It will be attempted to produce monoclonal antibodies against allotype 7a and 7b, the two most important allotypes of murine IgE, the antibody responsible for anaphylactic reactions. Allotype 7b does not crossreact with any other allotype T antibodies and allotype 7a crossreacts with all the other allotype 7 antibodies except with allotype 7b. These two monoclonal antibodies (anti-7a and anti-7b) would be of great importance for research in experimental allergic reactions. For the production of these monoclonal antibodies the hybridoma technique will be used. Spleen cells from inbred mice immunized against allotype 7a or 7b and producing anti-7a or anti-7b antibodies will be fused with a nonproducing myeloma cell and the hybridoma cells obtained will be checked for the production of anti-7a or anti-7b monoclonal antibodies, using as test passive hemagglutination of sheep red blood cells coated with 7a or 7b IgE antibodies. T cells from inbred mice primed with well defined immunogenic antigens, will be cloned, using a standard method of T cell cloning. Long term cultures will be established from those cell lines which have specificity for the antigen demonstrated by radiolabeled thymidine incorporation. These T cell lines will be then tested in vitro for antigen specific help using primed B cells from inbred mice syngeneic to the mice from which the T cells were cloned. The B cells will be from mice primed with hapten-carrier protein complex, but the carrier protein will be different from that used to prime the T cells. In the in vitro tests the same hapten that was used for priming the B cells will be coupled to the antigen used for the T cells. In this way it will be possible to ascertain antigen specific help by the T cells and the role of these T cells in production of different murine isotypes, especially IgE antibody. T cells from SJA9 mice taken from mice infected with Nippostrongylus brasiliensis will be cloned on feeder cells from Nippostrongylus infected mice. It will be attempted to clone by this procedure the T cell which brings about the switch for IgE production in this strain. The cloned T cells will be tested in SJA9 mice in vivo and also with SJA9 spleen cells from primed mice in vitro.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI003075-29
Application #
3124121
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1974-12-01
Project End
1990-03-31
Budget Start
1988-09-01
Budget End
1990-03-31
Support Year
29
Fiscal Year
1988
Total Cost
Indirect Cost
Name
New York University
Department
Type
Schools of Medicine
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
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Ueda, A; Chandswang, N; Ovary, Z (1990) The action of interleukin-4 on antigen-specific IgG1 and IgE production by interaction of in vivo primed B cells and carrier-specific cloned Th2 cells. Cell Immunol 128:31-40
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Watanabe, N; Katakura, K; Kobayashi, A et al. (1988) Protective immunity and eosinophilia in IgE-deficient SJA/9 mice infected with Nippostrongylus brasiliensis and Trichinella spiralis. Proc Natl Acad Sci U S A 85:4460-2
Furusawa, S; Ovary, Z (1988) Heteroclitic antibodies: differences in fine specificities between monoclonal antibodies directed against dinitrophenyl and trinitrophenyl haptens. Int Arch Allergy Appl Immunol 85:238-43
Hirano, T; Miyajima, H; Kitagawa, H et al. (1988) Studies on murine IgE with monoclonal antibodies. I. Characterization of rat monoclonal anti-IgE antibodies and the use of these antibodies for determinations of serum IgE levels and for anaphylactic reactions. Int Arch Allergy Appl Immunol 85:47-54
Azuma, M; Hirano, T; Miyajima, H et al. (1987) Regulation of murine IgE production in SJA/9 and nude mice. Potentiation of IgE production by recombinant interleukin 4. J Immunol 139:2538-44
Emancipator, S N; Ovary, Z; Lamm, M E (1987) Immunological injury in IgA nephropathy. Adv Exp Med Biol 216B:1477-87

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