Presentation of anti-idiotypic antibody is sensitive to ionizing radiation
We have been investigating the generation of specific immune responses using monoclonal anti-idiotypic Abs (Ab2) as surrogate tumor Ag. We have prepared a series of idiotypic mAbs (Ab1) from CBH/cbi rats bearing the syngeneic sarcoma HSN and have used these Ab1 to generate autologous Ab2. By using t...
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Veröffentlicht in: | The Journal of immunology (1950) 1994-07, Vol.153 (2), p.574-583 |
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description | We have been investigating the generation of specific immune responses using monoclonal anti-idiotypic Abs (Ab2) as surrogate tumor Ag. We have prepared a series of idiotypic mAbs (Ab1) from CBH/cbi rats bearing the syngeneic sarcoma HSN and have used these Ab1 to generate autologous Ab2. By using the autologous Ab2 as Ag, we have isolated T cell lines from CBH/cbi rats that proliferate specifically in the presence of the Ab2, with spleen cells as APC. Specific proliferation of the T cells was prevented if the spleen cells used for presentation were irradiated with conventional doses of x-rays (1000 rad) just before use. Titration of the radiation response showed that the capacity of the spleen cells to present Ag decreased exponentially with x-ray doses of up to 100 rad, at which dose presentation was virtually abolished. The same irradiated spleen cells were fully competent to present OVA to CBH/cbi-derived rat T cell lines specific for this Ag. Preincubating the APC with Ag before irradiation abrogated the effect of x-irradiation on the presentation of Ab2. We conclude that, in this rat system, the presentation of autologous Ab2 is highly sensitive to the effects of low doses of x-rays. The clinical significance of these findings is discussed. |
doi_str_mv | 10.4049/jimmunol.153.2.574 |
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We have prepared a series of idiotypic mAbs (Ab1) from CBH/cbi rats bearing the syngeneic sarcoma HSN and have used these Ab1 to generate autologous Ab2. By using the autologous Ab2 as Ag, we have isolated T cell lines from CBH/cbi rats that proliferate specifically in the presence of the Ab2, with spleen cells as APC. Specific proliferation of the T cells was prevented if the spleen cells used for presentation were irradiated with conventional doses of x-rays (1000 rad) just before use. Titration of the radiation response showed that the capacity of the spleen cells to present Ag decreased exponentially with x-ray doses of up to 100 rad, at which dose presentation was virtually abolished. The same irradiated spleen cells were fully competent to present OVA to CBH/cbi-derived rat T cell lines specific for this Ag. Preincubating the APC with Ag before irradiation abrogated the effect of x-irradiation on the presentation of Ab2. We conclude that, in this rat system, the presentation of autologous Ab2 is highly sensitive to the effects of low doses of x-rays. The clinical significance of these findings is discussed.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.153.2.574</identifier><identifier>PMID: 8021496</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>ANIMAL CELLS ; Animals ; Antibodies, Anti-Idiotypic - immunology ; ANTIGEN-ANTIBODY REACTIONS ; Antigen-Presenting Cells - physiology ; BIOLOGICAL EFFECTS ; BIOLOGICAL MATERIALS ; BIOLOGICAL RADIATION EFFECTS ; BLOOD ; BLOOD CELLS ; BODY FLUIDS ; CONNECTIVE TISSUE CELLS ; ELECTROMAGNETIC RADIATION ; Female ; IMMUNE REACTIONS ; IONIZING RADIATIONS ; LEUKOCYTES ; Lymphatic Irradiation ; Lymphocyte Activation ; LYMPHOCYTES ; Male ; MATERIALS ; Mice ; RADIATION EFFECTS ; Radiation Tolerance ; RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT ; RADIATIONS ; Rats ; SOMATIC CELLS 560120 -- Radiation Effects on Biochemicals, Cells, & Tissue Culture ; SPLEEN CELLS ; T-Lymphocytes - immunology ; X RADIATION ; X-Rays</subject><ispartof>The Journal of immunology (1950), 