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The Journal of Immunology, 1971, 106: 454-466.
Copyright © 1971 by The American Association of Immunologists, Inc.

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Immunoferritin Study of the Distribution of HL.A Antigens on Human Blood Cells1

François M. Kourilsky, Danielle Silvestre, Jean Paul Levy, Jean Dausset, Marie Gabrielle Nicolai and Anna Senik

From the Departments of Immunologie des Tumeurs and Immunohématologie, Institut de Recherche sur les Leucémies et les Maladies du Sang, Hôpital Saint-Louis, Paris, France

Abstract

The localization and distribution of human histocompatibility antigens of the HL.A system was studied in the membranes of a variety of peripheral blood and bone marrow cells, using an indirect ferritin-labeled antibody technique. The distribution of specific HL.A ferritin labeling at the cell membrane was found to be discontinuous, forming "patches" similar to those described for H-2 antigens in mice with indirect immunoferritin methods. The importance of the HL.A labeling at the cell surface varied considerably according to the spectrum of specificity of the anti HL.A antisera used. The cell prolongations were never labeled. The HL.A antigens were localized on all nucleated cells studied, including lymphocytes, monocytes, polymorphonuclear leukocytes, granulocyte precursors, stem cells, erythroblasts, leukemic cells and cultured lymphoid cells. However the comparative evaluation of the labeling suggested that the concentration of HL.A antigens is much lower at the membrane of immature cells. HL.A antigens were never detected on mature erythrocytes, but are still present on reticulocytes. These results suggest a heterogeneity of the human cell membrane with regard to the HL.A antigenic expression, and important variations of the concentration of these antigens according to the cell type and degree of differentiation.

Footnotes

1 This work was supported by CNRS (Laboratoire Associé n°47), Ligue Nationale Française contre le Cancer, and Delegation Generale à la Recherche Scientifique et Technique (Action Concertée Transplantation).




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