Volume 17, Issue 9 pp. 1311-1316
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Newly produced virgin B cells migrate to secondary lymphoid organs but their capacity to enter follicles is restricted

Jennifer E. Lortan

Jennifer E. Lortan

Department of Immunology, University of Birmingham Medical School, Birmingham

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Carl A. Roobottom

Carl A. Roobottom

Department of Immunology, University of Birmingham Medical School, Birmingham

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Susan Oldfield

Susan Oldfield

Department of Immunology, University of Birmingham Medical School, Birmingham

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Ian C. M. MacLennan

Corresponding Author

Ian C. M. MacLennan

Department of Immunology, University of Birmingham Medical School, Birmingham

Department of Immunology, The Medical School, University of Birmingham, Birmingham B152TJ, GBSearch for more papers by this author
First published: 1987
Citations: 59

Abstract

The migration of recirculating B cells was compared with that of newly produced virgin B cells following passive cell transfer between congenic strains of rats differing in their kappa immunoglobulin light chain (χ) allotype. The number and location of donor B cells in the secondary lymphoid organs was determined at intervals following transfer by immunohistology using monoclonal antibodies specific for rat χ allotypes. Recirculating B cells were obtained from thoracic duct lymph while bone marrow from rats depleted of recirculating cells was used as a source of newly produced virgin B cells.

B cells from both sources gained immediate access to extrafollicular areas of secondary lymphoid organs rich in interdigitating cells and T cells. However, in lymph nodes extrafollicular B cells were found adjacent to lymphatics and not in the central paracortex. By 8 h after transfer most B cells from thoracic duct lymph were found in follicles. However, the capacity of the bone marrow B cells to enter follicles was very limited. These results are interpreted in relation to previous observations concerning (a) the timing of virgin B cell recruitment into T cell-dependent antibody responses, and (b) the role of B cells in antigen presentation.

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