Cellular transfer of autoimmune aspermogenic orchiepididymitis (AIAO) by the i.v. route in the guinea pig
In this study, AIAO was adoptively transferred with a high proportion of success to syngeneic recipient guinea pigs. Donors of strains 2 and 13 were sensitized with a series of spermatozoal autoantigens (whole spermatozoa and three autoantigens isolated therefrom: S, P and T). Syngeneic (experimenta...
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Veröffentlicht in: | Clinical and experimental immunology 1985-03, Vol.59 (3), p.593-603 |
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description | In this study, AIAO was adoptively transferred with a high proportion of success to syngeneic recipient guinea pigs. Donors of strains 2 and 13 were sensitized with a series of spermatozoal autoantigens (whole spermatozoa and three autoantigens isolated therefrom: S, P and T). Syngeneic (experimental) and allogeneic (control) recipients were all transferred by strictly i.v. injections of lymphoid cells. The damage observed in testis and epididymis (mainly in the latter) was identical to, but milder than, that seen in active forms of AIAO. The incidence and severity of the disease were dependent on: the type of inducing antigen, S, T, P in order of decreasing efficiency; the length of immunization in donors, with increasingly serious lesions as periods ranged from 1 to 4 weeks; the presence or not of a complementary treatment of recipients with bacterial adjuvant enhancing the disease. Other parameters were less important, such as the strain 2 or 13 specificities, the amount of immunogen or the addition of peritoneal cells to lymph node cells. Skin hypersensitivity was concomitantly transferred to a large majority of isogenic recipients. But the incidence and severity of the disease showed only a partial correlation with Arthus type or delayed type responses to autoantigens. Thus guinea pig AIAO, already known to be transferable by immune sera (mainly anti-P and also anti-T) may also be transferred in physiological conditions by sensitized lymphoid cells (mainly anti-S and also anti-T). |
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L ; VOISIN, G. A</creator><creatorcontrib>TOULLET, F ; CHADENIER, F ; MAILLARD, J. L ; VOISIN, G. A</creatorcontrib><description>In this study, AIAO was adoptively transferred with a high proportion of success to syngeneic recipient guinea pigs. Donors of strains 2 and 13 were sensitized with a series of spermatozoal autoantigens (whole spermatozoa and three autoantigens isolated therefrom: S, P and T). Syngeneic (experimental) and allogeneic (control) recipients were all transferred by strictly i.v. injections of lymphoid cells. The damage observed in testis and epididymis (mainly in the latter) was identical to, but milder than, that seen in active forms of AIAO. The incidence and severity of the disease were dependent on: the type of inducing antigen, S, T, P in order of decreasing efficiency; the length of immunization in donors, with increasingly serious lesions as periods ranged from 1 to 4 weeks; the presence or not of a complementary treatment of recipients with bacterial adjuvant enhancing the disease. Other parameters were less important, such as the strain 2 or 13 specificities, the amount of immunogen or the addition of peritoneal cells to lymph node cells. Skin hypersensitivity was concomitantly transferred to a large majority of isogenic recipients. But the incidence and severity of the disease showed only a partial correlation with Arthus type or delayed type responses to autoantigens. Thus guinea pig AIAO, already known to be transferable by immune sera (mainly anti-P and also anti-T) may also be transferred in physiological conditions by sensitized lymphoid cells (mainly anti-S and also anti-T).</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>PMID: 3157515</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford: Blackwell</publisher><subject>Animals ; Arthus Reaction - immunology ; Autoantigens - immunology ; Autoimmune Diseases - immunology ; Biological and medical sciences ; Epididymitis - immunology ; Guinea Pigs ; Gynecology. Andrology. Obstetrics ; Hypersensitivity, Delayed - immunology ; Immunization, Passive ; Injections, Intravenous ; Lymphocytes - immunology ; Male ; Male genital diseases ; Medical sciences ; Non tumoral diseases ; Orchitis - immunology ; Spermatogenesis ; Spermatozoa - immunology</subject><ispartof>Clinical and experimental immunology, 1985-03, Vol.59 (3), p.593-603</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1576920/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1576920/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9096733$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3157515$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TOULLET, F</creatorcontrib><creatorcontrib>CHADENIER, F</creatorcontrib><creatorcontrib>MAILLARD, J. L</creatorcontrib><creatorcontrib>VOISIN, G. A</creatorcontrib><title>Cellular transfer of autoimmune aspermogenic orchiepididymitis (AIAO) by the i.v. route in the guinea pig</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>In this study, AIAO was adoptively transferred with a high proportion of success to syngeneic recipient guinea pigs. Donors of strains 2 and 13 were sensitized with a series of spermatozoal autoantigens (whole spermatozoa and three autoantigens isolated therefrom: S, P and T). Syngeneic (experimental) and allogeneic (control) recipients were all transferred by strictly i.v. injections of lymphoid cells. The damage observed in testis and epididymis (mainly in the latter) was identical to, but milder than, that seen in active forms of AIAO. The incidence and severity of the disease were dependent on: the type of inducing antigen, S, T, P in order of decreasing efficiency; the length of immunization in donors, with increasingly serious lesions as periods ranged from 1 to 4 weeks; the presence or not of a complementary treatment of recipients with bacterial adjuvant enhancing the disease. Other parameters were less important, such as the strain 2 or 13 specificities, the amount of immunogen or the addition of peritoneal cells to lymph node cells. Skin hypersensitivity was concomitantly transferred to a large majority of isogenic recipients. But the incidence and severity of the disease showed only a partial correlation with Arthus type or delayed type responses to autoantigens. Thus guinea pig AIAO, already known to be transferable by immune sera (mainly anti-P and also anti-T) may also be transferred in physiological conditions by sensitized lymphoid cells (mainly anti-S and also anti-T).