1974PubMedOpen access

Development of lymphocyte populations in the human foetal thymus and spleen.

Anthony Hayward, G Ezer

Open full text 54 citations

Abstract

T and B lymphocytes in the human foetal thymus and spleen were studied to determine the distribution and degree of development which takes place before exposure to environmental antigens occurs. Tests applied were spontaneous and complement-dependent rosette formation and immunofluorescence to detect surface immunoglobulins. Most thymus lymphocytes were spontaneous rosette-forming cells: the percentage of these cells in the spleen was lower. Complement receptor lymphocytes (CRL) were found in the spleen but not the thymus, suggesting that these tissues contain lymphocytes of different origin. Lymphocytes with surface immuno-globulin (SIg lymphocytes) were more numerous in the spleen than the thymus. Analysis of class-specific heavy chain and light chain determinants suggests that some foetal B cells carry heavy chains of more than one class. A possible model for foetal B-cell development and its relationship to antigen drive is discussed.

About this research paper

What this paper is about

T and B lymphocytes in the human foetal thymus and spleen were studied to determine the distribution and degree of development which takes place before exposure to environmental antigens occurs. Tests applied were spontaneous and complement-dependent rosette formation and immunofluorescence to detect surface immunoglobulins. Most thymus lymphocytes were spontaneous rosette-forming cells: the percentage of these cells in the spleen was lower. Complement receptor lymphocytes (CRL) were found in the spleen but not the thymus, suggesting that these tissues contain lymphocytes of different origin. Lymphocytes with surface immuno-globulin (SIg lymphocytes) were more numerous in the spleen than the thymus. Analysis of class-specific heavy chain and light chain determinants suggests that some foetal B cells carry heavy chains of more than one class. A possible model for foetal B-cell development and its relationship to antigen drive is discussed.

Why it matters

OpenAlex reports 54 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

T and B lymphocytes in the human foetal thymus and spleen were studied to determine the distribution and degree of development which takes place before exposure to environmental antigens occurs. Tests applied were spontaneous and complement-dependent rosette formation and immunofluorescence to detect surface immunoglobulins. Most thymus lymphocytes were spontaneous rosette-forming cells: the percentage of these cells in the spleen was lower. Complement receptor lymphocytes (CRL) were found in the spleen but not the thymus, suggesting that these tissues contain lymphocytes of different origin. Lymphocytes with surface immuno-globulin (SIg lymphocytes) were more numerous in the spleen than the thymus. Analysis of class-specific heavy chain and light chain determinants suggests that some foetal B cells carry heavy chains of more than one class. A possible model for foetal B-cell development and its relationship to antigen drive is discussed.

Key concepts: Spleen, Biology, Immunology, Antibody, Antigen, Immunofluorescence, Lymphocyte, Surface Immunoglobulin

Related papers

Back to paper searchBrowse research topicsOriginal source
Development of lymphocyte populations in the human foetal thymus and spleen. — Research Paper | ScholarLens