The donor cell type controls anti-hapten (fluorescein isothiocyanate) primary antibody response to hapten-modified syngeneic cells. 1982

K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito

Hapten (fluorescein isothiocyanate, FITC)-sensitized syngeneic red blood cells (FITC-RBC) are exceptionally active for induction of anti-hapten primary antibody response, and FITC-modified syngeneic spleen cells depleted of RBC (FITC-SSC) are not immunogenic [4]. The present study has demonstrated that FITC-SSC injected simultaneously with FITC-RBC inhibit partially the anti-FITC response to the latter. Either the immunogenicity of FITC-RBC or the response-inhibiting activity of FITC-SSC was increased as the concentration of hapten-sensitizing cells was raised from 0.005 mg/ml to 2 mg/ml. The inhibition of anti-FITC response by FITC-SSC strictly required live donor cells, but was not dependent on T-cell activity of either the donor or recipient. Neither FITC-thymocytes nor the FITC-T-cell-rich fraction of SSC showed a definite activity for inhibition, whereas the FITC-B-cell-rich fraction of SSC acted very effectively. These results suggest that the primary anti-hapten antibody response to hapten-modified syngeneic cells is primarily controlled by antigen-bearing live donor cells of different cell types.

UI MeSH Term Description Entries
D008297 Male Males
D008815 Mice, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations, or by parent x offspring matings carried out with certain restrictions. All animals within an inbred strain trace back to a common ancestor in the twentieth generation. Inbred Mouse Strains,Inbred Strain of Mice,Inbred Strain of Mouse,Inbred Strains of Mice,Mouse, Inbred Strain,Inbred Mouse Strain,Mouse Inbred Strain,Mouse Inbred Strains,Mouse Strain, Inbred,Mouse Strains, Inbred,Strain, Inbred Mouse,Strains, Inbred Mouse
D008819 Mice, Nude Mutant mice homozygous for the recessive gene "nude" which fail to develop a thymus. They are useful in tumor studies and studies on immune responses. Athymic Mice,Mice, Athymic,Nude Mice,Mouse, Athymic,Mouse, Nude,Athymic Mouse,Nude Mouse
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D005260 Female Females
D005452 Fluoresceins A family of spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one derivatives. These are used as dyes, as indicators for various metals, and as fluorescent labels in immunoassays. Tetraiodofluorescein
D005456 Fluorescent Dyes Chemicals that emit light after excitation by light. The wave length of the emitted light is usually longer than that of the incident light. Fluorochromes are substances that cause fluorescence in other substances, i.e., dyes used to mark or label other compounds with fluorescent tags. Flourescent Agent,Fluorescent Dye,Fluorescent Probe,Fluorescent Probes,Fluorochrome,Fluorochromes,Fluorogenic Substrates,Fluorescence Agents,Fluorescent Agents,Fluorogenic Substrate,Agents, Fluorescence,Agents, Fluorescent,Dyes, Fluorescent,Probes, Fluorescent,Substrates, Fluorogenic
D006241 Haptens Small antigenic determinants capable of eliciting an immune response only when coupled to a carrier. Haptens bind to antibodies but by themselves cannot elicit an antibody response. Hapten,Contact-Sensitizing Agents,Agents, Contact-Sensitizing,Contact Sensitizing Agents
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000917 Antibody Formation The production of ANTIBODIES by proliferating and differentiated B-LYMPHOCYTES under stimulation by ANTIGENS. Antibody Production,Antibody Response,Antibody Responses,Formation, Antibody,Production, Antibody,Response, Antibody,Responses, Antibody

Related Publications

K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
November 1981, European journal of immunology,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
December 1986, European journal of immunology,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
October 1987, Cellular immunology,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
July 2004, Analytical biochemistry,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
December 2000, Analytical biochemistry,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
November 1971, European journal of immunology,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
January 1981, Scandinavian journal of immunology,
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
September 1982, Journal of immunology (Baltimore, Md. : 1950),
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
February 1976, Journal of immunology (Baltimore, Md. : 1950),
K Suzuki, and I Nakashima, and M Takashi, and F Nagase, and N Kato, and K Isobe, and K Mizoguchi, and M Saito
January 1975, Transplantation reviews,
Copied contents to your clipboard!