The central focus of the proposed research is to determine the genetic and regulatory influences determining the quantity and quality of antibody produced in an immune response. In particular, we are examining the response to a defined hapten by inbred mice. We have characterized the genes controlling expression of antibody bearing a particular idiotype, an antigenic determinant borne by anti-2,4-dinitrophenyl (DNP) antibody in certain strains of inbred mice. Genes encoding the variable regions of both light and heavy immunoglobulin polypeptide chains are involved in the expression of this idiotype. Secondly, we have determined the kinetics of idiotype of expression. The idiotype is transiently dominant during secondary antibody responses. Third, we have examined the question of whether this regulation of idiotype can also account for the regulation of the expression of different constant region of immunoglobulin gene products. Our results suggest that the regulation of constant region gene expression is an independent process from the regulation of variable region gene products. Finally, we have sought an explanation of the reason for preferential expression of this particular idiotype. We have found that the idiotype is found in significant amounts in normal serum, but in that form does not bind the antigen DNP. We have prepared such idiotype positive, non-DNP binding material as a monoclonal antibody in order to determine the antigens which induce its expression. It is our hypothesis that this idiotypic material activates a set of idiotype-specific helper T cells, which in turn activate DNP-specific, idiotypic B cells also activated by conventional helper T cells. We are currently testing this hypothesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI013766-09
Application #
3125553
Study Section
(SSS)
Project Start
1977-04-01
Project End
1988-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
9
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
Portoles, P; Rojo, J M; Janeway Jr, C A (1990) A simple method for the radioactive iodination of CD4 molecules. J Immunol Methods 129:105-9
Portoles, P; Janeway Jr, C A (1989) Inhibition of the responses of a cloned CD4+ T cell line to different class II major histocompatibility complex ligands by anti-CD4 and by anti-receptor Fab fragments are directly related. Eur J Immunol 19:83-7
Portoles, P; Rojo, J M; Janeway Jr, C A (1989) Asymmetry in the recognition of antigen: self class II MHC and non-self class II MHC molecules by the same T-cell receptor. J Mol Cell Immunol 4:129-37
Marion, T N; Bothwell, A L; Briles, D E et al. (1989) IgG anti-DNA autoantibodies within an individual autoimmune mouse are the products of clonal selection. J Immunol 142:4269-74
Janeway Jr, C A; Yagi, J; Rojo, J et al. (1988) Immune recognition and effector function in subsets of CD4 T cells. Princess Takamatsu Symp 19:193-208
Janeway Jr, C A; Carding, S; Jones, B et al. (1988) CD4+ T cells: specificity and function. Immunol Rev 101:39-80
Janeway Jr, C A; Broughton, B; Smith, L A et al. (1987) Direct receptor:receptor interactions between T and B lymphocytes: idiotypic restriction in the antibody response to a cloned helper T cell receptor. J Mol Cell Immunol 3:83-94
Blier, P R; Bothwell, A (1987) A limited number of B cell lineages generates the heterogeneity of a secondary immune response. J Immunol 139:3996-4006
Dzierzak, E A; Janeway Jr, C A; Richard, N et al. (1986) Molecular characterization of antibodies bearing Id-460. I. The structure of two highly homologous VH genes used to produce idiotype positive immunoglobulins. J Immunol 136:1864-70
Tite, J P; Kaye, J; Saizawa, K M et al. (1986) Direct interactions between B and T lymphocytes bearing complementary receptors. J Exp Med 163:189-202

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