Abstract
Anti-p-azobenzenearsonate (ABA) antibodies, coupled covalently to normal syngeneic spleen cells and then given intravenously to normal animals, were found to be potent tolerogens for delayed-type hypersensitivity (DTH) to ABA. The ability of the antibody-coupled cells to induce tolerance was determined to be a result of the cross-reactive idiotype (CRI+) fraction of the antibodies, because anti-ABA antibodies lacking the CRI+ components when coupled to spleen cells were unable to cause any significant inhibition. Furthermore, genetic analysis revealed that the ability of CRI-coupled cells to inhibit ABA-specific DTH is linked to Igh-1 heavy chain allotype, in as much animals which possess heavy chain allotypes similar to that of A/J were sensitive to this inhibition. Adoptive transfer experiments provided evidence that CRI-coupled cells induce suppressor cells, and spleen cells or thymocytes from animals received CRI-coupled cells were able to transfer suppression to naive recipients. In addition, treatment with anti-Thy1.2 serum plus complement completely abrogated their ability to transfer suppression. Thus, this active suppression is a T-cell-dependent phenomenon. In investigating the specificity of these suppressor T cells, it was found that they functioned in an antigen-specific manner and were unable to suppress the development of DTH to an unrelated hapten 2,4-dinitro-1-fluorobenzene.
MeSH Terms
Animals
Cross Reactions
Epitopes
Female
Hypersensitivity, Delayed
Immunosuppression Therapy
Isoantibodies/immunology
Mice
Mice, Inbred A/immunology
Mice, Inbred BALB C/immunology
Spleen/immunology
T-Lymphocytes/immunology
p-Azobenzenearsonate/immunology
Chemicals
Epitopes
Isoantibodies
p-Azobenzenearsonate
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sy M S
Bach B A
Brown A
Nisonoff A
Benacerraf B
Greene M I
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