In vivo kinetics and nature of rat IgE-bearing lymphocytes after IgE stimulation

Surface IgE-bearing (sIgE+) cells were studied in BN and rnu/rnu athymic rats after Nippostrongylus brasiliensis infection or i.p. injection of unpurified or purified IgE from plasmacytoma ascitic fluid. The number of sIgE+ cells increased markedly after a serum IgE increase without change in the pr...

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Veröffentlicht in:The Journal of immunology (1950) 1984-12, Vol.133 (6), p.3274-3281
Hauptverfasser: Manouvriez, P, Bazin, H
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description Surface IgE-bearing (sIgE+) cells were studied in BN and rnu/rnu athymic rats after Nippostrongylus brasiliensis infection or i.p. injection of unpurified or purified IgE from plasmacytoma ascitic fluid. The number of sIgE+ cells increased markedly after a serum IgE increase without change in the proportion of sIgM+ and sIgD+ cells. A high percentage of the sIgE+ cells bore cytophilic IgE. Receptors for IgE were induced with a 2.56-micrograms IgE injection/100 g body weight and reached a maximum with 1.6 mg IgE/100 g body weight. They appeared less than 4 hr after a single injection of purified IgE. The number of IgE receptor-bearing cells reached a maximum plateau at 24 hr to day 3 after injection and declined thereafter, to reach the control level on day 9 or 11 after injection. Nearly all the sIgE+ cells of BN rats also bore sIgD, but the number of triple sIgE-sIgM-sIgD+ cells varied in a wide range. Maximum 4.5% of the sIgE+ cells of euthymic rats were T cells. More than 98% of the sIgE+ cells of nude rats were triple sIgM-sIgD-sIgE+ cells, and the majority were cytophilic IgE+. For the most part, the sIgM-sIgD-sIgE+ cells are probably not cells that can differentiate, as generally accepted, in IgE-producing cells. New interpretations of the role of these triple sIgM-sIgD-sIgE+ cells in IgE immune responses are necessary.
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The number of sIgE+ cells increased markedly after a serum IgE increase without change in the proportion of sIgM+ and sIgD+ cells. A high percentage of the sIgE+ cells bore cytophilic IgE. Receptors for IgE were induced with a 2.56-micrograms IgE injection/100 g body weight and reached a maximum with 1.6 mg IgE/100 g body weight. They appeared less than 4 hr after a single injection of purified IgE. The number of IgE receptor-bearing cells reached a maximum plateau at 24 hr to day 3 after injection and declined thereafter, to reach the control level on day 9 or 11 after injection. Nearly all the sIgE+ cells of BN rats also bore sIgD, but the number of triple sIgE-sIgM-sIgD+ cells varied in a wide range. Maximum 4.5% of the sIgE+ cells of euthymic rats were T cells. More than 98% of the sIgE+ cells of nude rats were triple sIgM-sIgD-sIgE+ cells, and the majority were cytophilic IgE+. For the most part, the sIgM-sIgD-sIgE+ cells are probably not cells that can differentiate, as generally accepted, in IgE-producing cells. New interpretations of the role of these triple sIgM-sIgD-sIgE+ cells in IgE immune responses are necessary.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells</subject><subject>Cell interactions</subject><subject>Cytoplasm - immunology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Hookworm Infections - immunology</subject><subject>Immunobiology</subject><subject>Immunoglobulin E - administration &amp; dosage</subject><subject>Immunoglobulin E - metabolism</subject><subject>Immunoglobulin E - physiology</subject><subject>Kinetics</subject><subject>Leukocyte Count</subject><subject>Lymph Nodes - cytology</subject><subject>Lymphocytes - classification</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - metabolism</subject><subject>Male</subject><subject>Rats</subject><subject>Rats, Inbred BN</subject><subject>Rats, Mutant Strains</subject><subject>Receptors, Antigen, B-Cell - metabolism</subject><subject>Receptors, IgE</subject><subject>Receptors, Immunologic - analysis</subject><subject>Spleen - cytology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkM1qGzEUhUVISFy3TxACWoR2Na5-ZjTyMoS0NQSaRbsWd_RjK9FoHGkmxm9fGTuhaHEX57tH3A-ha0oWNamX3599309xCAvK-UIsOGvrMzSjTUMqIYg4RzNCGKtoK9or9CnnZ0KIIKy-RJeCcUmWYoaeVhG_-bcBv_hoR68zhmhwhHFKFg8OJxjxav1QdRaSj2sc9v12M-j9aAvpRpsOKc6j76cAox_iZ3ThIGT75TTn6O-Phz_3v6rH3z9X93ePleaM1pXh1gEpVzBNwGhJOmNrZ4zRRDDXGt7VTnaMUtNIqTsmKJW04a4xHQDhwOfo67F3m4bXyeZR9T5rGwJEO0xZScrLK3fOET-COg05J-vUNvke0l5Rog4e1btHVTwqoQ4ey9bNqX7qems-dk7iSn57yiFrCC5B1D5_YHIplpK2Bft2xDZ-vdn5ZFXuIYRSStVut_vvw3_BeouX</recordid><startdate>198412</startdate><enddate>198412</enddate><creator>Manouvriez, P</creator><creator>Bazin, H</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198412</creationdate><title>In vivo kinetics and nature of rat IgE-bearing lymphocytes after IgE stimulation</title><author>Manouvriez, P ; Bazin, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3214-d3efa00492c0adc80bde4fdddc062f7d3b4f8b211d588cb26118153f5dbaa03a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells</topic><topic>Cell interactions</topic><topic>Cytoplasm - immunology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Hookworm Infections - immunology</topic><topic>Immunobiology</topic><topic>Immunoglobulin E - administration &amp; dosage</topic><topic>Immunoglobulin E - metabolism</topic><topic>Immunoglobulin E - physiology</topic><topic>Kinetics</topic><topic>Leukocyte Count</topic><topic>Lymph Nodes - cytology</topic><topic>Lymphocytes - classification</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - metabolism</topic><topic>Male</topic><topic>Rats</topic><topic>Rats, Inbred BN</topic><topic>Rats, Mutant Strains</topic><topic>Receptors, Antigen, B-Cell - metabolism</topic><topic>Receptors, IgE</topic><topic>Receptors, Immunologic - analysis</topic><topic>Spleen - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Manouvriez, P</creatorcontrib><creatorcontrib>Bazin, H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Manouvriez, P</au><au>Bazin, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo kinetics and nature of rat IgE-bearing lymphocytes after IgE stimulation</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1984-12</date><risdate>1984</risdate><volume>133</volume><issue>6</issue><spage>3274</spage><epage>3281</epage><pages>3274-3281</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>Surface IgE-bearing (sIgE+) cells were studied in BN and rnu/rnu athymic rats after Nippostrongylus brasiliensis infection or i.p. injection of unpurified or purified IgE from plasmacytoma ascitic fluid. The number of sIgE+ cells increased markedly after a serum IgE increase without change in the proportion of sIgM+ and sIgD+ cells. A high percentage of the sIgE+ cells bore cytophilic IgE. Receptors for IgE were induced with a 2.56-micrograms IgE injection/100 g body weight and reached a maximum with 1.6 mg IgE/100 g body weight. They appeared less than 4 hr after a single injection of purified IgE. The number of IgE receptor-bearing cells reached a maximum plateau at 24 hr to day 3 after injection and declined thereafter, to reach the control level on day 9 or 11 after injection. Nearly all the sIgE+ cells of BN rats also bore sIgD, but the number of triple sIgE-sIgM-sIgD+ cells varied in a wide range. Maximum 4.5% of the sIgE+ cells of euthymic rats were T cells. More than 98% of the sIgE+ cells of nude rats were triple sIgM-sIgD-sIgE+ cells, and the majority were cytophilic IgE+. For the most part, the sIgM-sIgD-sIgE+ cells are probably not cells that can differentiate, as generally accepted, in IgE-producing cells. New interpretations of the role of these triple sIgM-sIgD-sIgE+ cells in IgE immune responses are necessary.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>6238096</pmid><doi>10.4049/jimmunol.133.6.3274</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Analysis of the immune response. Humoral and cellular immunity
Animals
Biological and medical sciences
Bone Marrow Cells
Cell interactions
Cytoplasm - immunology
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Hookworm Infections - immunology
Immunobiology
Immunoglobulin E - administration & dosage
Immunoglobulin E - metabolism
Immunoglobulin E - physiology
Kinetics
Leukocyte Count
Lymph Nodes - cytology
Lymphocytes - classification
Lymphocytes - immunology
Lymphocytes - metabolism
Male
Rats
Rats, Inbred BN
Rats, Mutant Strains
Receptors, Antigen, B-Cell - metabolism
Receptors, IgE
Receptors, Immunologic - analysis
Spleen - cytology
title In vivo kinetics and nature of rat IgE-bearing lymphocytes after IgE stimulation
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