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dc.contributor.authorQI, Huibin
dc.contributor.authorTuzun, Erdem
dc.contributor.authorCHRISTADOSS, Premkumar
dc.contributor.authorLI, Jing
dc.contributor.authorALLMAN, Windy
dc.contributor.authorSAINI, Shamsher S.
dc.date.accessioned2021-03-05T08:09:56Z
dc.date.available2021-03-05T08:09:56Z
dc.identifier.citationALLMAN W., QI H., SAINI S. S. , LI J., Tuzun E., CHRISTADOSS P., "CD4 costimulation is not required in a novel LPS-enhanced model of myasthenia gravis", JOURNAL OF NEUROIMMUNOLOGY, cilt.249, ss.1-7, 2012
dc.identifier.issn0165-5728
dc.identifier.otherav_97788b33-244c-4d79-9a52-bbb04a14fb3b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101959
dc.identifier.urihttps://doi.org/10.1016/j.jneuroim.2012.04.002
dc.description.abstractThe potential of lipopolysaccharide (LPS) to induce antigen-specific B cell responses to acetylcholine receptor (AChR) in myasthenia gravis (MG) was evaluated in wild type (WT) and CD4-/- C57BL/6 mice. The WT mice immunized with AChR in LPS developed an MG-like disease (LPS-EAMG) similar to that induced by immunization with AChR in complete Freund's adjuvant (CFA-EAMG). CD4-/- mice were resistant to CFA-EAMG but susceptible to LPS-EAMG. LPS abrogated EAMG resistance in CD4-/- mice by increasing high-affinity anti-AChR IgG2b in sera and enhancing immune complex deposition in muscle. (C) 2012 Elsevier B.V. All rights reserved.
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectİmmünoloji
dc.titleCD4 costimulation is not required in a novel LPS-enhanced model of myasthenia gravis
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROIMMUNOLOGY
dc.contributor.departmentUniversity of Texas System , ,
dc.identifier.volume249
dc.identifier.startpage1
dc.identifier.endpage7
dc.contributor.firstauthorID2345


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