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Phenotypic Profiles of Lymphocytes in Adult C57BL/6N Mice Infected With Cryptosporidium parvum

The purpose of this study was to quan ti tate the populations o f lymphocytes in the s pleens and intestines of normal and immunosuppressed adult C57BL/6N mice that were noninfected or infected with Cryptosporidi um parvum. This was accomplished by using the following methodologies: immunohistochemistry, ELISA-spot assay, and flow cytometry.
Mice in groups 1 and 2 were immunosuppressed, but only group 2 was in fected. Mice in group 3 were only infected, whereas group 4 served as the normal control . Mice were immunosuppressed with dexamethasone (DEXI at a dosage of 125~g / mouse/day. Infected mice received 106 oocysts per os . The numbers o f lymphocytes were monitored from day 0 to day 18 postinfect i on. Flow cytometry using antibodies directed against CD4+ and CDS+ T cells (helper and cytotoxic, respectively) and B cells (expressing IgG, IgM, and IgA receptors) revealed that c. parvum did not evoke an alteration in the phenotypic profile of lymphocytes within spleens or Peyer's patches (PP) of mice in groups 2 and 3 that was statist i cally different from groups 1 and 4. Immunosuppressed mice (groups 1 and 2) had significantly fewer lymphocytes (bearing CD4+, IgG, IgM, and IgA receptors) within the spleen when compared with mice in groups 3 and 4 (P

Identiferoai:union.ndltd.org:UTAHS/oai:digitalcommons.usu.edu:etd-4881
Date01 May 1994
CreatorsBienek, Diane Rose
PublisherDigitalCommons@USU
Source SetsUtah State University
Detected LanguageEnglish
Typetext
Formatapplication/pdf
SourceAll Graduate Theses and Dissertations
RightsCopyright for this work is held by the author. Transmission or reproduction of materials protected by copyright beyond that allowed by fair use requires the written permission of the copyright owners. Works not in the public domain cannot be commercially exploited without permission of the copyright owner. Responsibility for any use rests exclusively with the user. For more information contact Andrew Wesolek (andrew.wesolek@usu.edu).

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