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Studies on in vitro IgE synthesis from lymph node cells of mice during infection with Nippostrongylus brasiliensis

Presence of inhibitory factor(s) in serum

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Abstract

The effect of serum factors on Ig synthesis (IgE, IgG) in vitro was analyzed. Spleen and mesenteric lymph node cells were obtained from Nippostrongylus brasiliensis-infected and non-infected mice. Sera and ammonium sulphate precipitated serum fractions from mice of different genetic origin (Balb/c - H-2d, A.CA - H-2f, B10.G - H-2q) suppressed in vitro IgE synthesis whereas a pronounced enhancement of IgG antibody synthesis was obtained in several experiments. Our results obtained with sera from both high and low IgE responder strains demonstrated that no strain specificity exists as to the inhibitory efficacy of mouse sera for total IgE synthesis in vitro. The suppressive activity of the mouse sera was concentrated in a fraction precipitated with 20%–50% saturated ammonium sulphate. Amicon XM50 ultrafiltration suggested that this fraction had an apparent molecular weight >50,000 daltons. Suppressive activity was removed by immunoadsorption of the 20–50% fraction with anti-IgE Sepharose. After exogenous addition of monoclonal IgE to an inactive fraction in vitro neither the fraction enriched in IgE nor monoclonal IgE alone were able to suppress IgE synthesis in the culture. Our results suggest that one or more serum factors in the presence of IgE are responsible for the suppression of total IgE synthesis in vitro.

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Abbreviations

BSA:

Bovine serum albumin

CFA:

Complete Freund's adjuvant

DNP:

Dinitrophenyl

EFA:

Enhancing factor of allergy

Fcɛ :

R Fcɛ-receptor for IgE

FCS:

Fetal calf serum

MLN:

Mesenteric lymph node

PBS:

Phosphate-buffered saline

PHA:

Phytohemagglutinin

PPD:

Purified protein derivative

SFA:

Suppressive factor of allergy

References

  • Bohn A, König W (1982a) Generation of monoclonal DNP-specific IgM and IgE murine antibodies, on the efficacy of hybridization. Mol Immunol 19:193–199

    Google Scholar 

  • Bohn A, König W (1982b) Generation of monoclonal murine anti-DNP-IgE, IgM and IgG1 antibodies: biochemical and biological characterization. Immunology 47:297–311

    Google Scholar 

  • Campbell DH, Garvey JS, Cremer NE, Sussdorf DH (1970) Methods in Immunology. 2nd Edit, WA Benjamin Inc, New York, pp 189–191

    Google Scholar 

  • Chiorazzi N, Fox DA, Katz DH (1976) Hapten-specific IgE antibody responses in mice. VI. Selective enhancement of IgE antibody production by low dose of X-irradiation and by cyclophosphamide. J Immunol 117:1629–1637

    Google Scholar 

  • Ishizaka K (1984) Regulation of IgE synthesis. Ann Rev Immunol 2:159–182

    Google Scholar 

  • Jardieu P, Uede T, Ishizaka K (1984) IgE-binding factors from mouse T lymphocytes. III. Role of antigen-specific suppressor T cells in the formation of IgE-suppressive factor. J Immunol 133:3266–3273

    Google Scholar 

  • Katz DH (1984) Regulaton of the IgE system: experimental and clinical aspects. Allergy 39:81–106

    Google Scholar 

  • Katz DH, Tung AS (1978) Regulation of IgE antibody production by serum molecules. II. Strain-specificity of the suppressive activity of serum from complete Freund's adjuvantimmune low responder mouse donors. J Immunol 120:2060–2067

    Google Scholar 

  • Katz DH, Bargatze RF, Bogowitz CA, Katz LR (1979) Regulation of IgE antibody production by serum molecules. IV. Complete Freund's adjuvant induces both enhancing and suppressive activities detectable in the serum of low and high responder mice. J Immunol 122:2184–2190

    Google Scholar 

  • Katz DH, Bargatze RF, Bogowitz CA, Katz LR (1980) Regulation of IgE antibody production by serum molecules. VII. The IgE-selective damping activity of suppressive factor of allergy (SFA) is exerted across both strain and species restriction barriers. J Immunol 124:819–824

    Google Scholar 

  • Katz DH, Chen S-S, Liu F-T, Bogowitz CA, Katz LR (1984) Biologically active molecules regulating the IgE antibody system: biochemical and biological comparisons of suppressive factor of allergy (SFA) and enhancing factor of allergy (EFA). J Mol Cell Immunol 1:157–166

    Google Scholar 

  • Kishimoto T (1982) IgE class-specific suppressor T cells and regulation of the IgE response. Prog Allergy 32:265–317

    Google Scholar 

  • Marcelletti JF, Katz DH (1984a) FcRɛ + lymphocytes and regulation of the IgE antibody system. I. A new class of molecules, termed IgE-induced regulants (EIR), which modulate FcRɛ expression by lymphocytes. J Immunol 133:2821–2828

