Development of lymphocyte populations in the human foetal thymus and spleen.
Anthony Hayward, G Ezer
Abstract
Anthony Hayward, G Ezer
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.
OpenAlex reports 54 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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