Cargando…
IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS
The immunochemical specificity of antigen-induced inhibition of peritoneal exudate cell migration was studied in animals sensitized to chemically defined α,DNP(Lys)(18) peptides. It was shown that sensitized peritoneal exudate cells could discriminate between various DNP-oligolysines. Only immunogen...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1968
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138577/ https://www.ncbi.nlm.nih.gov/pubmed/5688081 |
_version_ | 1782143595801739264 |
---|---|
author | David, John R. Schlossman, Stuart F. |
author_facet | David, John R. Schlossman, Stuart F. |
author_sort | David, John R. |
collection | PubMed |
description | The immunochemical specificity of antigen-induced inhibition of peritoneal exudate cell migration was studied in animals sensitized to chemically defined α,DNP(Lys)(18) peptides. It was shown that sensitized peritoneal exudate cells could discriminate between various DNP-oligolysines. Only immunogenic members of the homologous series of α,DNP-L-lysines equal to or larger in size than the heptamer inhibited the migration of specifically sensitized peritoneal exudate cells. In contrast, nonimmunogenic α,DNP-L-lysines, a D-lysine containing stereoisomer of α,DNP L(Lys)(9) (α,DNP-L(4)DL(4)) and (Lys)(9)ε, DNP were not inhibitory to the migration of peritoneal exudate cells derived from animals immunized to α,DNP(Lys)(18). The exquisite specificity of the in vitro reaction of sensitized cells with antigen contrasts with the previously observed in vivo or in vitro specificity of anti-α,-DNP(Lys)(n) antibody, but parallels the specificity of the in vivo delayed or anamnestic response. These results suggest the presence of a still undefined but highly specific binding site, which functions as the cellular receptor for antigen on the sensitized lymphoid cell or on some "processing" cell. |
format | Text |
id | pubmed-2138577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1968 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21385772008-04-17 IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS David, John R. Schlossman, Stuart F. J Exp Med Article The immunochemical specificity of antigen-induced inhibition of peritoneal exudate cell migration was studied in animals sensitized to chemically defined α,DNP(Lys)(18) peptides. It was shown that sensitized peritoneal exudate cells could discriminate between various DNP-oligolysines. Only immunogenic members of the homologous series of α,DNP-L-lysines equal to or larger in size than the heptamer inhibited the migration of specifically sensitized peritoneal exudate cells. In contrast, nonimmunogenic α,DNP-L-lysines, a D-lysine containing stereoisomer of α,DNP L(Lys)(9) (α,DNP-L(4)DL(4)) and (Lys)(9)ε, DNP were not inhibitory to the migration of peritoneal exudate cells derived from animals immunized to α,DNP(Lys)(18). The exquisite specificity of the in vitro reaction of sensitized cells with antigen contrasts with the previously observed in vivo or in vitro specificity of anti-α,-DNP(Lys)(n) antibody, but parallels the specificity of the in vivo delayed or anamnestic response. These results suggest the presence of a still undefined but highly specific binding site, which functions as the cellular receptor for antigen on the sensitized lymphoid cell or on some "processing" cell. The Rockefeller University Press 1968-11-30 /pmc/articles/PMC2138577/ /pubmed/5688081 Text en Copyright © 1968 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article David, John R. Schlossman, Stuart F. IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title | IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title_full | IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title_fullStr | IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title_full_unstemmed | IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title_short | IMMUNOCHEMICAL STUDIES ON THE SPECIFICITY OF CELLULAR HYPERSENSITIVITY : THE IN VITRO INHIBITION OF PERITONEAL EXUDATE CELL MIGRATION BY CHEMICALLY DEFINED ANTIGENS |
title_sort | immunochemical studies on the specificity of cellular hypersensitivity : the in vitro inhibition of peritoneal exudate cell migration by chemically defined antigens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138577/ https://www.ncbi.nlm.nih.gov/pubmed/5688081 |
work_keys_str_mv | AT davidjohnr immunochemicalstudiesonthespecificityofcellularhypersensitivitytheinvitroinhibitionofperitonealexudatecellmigrationbychemicallydefinedantigens AT schlossmanstuartf immunochemicalstudiesonthespecificityofcellularhypersensitivitytheinvitroinhibitionofperitonealexudatecellmigrationbychemicallydefinedantigens |