. 1995;13:655–692. doi: 10.1146/annurev.iy.13.040195.003255. [DOI] [PubMed] [Google Scholar]
  12. Mond J. J. Use of the T lymphocyte regulated type 2 antigens for the analysis of responsiveness of Lyb5+ and Lyb5- B lymphocytes to T lymphocyte derived factors. Immunol Rev. 1982;64:99–115. doi: 10.1111/j.1600-065x.1982.tb00420.x. [DOI] [PubMed] [Google Scholar]
  13. Parker D. C. T cell-dependent B cell activation. Annu Rev Immunol. 1993;11:331–360. doi: 10.1146/annurev.iy.11.040193.001555. [DOI] [PubMed] [Google Scholar]
  14. Peçanha L. M., Snapper C. M., Finkelman F. D., Mond J. J. Dextran-conjugated anti-Ig antibodies as a model for T cell-independent type 2 antigen-mediated stimulation of Ig secretion in vitro. I. Lymphokine dependence. J Immunol. 1991 Feb 1;146(3):833–839. [PubMed] [Google Scholar]
  15. Peçanha L. M., Yamaguchi H., Lees A., Noelle R. J., Mond J. J., Snapper C. M. Dextran-conjugated anti-IgD antibodies inhibit T cell-mediated IgE production but augment the synthesis of IgM and IgG. J Immunol. 1993 Mar 15;150(6):2160–2168. [PubMed] [Google Scholar]
  16. Snapper C. M., Mond J. J. A model for induction of T cell-independent humoral immunity in response to polysaccharide antigens. J Immunol. 1996 Sep 15;157(6):2229–2233. [PubMed] [Google Scholar]
  17. Snapper C. M., Mond J. J. Towards a comprehensive view of immunoglobulin class switching. Immunol Today. 1993 Jan;14(1):15–17. doi: 10.1016/0167-5699(93)90318-F. [DOI] [PubMed] [Google Scholar]
  18. Snapper C. M., Rosas F. R., Jin L., Wortham C., Kehry M. R., Mond J. J. Bacterial lipoproteins may substitute for cytokines in the humoral immune response to T cell-independent type II antigens. J Immunol. 1995 Dec 15;155(12):5582–5589. [PubMed] [Google Scholar]
  19. Sultzer B. M., Castagna R., Bandekar J., Wong P. Lipopolysaccharide nonresponder cells: the C3H/HeJ defect. Immunobiology. 1993 Apr;187(3-5):257–271. doi: 10.1016/S0171-2985(11)80343-8. [DOI] [PubMed] [Google Scholar]
  20. Vetvicka V., Lee G., Kincade P. W. Intrinsic B lymphocyte and macrophage defects in C3H/HeJ mice. J Immunol. 1986 Apr 1;136(7):2370–2374. [PubMed] [Google Scholar]
  21. Vordermeier H. M., Bessler W. G. Polyclonal activation of murine B lymphocytes in vitro by Salmonella typhimurium porins. Immunobiology. 1987 Sep;175(3):245–251. doi: 10.1016/S0171-2985(87)80033-5. [DOI] [PubMed] [Google Scholar]
  22. Vordermeier H. M., Drexler H., Bessler W. G. Polyclonal activation of human peripheral blood lymphocytes by bacterial porins and defined porin fragments. Immunol Lett. 1987 Jun;15(2):121–126. doi: 10.1016/0165-2478(87)90042-3. [DOI] [PubMed] [Google Scholar]
  23. Wetzler L. M., Blake M. S., Barry K., Gotschlich E. C. Gonococcal porin vaccine evaluation: comparison of Por proteosomes, liposomes, and blebs isolated from rmp deletion mutants. J Infect Dis. 1992 Sep;166(3):551–555. doi: 10.1093/infdis/166.3.551. [DOI] [PubMed] [Google Scholar]
  24. Wetzler L. M., Blake M. S., Gotschlich E. C. Characterization and specificity of antibodies to protein I of Neisseria gonorrhoeae produced by injection with various protein I-adjuvant preparations. J Exp Med. 1988 Nov 1;168(5):1883–1897. doi: 10.1084/jem.168.5.1883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Wetzler L. M., Gotschlich E. C., Blake M. S., Koomey J. M. The construction and characterization of Neisseria gonorrhoeae lacking protein III in its outer membrane. J Exp Med. 1989 Jun 1;169(6):2199–2209. doi: 10.1084/jem.169.6.2199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Wetzler L. M., Ho Y., Reiser H., Wetzler L. W. Neisserial porins induce B lymphocytes to express costimulatory B7-2 molecules and to proliferate. J Exp Med. 1996 Mar 1;183(3):1151–1159. doi: 10.1084/jem.183.3.1151. [DOI] [PMC free article] [PubMed] [Google Scholar]

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