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dc.contributor.advisorChen, Wanjun
dc.contributor.authorCook, Melissa A.
dc.date.accessioned2011-10-20T18:10:38Z
dc.date.available2011-10-20T18:10:38Z
dc.date.issued1998
dc.identifier.urihttp://hdl.handle.net/10920/23716
dc.descriptionvii, 31 p.en_US
dc.description.abstractInjection of Group A streptococcal cell wall (SCW) peptidoglycan-polysaccharide complexes in susceptible rats induces acute inflammation in the joints followed by chronic arthritis, producing an attractive animal model for rheumatoid arthritis. Infiltration of neutrophils into the synovium characterizes the acute phase while accumulation of T cells and monocytes mediates the chronic phase. In this study, we first investigated the role of CD4+ and CD8+ T cells in the evolution of SCW-induced arthritis by in vivo immuno-deletion of these cells. We found that neither CD4+ nor CD8+ T cells affected acute inflammation. In contrast, both CD4 + and CD8+ T cells, at least in part, regulated the chronic response. Unexpectedly, CD8+ T cells played a more important role in the chronic phase because their deletion caused a dramatic increase in IL-4, an anti-inflammatory cytokine. Importantly, oral administration of SCW is known to suppress SCW induced arthritis in a dose dependent manner, however, the cells involved in oral tolerance are ill defined. As our second objective, we assessed the same in vivo immuno-deletion of CD4+ and CD8+ T cells. In orally tolerized animals, both CD4+ and CD8+ immuno-deletion resulted in an increase in the acute response, but only a partially resolved chronic inflammation. Immunohistochemical staining revealed that TGF-~, an anti-inflammatory cytokine, was markedly increased in the orally tolerized gut tissue, but not in the control animals. CD4+ and CD8+ immuno-deletion reduced the amount of TGF-𝛽 in the gut, compared to the tolerized animals. Therefore, our results demonstrated that both CD4+ and CD8+ T cells play an inhibitory role in acute inflammation in oral tolerance. In chronic inflammation, however, other factors may be important in helping CD4+ or CD8+ T cells maintain tolerance.en_US
dc.description.abstractWith honors.
dc.description.sponsorshipNational Institute of Dental Research. National Institutes of Health. Bethesda, Maryland.
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleThe role of CD4+ and CD8+ T cells in the Evolution of SCW Induced Arthritis and in Oral Toleranceen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


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  • Biology Senior Individualized Projects [1489]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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