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STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS

The composition of various isolated antibodies was determined by quantitative analyses for heavy chain subgroups and light chain types. Certain antibodies such as anti-tetanus toxoid and anti-A isoagglutinins were predominantly of the major γG1-type. However, a high preponderance of molecules of the...

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Autores principales: Yount, William J., Dorner, Marianne M., Kunkel, Henry G., Kabat, Elvin A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1968
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138455/
https://www.ncbi.nlm.nih.gov/pubmed/4169968
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author Yount, William J.
Dorner, Marianne M.
Kunkel, Henry G.
Kabat, Elvin A.
author_facet Yount, William J.
Dorner, Marianne M.
Kunkel, Henry G.
Kabat, Elvin A.
author_sort Yount, William J.
collection PubMed
description The composition of various isolated antibodies was determined by quantitative analyses for heavy chain subgroups and light chain types. Certain antibodies such as anti-tetanus toxoid and anti-A isoagglutinins were predominantly of the major γG1-type. However, a high preponderance of molecules of the minor γG2-subgroup was found for antibodies to dextran, levan, and teichoic acid. These findings explain some unusual features previously noted for anti-dextrans such as weak PCA reactions and lack of Gm antigens. Studies of several isolated antibodies from single heterozygous individuals showed a selective absence of genetic markers in certain antibodies and their presence in others. The "allelic exclusion" principle was clearly evident in the isolated antibodies of two different individuals. Large differences in the ratio of kappa to lambda light chains were observed for the same type of antibody from different individuals. Subfractionation of dextran antibodies by affinity for specific glycosidic linkage or combining site size produced marked changes in the ratios. The isomaltohexaose eluates of the dextran antibodies from two subjects were primarily kappa and the isomaltotriose eluates were predominantly lambda. The one anti-levan antibody studied was uniquely homogeneous, consisting exclusively of γG2-heavy chains and kappa light chains. By these criteria as well as others, it closely resembled myeloma proteins.
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spelling pubmed-21384552008-04-17 STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS Yount, William J. Dorner, Marianne M. Kunkel, Henry G. Kabat, Elvin A. J Exp Med Article The composition of various isolated antibodies was determined by quantitative analyses for heavy chain subgroups and light chain types. Certain antibodies such as anti-tetanus toxoid and anti-A isoagglutinins were predominantly of the major γG1-type. However, a high preponderance of molecules of the minor γG2-subgroup was found for antibodies to dextran, levan, and teichoic acid. These findings explain some unusual features previously noted for anti-dextrans such as weak PCA reactions and lack of Gm antigens. Studies of several isolated antibodies from single heterozygous individuals showed a selective absence of genetic markers in certain antibodies and their presence in others. The "allelic exclusion" principle was clearly evident in the isolated antibodies of two different individuals. Large differences in the ratio of kappa to lambda light chains were observed for the same type of antibody from different individuals. Subfractionation of dextran antibodies by affinity for specific glycosidic linkage or combining site size produced marked changes in the ratios. The isomaltohexaose eluates of the dextran antibodies from two subjects were primarily kappa and the isomaltotriose eluates were predominantly lambda. The one anti-levan antibody studied was uniquely homogeneous, consisting exclusively of γG2-heavy chains and kappa light chains. By these criteria as well as others, it closely resembled myeloma proteins. The Rockefeller University Press 1968-02-29 /pmc/articles/PMC2138455/ /pubmed/4169968 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
Yount, William J.
Dorner, Marianne M.
Kunkel, Henry G.
Kabat, Elvin A.
STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title_full STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title_fullStr STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title_full_unstemmed STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title_short STUDIES ON HUMAN ANTIBODIES : VI. SELECTIVE VARIATIONS IN SUBGROUP COMPOSITION AND GENETIC MARKERS
title_sort studies on human antibodies : vi. selective variations in subgroup composition and genetic markers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138455/
https://www.ncbi.nlm.nih.gov/pubmed/4169968
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