{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/68236"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/68236","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Mechanisms of Immunosuppression in Murine Malaria","abstract":"An extract was prepared from Plasmodium berghei, NK65C strain, by disrupting P. berghei infected erythrocytes with a Parr bomb disruption cell. This extract was capable of reducing the anti-DNP and SRBC plaque forming cell response of mice intraperitoneally injected with the extract one day prior to immunization. The suppressive substance of this crude extract was precipitated with 50% saturated ammonium sulfate (SAS) but not with 33% SAS. Further purification of the suppressor factor was possible by means of gel filtration chromatography on Sephadex G-150 using sodium borate buffer containing 6M guanidine hydrochloride. The purified soluble suppressive factor was tentatively characterized as a small glycoprotein (M.W. 27,000 daltons), possessing isoelectric point of 7.00. The suppressor activity could be abrogated by proteolytic enzyme digestion but was not abolished by periodate oxidation. The purified suppressor substance did not reduce the PFC response to DNP-Ficoll, a T-independent antigen, but it was capable of reducing the T-dependent anti-DNP and anti-SRBC PFC responses in high dilution. The data obtained from these experiments suggested that B cells are not the target of suppression.","abstract_html":"An extract was prepared from Plasmodium berghei, NK65C strain, by disrupting P. berghei infected erythrocytes with a Parr bomb disruption cell. This extract was capable of reducing the anti-DNP and SRBC plaque forming cell response of mice intraperitoneally injected with the extract one day prior to immunization. The suppressive substance of this crude extract was precipitated with 50% saturated ammonium sulfate (SAS) but not with 33% SAS. Further purification of the suppressor factor was possible by means of gel filtration chromatography on Sephadex G-150 using sodium borate buffer containing 6M guanidine hydrochloride. The purified soluble suppressive factor was tentatively characterized as a small glycoprotein (M.W. 27,000 daltons), possessing isoelectric point of 7.00. The suppressor activity could be abrogated by proteolytic enzyme digestion but was not abolished by periodate oxidation. The purified suppressor substance did not reduce the PFC response to DNP-Ficoll, a T-independent antigen, but it was capable of reducing the T-dependent anti-DNP and anti-SRBC PFC responses in high dilution. The data obtained from these experiments suggested that B cells are not the target of suppression.","abstract_has_math":false,"creators":["Khansari, Nematollah"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Veterinary Medical Science","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014-12-14T13:28:24Z","date_published":"2014-12-14T13:28:24Z","updated_at":"2026-07-22T22:25:58Z","subjects":["Biology, Veterinary Science"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(UMI)AAI8114442"],"render_values":[{"text":"(UMI)AAI8114442","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/68236","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Khansari, Nematollah"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2014-12-14T13:28:24Z","10000-01-01","1981"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Veterinary Medical Science"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biology, Veterinary Science"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/68236","(UMI)AAI8114442"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["An extract was prepared from Plasmodium berghei, NK65C strain, by disrupting P. berghei infected erythrocytes with a Parr bomb disruption cell. This extract was capable of reducing the anti-DNP and SRBC plaque forming cell response of mice intraperitoneally injected with the extract one day prior to immunization. The suppressive substance of this crude extract was precipitated with 50% saturated ammonium sulfate (SAS) but not with 33% SAS. Further purification of the suppressor factor was possible by means of gel filtration chromatography on Sephadex G-150 using sodium borate buffer containing 6M guanidine hydrochloride. The purified soluble suppressive factor was tentatively characterized as a small glycoprotein (M.W. 27,000 daltons), possessing isoelectric point of 7.00. The suppressor activity could be abrogated by proteolytic enzyme digestion but was not abolished by periodate oxidation. The purified suppressor substance did not reduce the PFC response to DNP-Ficoll, a T-independent antigen, but it was capable of reducing the T-dependent anti-DNP and anti-SRBC PFC responses in high dilution. The data obtained from these experiments suggested that B cells are not the target of suppression.","Made available in DSpace on 2014-12-14T13:28:24Z (GMT). No. of bitstreams: 1 8114442.pdf: 3777052 bytes, checksum: 57427e20a9e1953b5d2c6bf56551ae5a (MD5) Previous issue date: 1981","Embargo set by: Seth Robbins for item 68414 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","105 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1981."]},{"key":"dc:title","label":"Title","values":["Mechanisms of Immunosuppression in Murine Malaria"]}]}],"canonical_facts":{"dc:creator":["Khansari, Nematollah"],"dc:date":["2014-12-14T13:28:24Z","10000-01-01","1981"],"dc:description":["An extract was prepared from Plasmodium berghei, NK65C strain, by disrupting P. berghei infected erythrocytes with a Parr bomb disruption cell. This extract was capable of reducing the anti-DNP and SRBC plaque forming cell response of mice intraperitoneally injected with the extract one day prior to immunization. The suppressive substance of this crude extract was precipitated with 50% saturated ammonium sulfate (SAS) but not with 33% SAS. Further purification of the suppressor factor was possible by means of gel filtration chromatography on Sephadex G-150 using sodium borate buffer containing 6M guanidine hydrochloride. The purified soluble suppressive factor was tentatively characterized as a small glycoprotein (M.W. 27,000 daltons), possessing isoelectric point of 7.00. The suppressor activity could be abrogated by proteolytic enzyme digestion but was not abolished by periodate oxidation. The purified suppressor substance did not reduce the PFC response to DNP-Ficoll, a T-independent antigen, but it was capable of reducing the T-dependent anti-DNP and anti-SRBC PFC responses in high dilution. 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