    Google Scholar 

  • Marcelletti JF, Katz DH (1984b) FcRɛ + lymphocytes and regulation of the IgE antibody system. II. FcRɛ + B lymphocytes initiate a cascade of cellular and molecular interactions that control FcRɛ expression and IgE production. J Immunol 133:2829–2836

    Google Scholar 

  • Marcelletti JF, Katz DH (1984c) FcRɛ + lymphocytes and regulation of the IgE antibody system. III. Suppressive factor of allergy (SFA) is produced during the in vitro FcRɛ + expression cascade and displays corollary physiologic activity in vivo. J Immunol 133:2837–2844

    Google Scholar 

  • Marcelletti JF, Katz DH (1984d) FcRɛ + lymphocytes and regulation of the IgE antibody system. IV. Delineation of target cells and mechanisms of action of SFA and EFA in inhibitory in vitro induction of FcRɛ expression. J Immunol 133:2845–2851

    Google Scholar 

  • March SC, Parikh I, Cuatrecara P (1974) A simplified method for cyanogen bromide activation of agarose for affinity chromatography. Anal Biochem 60:149–152

    Google Scholar 

  • Nelson DS, Shneider CN (1974) Effect of normal mouse serum on mouse lymphocyte transformation in vitro. Eur J Immunol 4:79–86

    Google Scholar 

  • Ogilvie BM (1967) Reagin-like antibodies in rats infected with the nematode parasite Nippostrongylus brasiliensis. Immunology 12:113–131

    Google Scholar 

  • Ogilvie BM, Jones VE (1973) Immunity in the parasitic relationship between helminth and hosts. Prog Allergy 17:93–144

    Google Scholar 

  • Ovary Z (1982) IgE production and suppression in mice. Int Archs Allergy Appl Immun 66 (Suppl 1):8–18

    Google Scholar 

  • Pfeiffer P, König W, Bohn A (1983) Genetic dependence of IgE antibody production in mice infected with the nematode Nippostrongylus brasiliensis. I. Modulation of the IgE antibody response in vivo by serum factors. Int Archs Allergy Appl Immun 72:347–355

    Google Scholar 

  • Pfeiffer P, Rauschen I, Bohn A, König W (1985) IgE synthesis in vitro during infection of mice with the nematode Nippostrongylus brasiliensis: effects of mitogens and antigens. Z Parasitenkd 71:649–662

    Google Scholar 

  • Stockinger H, König W (1979) Inhibition of lymphocyte proliferation during parasitic infection with Nippostrongylus brasiliensis. In: Müller-Ruchholz W, Müller-Hermelink HK (eds), Function and structure of the immune system, Plenum Publ Corp, New York, p 693

    Google Scholar 

  • Tung AS, Chiorazzi N, Katz DH (1978) Regulation of IgE antibody production by serum molecules. I. Serum from complete Freund's adjuvant-immune donors suppresses irradiation-enhanced IgE production in low responder mouse strains. J Immunol 120:2050–2059

    Google Scholar 

  • Uede T, Ishizaka K (1984) IgE-binding factors from mouse T lymphocytes. II. Strain differences in the nature of IgE-binding factor. J Immunol 133:359–367

    Google Scholar 

  • Uede T, Sandberg K, Bloom BR, Ishizaka K (1983) IgE-binding factors from mouse T lymphocytes. I. Formation of IgE-binding factors by stimulation with homologous IgE and interferon. J Immunol 130:649–654

    Google Scholar 

  • Vander-Mallie R, Ishizaka T, Ishizaka K (1982) Lymphocytes bearing Fc receptors for IgE. VIII. Affinity of mouse IgE for FcɛR on mouse B lymphocytes. J Immunol 128:2306–2312

    Google Scholar 

  • Veit BC, Michael JG (1972) Immune response suppression by an inhibitor in normal and immune mouse serum. Nature 235:238–240

    Google Scholar 

  • Veit BC, Michael JG (1973) Characterization of an immunosuppressive factor in present in mouse serum. J Immunol 111:341–351

    Google Scholar 

  • Walker SM, Sturtevant JE, Weigle WO (1981) Serum-mediated suppression of non-specific B cell activation. I. Description of an inhibitory capacity in normal mouse serum and characterization of the inhibitory component. J Immunol 126:1852–1856

    Google Scholar 

  • Watanabe N, Ovary Z (1977) Suppression of IgE antibody production in SJL mice. III: Characterization of a suppressor substance extracted from normal SJL spleen cells. J Exp Med 145:1501–1510

    Google Scholar 

  • Watanabe N, Kojima S, Ovary Z (1976) Suppression of IgE antibody production in SJL mice. I. Nonspecific suppressor T cells. J Exp Med 143:833–845

    Google Scholar 

  • Watanabe N, Kojima S, Shen F-W, Ovary Z (1977) Suppression of IgE antibody production in SJL mice. II. Expression of Ly-1 antigen on helper and nonspecific suppressor T cells. J Immunol 118:485–488

    Google Scholar 

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Pfeiffer, P., Rauschen, I. & König, W. Studies on in vitro IgE synthesis from lymph node cells of mice during infection with Nippostrongylus brasiliensis . Parasitol Res 73, 87–94 (1987). https://doi.org/10.1007/BF00536341

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