Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/3678
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dc.creatorHera, Antonio de la-
dc.creatorMarcos, Miguel A. R.-
dc.creatorToribio, María Luisa-
dc.creatorMárquez, Carlos-
dc.creatorGaspar, Maria Luisa-
dc.creatorMartínez-Alonso, Carlos-
dc.date2008-04-22T12:11:56Z-
dc.date2008-04-22T12:11:56Z-
dc.date1987-09-
dc.date.accessioned2017-01-31T01:03:03Z-
dc.date.available2017-01-31T01:03:03Z-
dc.identifierThe Journal of Experimental Medicine, Vol. 166, Septembre (1987), pp. 804-809-
dc.identifier0022-1007-
dc.identifierhttp://hdl.handle.net/10261/3678-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/3678-
dc.descriptionEl copyright pertenece a The Rockefeller University Press-
dc.descriptionDevelopmental analyses of B cell differentiation are consistent with the existence of at least two distinct lineages . Thus, adult bone marrow solely regenerates the commonest (Ly-1 -) lineage, while Ly-1 + B cells reconstitute the Ly-1 + B cell lineage (1). CBA/N mice carrying the X-linked immunodeficiency gene (xid) show a defective differentiation of B lymphocytes (2) . They lack all Ly-1 + B cells as well as the normally predominant subpopulation within the Ly-1 - lineage (3) . Functional studies (4) indicated that Ly-1 + B cells are responsible for the production of most of the autoantibodies, while those B cells in the Ly-1 - lineage participate in the conventional responses to "foreign" antigens. These observations may account for both the protection conferred against autoimmune disease, when the xid genetic defect is bred into lupus-prone strains, and the CBA/N mice unresponsiveness to many bacterial antigens (5, 6) . Administration of the immunosuppressant cyclosporine A (CsA) at the time of autologous bone marrow reconstitution results in systemic autoimmunity in CBA/N mice. Besides, these mice show a severe diminution, if not absence, of bone marrow pre-B cells, but increased amounts of activated B cells and autoantibodies (7). We have now studied the possibility that Ly-1 + B cell precursors may exist in CBA/N mice and report here experiments indicating that this is indeed the case-
dc.descriptionPeer reviewed-
dc.format392959 bytes-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherRockefeller University Press-
dc.rightsopenAccess-
dc.titleDevelopment of Ly-1+ B Cells in immunodeficient CBA/N mice-
dc.typeArtículo-
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