</description><subject>Animals</subject><subject>Arthus Reaction - immunology</subject><subject>Autoantigens - immunology</subject><subject>Autoimmune Diseases - immunology</subject><subject>Biological and medical sciences</subject><subject>Epididymitis - immunology</subject><subject>Guinea Pigs</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hypersensitivity, Delayed - immunology</subject><subject>Immunization, Passive</subject><subject>Injections, Intravenous</subject><subject>Lymphocytes - immunology</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Medical sciences</subject><subject>Non tumoral diseases</subject><subject>Orchitis - immunology</subject><subject>Spermatogenesis</subject><subject>Spermatozoa - immunology</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF1LwzAUhoMoc05_gpALEb3oyEeTNjfCGH4MBrvR65KmaRdpm5o0g_17g5ahV-fjPec9nOcMzDHlLCEkFedgjhASicAovQRX3n_GknNOZmBGMcsYZnNg1rptQysdHJ3sfa0dtDWUYbSm60KvofSDdp1tdG8UtE7tjR5MZapjZ0bj4cNqs9o9wvIIx72GZnlYQmfDGNP-p9ME02sJB9Ncg4tatl7fTHEBPl6e39dvyXb3ulmvtslABBoTjDOa4YqTVGKBsVCpkkRWGBFaMqRTmWNaMaxzzhThPCs1Q4yonJUqzfK4vABPv75DKDtdKd3Hz9picKaT7lhYaYr_Sm_2RWMPRUTCBUHR4H4ycPYraD8WnfEqYpK9tsEXGUcRcU7i4O3fS6cTE9yo30269Eq2dQSsjD-NCSR4Rin9BmAag_w</recordid><startdate>19850301</startdate><enddate>19850301</enddate><creator>TOULLET, F</creator><creator>CHADENIER, F</creator><creator>MAILLARD, J. L</creator><creator>VOISIN, G. A</creator><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19850301</creationdate><title>Cellular transfer of autoimmune aspermogenic orchiepididymitis (AIAO) by the i.v. route in the guinea pig</title><author>TOULLET, F ; CHADENIER, F ; MAILLARD, J. L ; VOISIN, G. A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p290t-117371d624a19119c4ca2ad1023b50e4a813d51e865c2667be5052c85bc478173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Arthus Reaction - immunology</topic><topic>Autoantigens - immunology</topic><topic>Autoimmune Diseases - immunology</topic><topic>Biological and medical sciences</topic><topic>Epididymitis - immunology</topic><topic>Guinea Pigs</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hypersensitivity, Delayed - immunology</topic><topic>Immunization, Passive</topic><topic>Injections, Intravenous</topic><topic>Lymphocytes - immunology</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Medical sciences</topic><topic>Non tumoral diseases</topic><topic>Orchitis - immunology</topic><topic>Spermatogenesis</topic><topic>Spermatozoa - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TOULLET, F</creatorcontrib><creatorcontrib>CHADENIER, F</creatorcontrib><creatorcontrib>MAILLARD, J. L</creatorcontrib><creatorcontrib>VOISIN, G. A</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TOULLET, F</au><au>CHADENIER, F</au><au>MAILLARD, J. L</au><au>VOISIN, G. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular transfer of autoimmune aspermogenic orchiepididymitis (AIAO) by the i.v. route in the guinea pig</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>1985-03-01</date><risdate>1985</risdate><volume>59</volume><issue>3</issue><spage>593</spage><epage>603</epage><pages>593-603</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>In this study, AIAO was adoptively transferred with a high proportion of success to syngeneic recipient guinea pigs. Donors of strains 2 and 13 were sensitized with a series of spermatozoal autoantigens (whole spermatozoa and three autoantigens isolated therefrom: S, P and T). Syngeneic (experimental) and allogeneic (control) recipients were all transferred by strictly i.v. injections of lymphoid cells. The damage observed in testis and epididymis (mainly in the latter) was identical to, but milder than, that seen in active forms of AIAO. The incidence and severity of the disease were dependent on: the type of inducing antigen, S, T, P in order of decreasing efficiency; the length of immunization in donors, with increasingly serious lesions as periods ranged from 1 to 4 weeks; the presence or not of a complementary treatment of recipients with bacterial adjuvant enhancing the disease. Other parameters were less important, such as the strain 2 or 13 specificities, the amount of immunogen or the addition of peritoneal cells to lymph node cells. Skin hypersensitivity was concomitantly transferred to a large majority of isogenic recipients. But the incidence and severity of the disease showed only a partial correlation with Arthus type or delayed type responses to autoantigens. Thus guinea pig AIAO, already known to be transferable by immune sera (mainly anti-P and also anti-T) may also be transferred in physiological conditions by sensitized lymphoid cells (mainly anti-S and also anti-T).</abstract><cop>Oxford</cop><pub>Blackwell</pub><pmid>3157515</pmid><tpages>11</tpages></addata></record> |
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subjects | Animals Arthus Reaction - immunology Autoantigens - immunology Autoimmune Diseases - immunology Biological and medical sciences Epididymitis - immunology Guinea Pigs Gynecology. Andrology. Obstetrics Hypersensitivity, Delayed - immunology Immunization, Passive Injections, Intravenous Lymphocytes - immunology Male Male genital diseases Medical sciences Non tumoral diseases Orchitis - immunology Spermatogenesis Spermatozoa - immunology |
title | Cellular transfer of autoimmune aspermogenic orchiepididymitis (AIAO) by the i.v. route in the guinea pig |
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