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Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation

The spleen T cells from mice immunized 6 days earlier with either chicken gamma globulin (CGG) or with donkey erythrocytes (DRC) were rosetted with CGG-coated sheep erythrocytes or with DRC. The immune rosettes (RFC) (antigen-binding cells) were separated from the bulk of nonrosette-forming cells (n...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1975
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189943/
https://www.ncbi.nlm.nih.gov/pubmed/51900
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description The spleen T cells from mice immunized 6 days earlier with either chicken gamma globulin (CGG) or with donkey erythrocytes (DRC) were rosetted with CGG-coated sheep erythrocytes or with DRC. The immune rosettes (RFC) (antigen-binding cells) were separated from the bulk of nonrosette-forming cells (non-RFC) by 1-g velocity sedimentation and the RFC and non-RFC tested for helper activity in cooperative antihapten responses in vitro. RFC or non-RFC were mixed with normal or hapten-primed spleen cells, challenged with the appropriate hapten- carrier conjugate and cultured for 4 days in Marbrook tissue cultures. The helping activity was quantitated from the numbers of antihapten antibody-producing cells generated per culture. The results show that specific helper cell activity could be selectively recovered in the immune rosette-forming cell population whereas the non-RFC population was depleted of help. These findings indicate that the helper T cells express specific antigen binding receptors.
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spelling pubmed-21899432008-04-17 Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation J Exp Med Articles The spleen T cells from mice immunized 6 days earlier with either chicken gamma globulin (CGG) or with donkey erythrocytes (DRC) were rosetted with CGG-coated sheep erythrocytes or with DRC. The immune rosettes (RFC) (antigen-binding cells) were separated from the bulk of nonrosette-forming cells (non-RFC) by 1-g velocity sedimentation and the RFC and non-RFC tested for helper activity in cooperative antihapten responses in vitro. RFC or non-RFC were mixed with normal or hapten-primed spleen cells, challenged with the appropriate hapten- carrier conjugate and cultured for 4 days in Marbrook tissue cultures. The helping activity was quantitated from the numbers of antihapten antibody-producing cells generated per culture. The results show that specific helper cell activity could be selectively recovered in the immune rosette-forming cell population whereas the non-RFC population was depleted of help. These findings indicate that the helper T cells express specific antigen binding receptors. The Rockefeller University Press 1975-10-01 /pmc/articles/PMC2189943/ /pubmed/51900 Text en 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 Articles
Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title_full Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title_fullStr Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title_full_unstemmed Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title_short Antigen-binding T cells as helper cells. Separation of helper cells by immune rosette formation
title_sort antigen-binding t cells as helper cells. separation of helper cells by immune rosette formation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189943/
https://www.ncbi.nlm.nih.gov/pubmed/51900