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PMID: 6184435 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Antigen-specific suppression in genetic responder mice to L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT). Characterization of conventional and hybridoma-derived factors produced by suppressor T cells from mice injected as neonates with syngeneic GAT macrophages.

The Journal of experimental medicine ·Vol. 156 ·No. 6 ·1982-12-01 ·Pages 1691-710

Sorensen CM, Pierce CW

Abstract

Spleen cells from C57BL/10 mice injected with syngeneic B10 L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT)-pulsed macrophages (GAT-M phi) within 18 h of birth were unable to respond to soluble GAT, GAT-methylated bovine serum albumin, or B10 GAT-M phi as adults. Spleen cells from these neonatally treated mice responded at control levels to GAT presented in allogeneic M phi and to sheep erythrocytes. Partially purified T cells from these neonatally treated mice suppressed responses by syngeneic virgin, but not primed, spleen cells in an antigen-specific manner and acted during the early phases of the response. These responder GAT-specific suppressor T cells (GAT-TSR) were sensitive to anti-Thy-1 + C and 500-rad irradiation and have the phenotype Ly-1-2+, I-J+; GAT-TSR cells can only suppress responses by spleen cells syngeneic with the GAT-TSR cells at the I-J subregion of H-2. Restimulation of these Ts cells with syngeneic GAT-M phi induces an antigen-specific suppressor factor within the supernatant fluid. The factor, GAT-TsFR, is a glycoprotein with a molecular weight between 48,000 and 63,000, as determined by gel filtration chromatography using isotonic buffers; it bears serologically detectable determinants encoded by the I-J subregion of the H-2 complex, has an antigen-binding site for GAT and L-glutamic acid50-L-tyrosine50, and shares idiotypic determinants with anti-GAT antibodies. The presence of GAT-TsFR in the first 36 h of in vitro culture is required for significant suppression. Furthermore, only responses by spleen cell syngeneic with the cells producing GAT-TsFR at the I-J subregion are suppressed. The fusion of GAT-TsFR-producing cells with BW5147 resulted in generation of two hybridomas with properties and characteristics identical to those of the conventional GAT-TsFR with one exception: conventional and hybridoma 372.D6.5 GAT-TsFR only suppress responses by spleen cells of the I-Jb haplotype, whereas suppression mediated by the second hybridoma GAT-TsFR (372.B3.5) is genetically unrestricted. These hybridoma GAT-TsFR are compared with nonresponder GAT-Ts factor (GAT-TsF) and these responder and nonresponder GAT-TsF are considered in the context of suppressor pathways.

MeSH Terms
Animals Animals, Newborn Antibody-Producing Cells/immunology Epitopes/genetics Genes, MHC Class II Hemolytic Plaque Technique Hybridomas/immunology Lymphokines/analysis,biosynthesis,pharmacology Macrophages/immunology,transplantation Mice Mice, Inbred A Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA Peptides/genetics,immunology Polymers Suppressor Factors, Immunologic T-Lymphocytes, Regulatory/immunology
Chemicals
Epitopes Lymphokines Peptides Polymers Suppressor Factors, Immunologic GAT
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sorensen C M
Pierce C W
References (29)
29 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1982-12-01
Pages
1691-710
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2186880
Subset
IM
Grants
NIAID NIH HHS · AI-13915 · United States
NIAID NIH HHS · AI-15353 · United States
NIGMS NIH HHS · GM-07067 · United States
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