1994-07, Vol.153 (2), p.574-583</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3464-cabc5df8b2e538f4aad1e18ed84d12e5b7625df881aad2cacc9df49e3de977aa3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8021496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/6936675$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnson-Leger, CA</creatorcontrib><creatorcontrib>Dean, CJ</creatorcontrib><title>Presentation of anti-idiotypic antibody is sensitive to ionizing radiation</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>We have been investigating the generation of specific immune responses using monoclonal anti-idiotypic Abs (Ab2) as surrogate tumor Ag. We have prepared a series of idiotypic mAbs (Ab1) from CBH/cbi rats bearing the syngeneic sarcoma HSN and have used these Ab1 to generate autologous Ab2. By using the autologous Ab2 as Ag, we have isolated T cell lines from CBH/cbi rats that proliferate specifically in the presence of the Ab2, with spleen cells as APC. Specific proliferation of the T cells was prevented if the spleen cells used for presentation were irradiated with conventional doses of x-rays (1000 rad) just before use. Titration of the radiation response showed that the capacity of the spleen cells to present Ag decreased exponentially with x-ray doses of up to 100 rad, at which dose presentation was virtually abolished. The same irradiated spleen cells were fully competent to present OVA to CBH/cbi-derived rat T cell lines specific for this Ag. Preincubating the APC with Ag before irradiation abrogated the effect of x-irradiation on the presentation of Ab2. We conclude that, in this rat system, the presentation of autologous Ab2 is highly sensitive to the effects of low doses of x-rays. The clinical significance of these findings is discussed.</description><subject>ANIMAL CELLS</subject><subject>Animals</subject><subject>Antibodies, Anti-Idiotypic - immunology</subject><subject>ANTIGEN-ANTIBODY REACTIONS</subject><subject>Antigen-Presenting Cells - physiology</subject><subject>BIOLOGICAL EFFECTS</subject><subject>BIOLOGICAL MATERIALS</subject><subject>BIOLOGICAL RADIATION EFFECTS</subject><subject>BLOOD</subject><subject>BLOOD CELLS</subject><subject>BODY FLUIDS</subject><subject>CONNECTIVE TISSUE CELLS</subject><subject>ELECTROMAGNETIC RADIATION</subject><subject>Female</subject><subject>IMMUNE REACTIONS</subject><subject>IONIZING RADIATIONS</subject><subject>LEUKOCYTES</subject><subject>Lymphatic Irradiation</subject><subject>Lymphocyte Activation</subject><subject>LYMPHOCYTES</subject><subject>Male</subject><subject>MATERIALS</subject><subject>Mice</subject><subject>RADIATION EFFECTS</subject><subject>Radiation Tolerance</subject><subject>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</subject><subject>RADIATIONS</subject><subject>Rats</subject><subject>SOMATIC CELLS 560120 -- Radiation Effects on Biochemicals, Cells, & Tissue Culture</subject><subject>SPLEEN CELLS</subject><subject>T-Lymphocytes - immunology</subject><subject>X RADIATION</subject><subject>X-Rays</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1P3DAQhi0EguXjDyAhRRy4ZbEdfyRHhMpHhdQeytly7Ak7KImX2NvV9tfXsEs59jSamed9R5qXkHNG54KK5voVh2E1hn7OZDXnc6nFHpkxKWmpFFX7ZEYp5yXTSh-R4xhfKaWKcnFIDmvKmWjUjHz_OUGEMdmEYSxCV9gxYYkeQ9os0X20bfCbAmORuYgJf0ORQpFx_IPjSzFZjx_qU3LQ2T7C2a6ekOe7b79uH8qnH_ePtzdPpauEEqWzrZO-q1sOsqo7Ya1nwGrwtfAsz1qt-Pu-ZnnDnXWu8Z1ooPLQaG1tdUIut74hJjTRYQK3cGEcwSWjmkopLTN0tYWWU3hbQUxmwOig7-0IYRWNVlJLzul_QaYaJUStM8i3oJtCjBN0ZjnhYKeNYdS8x2E-4zA5DsNNjiOLLnbuq3YA_0-y-__X9QW-LNY4gYmD7ftMM7Ner7-M_gJpf5du</recordid><startdate>19940715</startdate><enddate>19940715</enddate><creator>Johnson-Leger, CA</creator><creator>Dean, CJ</creator><general>Am Assoc Immnol</general><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>7T5</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>19940715</creationdate><title>Presentation of anti-idiotypic antibody is sensitive to ionizing radiation</title><author>Johnson-Leger, CA ; Dean, CJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3464-cabc5df8b2e538f4aad1e18ed84d12e5b7625df881aad2cacc9df49e3de977aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ANIMAL CELLS</topic><topic>Animals</topic><topic>Antibodies, Anti-Idiotypic - immunology</topic><topic>ANTIGEN-ANTIBODY REACTIONS</topic><topic>Antigen-Presenting Cells - physiology</topic><topic>BIOLOGICAL EFFECTS</topic><topic>BIOLOGICAL MATERIALS</topic><topic>BIOLOGICAL RADIATION EFFECTS</topic><topic>BLOOD</topic><topic>BLOOD CELLS</topic><topic>BODY FLUIDS</topic><topic>CONNECTIVE TISSUE CELLS</topic><topic>ELECTROMAGNETIC RADIATION</topic><topic>Female</topic><topic>IMMUNE REACTIONS</topic><topic>IONIZING RADIATIONS</topic><topic>LEUKOCYTES</topic><topic>Lymphatic Irradiation</topic><topic>Lymphocyte Activation</topic><topic>LYMPHOCYTES</topic><topic>Male</topic><topic>MATERIALS</topic><topic>Mice</topic><topic>RADIATION EFFECTS</topic><topic>Radiation Tolerance</topic><topic>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</topic><topic>RADIATIONS</topic><topic>Rats</topic><topic>SOMATIC CELLS 560120 -- Radiation Effects on Biochemicals, Cells, & Tissue Culture</topic><topic>SPLEEN CELLS</topic><topic>T-Lymphocytes - immunology</topic><topic>X RADIATION</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnson-Leger, CA</creatorcontrib><creatorcontrib>Dean, CJ</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnson-Leger, CA</au><au>Dean, CJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presentation of anti-idiotypic antibody is sensitive to ionizing radiation</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1994-07-15</date><risdate>1994</risdate><volume>153</volume><issue>2</issue><spage>574</spage><epage>583</epage><pages>574-583</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>We have been investigating the generation of specific immune responses using monoclonal anti-idiotypic Abs (Ab2) as surrogate tumor Ag. We have prepared a series of idiotypic mAbs (Ab1) from CBH/cbi rats bearing the syngeneic sarcoma HSN and have used these Ab1 to generate autologous Ab2. By using the autologous Ab2 as Ag, we have isolated T cell lines from CBH/cbi rats that proliferate specifically in the presence of the Ab2, with spleen cells as APC. Specific proliferation of the T cells was prevented if the spleen cells used for presentation were irradiated with conventional doses of x-rays (1000 rad) just before use. Titration of the radiation response showed that the capacity of the spleen cells to present Ag decreased exponentially with x-ray doses of up to 100 rad, at which dose presentation was virtually abolished. The same irradiated spleen cells were fully competent to present OVA to CBH/cbi-derived rat T cell lines specific for this Ag. Preincubating the APC with Ag before irradiation abrogated the effect of x-irradiation on the presentation of Ab2. We conclude that, in this rat system, the presentation of autologous Ab2 is highly sensitive to the effects of low doses of x-rays. The clinical significance of these findings is discussed.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>8021496</pmid><doi>10.4049/jimmunol.153.2.574</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ANIMAL CELLS Animals Antibodies, Anti-Idiotypic - immunology ANTIGEN-ANTIBODY REACTIONS Antigen-Presenting Cells - physiology BIOLOGICAL EFFECTS BIOLOGICAL MATERIALS BIOLOGICAL RADIATION EFFECTS BLOOD BLOOD CELLS BODY FLUIDS CONNECTIVE TISSUE CELLS ELECTROMAGNETIC RADIATION Female IMMUNE REACTIONS IONIZING RADIATIONS LEUKOCYTES Lymphatic Irradiation Lymphocyte Activation LYMPHOCYTES Male MATERIALS Mice RADIATION EFFECTS Radiation Tolerance RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT RADIATIONS Rats SOMATIC CELLS 560120 -- Radiation Effects on Biochemicals, Cells, & Tissue Culture SPLEEN CELLS T-Lymphocytes - immunology X RADIATION X-Rays |
title | Presentation of anti-idiotypic antibody is sensitive to ionizing radiation |
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