[Modifications of immunoglobulin distribution at the surface of immunocytes resulting from experimental conditions].
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Biomedical subjects
Publications and source records attributed to S Avrameas.
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Specific immune precipitates dissolve in concentrated solutions of alkali-metal halides, and of alkaline-earth-metal halides and thiocyanates. The quantity of protein dissolved depends on the nature of the antigen-antibody system, on the proportion of the antigen in the precipitate, and on the avidity of the antibody. The extent of solubilization is a function of the temperature, of the volume of solution used and of the concentration of the ions in the solution, and also depends on the nature of these ions. The dissolving power of bivalent cations is greater than that of monovalent ones, and is as follows: Mg(2+)[unk]Ba(2+)[unk]Ca(2+)[unk]Sr(2+). Antigen-antibody complexes and free antibodies, but no free antigen, are detected in supernatants of specific precipitates dissolved in solutions of electrolytes of low ionic strength. Antigen-antibody complexes, free antibodies and also free antigen are detected in supernatants of specific precipitates dissolved in solutions of electrolytes of high ionic strength. Comparable results are obtained when the electrolyte solutions are studied for their effect on the bonds formed between an antibody and its corresponding immunosorbent. Moreover, in the latter case, 50% of the fixed antibodies could be recovered by elution with distilled water.
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Antibody to horseradish peroxidase was localized by electron microscopic immunocytochemistry in cells of the popliteal lymph nodes of the rabbit after a single injection of antigen with complete Freund's adjuvant and after a second antigen administration. Synthesis of antibody, chiefly of 7S type, occurred simultaneously in two types of cells: large, clear, fixed, typical plasma cells, and small, dense, circulating cells which exhibit morphological characteristics of both small lymphocytes and plasma cells. We call the latter "lymphoplasmacytes" and propose that they arise from small lymphocytes. They secrete antibody by clasmatosis and continue to develop an elaborate endoplasmic reticulum after specific antibody synthesis ceases. In the presence of an additional antigenic stimulation, a second cycle of antibody synthesis may begin around the nucleus in the same cell, with antibody accumulating in the perinuclear space sometimes even before the previously synthesized antibody has been entirely secreted at the cell periphery. On this basis, we propose that the lymphoplasmacyte is a memory cell and that memory and antibody synthesis are two different activities of the same cell. The appearance of a small amount of 19S antibody may be correlated with the presence of a small number of antibody-containing, large lymphocytes.
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