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        <identifier>oai:www.ideals.illinois.edu:2142/20750</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_16456</setSpec>
        <setSpec>com_2142_5130</setSpec>
        <setSpec>com_2142_689</setSpec>
        <setSpec>com_2142_397</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:subject>Health Sciences, Nutrition</dc:subject>
          <dc:subject>Health Sciences, Immunology</dc:subject>
          <dc:contributor>Klein, Barbara P.</dc:contributor>
          <dc:creator>Liao, C. Hua</dc:creator>
          <dc:date>2011-05-07T12:48:11Z</dc:date>
          <dc:date>2011-05-07T12:48:11Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1993</dc:date>
          <dc:description>The objectives of the present study were to investigate the effects of vitamin A deficiency on the onset and progression of systemic lupus erythematosus (SLE), using the murine model, MRL/MPJ-lpr/lpr (MRL/l) mice in comparison with MRL/MP-+/+ (+/+) mice, and to postulate a possible mechanism. In Study I, sixty weanling female four week old MRL/l mice were randomly assigned to either the vitamin A-deficient (A-), A-sufficient (A+), and A-sufficient diet/feed restricted (DR) groups. In Study II fifty-eight same-age and -sex MRL/l mice were randomly assigned to either the A$-$ or A+ groups, while twenty-four +/+ mice, of the same sex and age range as MRL/l, were assigned to the normal control group (+/+ group). The results of both studies showed that vitamin A deficiency had a significant effect on preventing the MRL/l mice body weight loss due to the progression of SLE. Vitamin A deficiency also tended to suppress the abnormal enlargement of the thymus and spleen due to massive proliferation of abnormal T cells in MRL/l mice. The results of in vitro splenocyte proliferation tests indicate that vitamin A deficiency decreased the proportion of abnormal T and hypersecreation B cells so that the normal T and B cell ratio increased and was closer to the +/+ group in MRL/l mice. The results from Study II strongly suggested that the above beneficial effects of vitamin A deficiency were related to an increased expression of interleukin-2 (IL-2) receptor on the surface of the MRL/l mouse splenocytes, which resulted in an increased proliferation of normal T and B cells. To summarize, vitamin A deficiency decreases the overall progression of SLE in MRL/l mice. The mechanism includes an increased activity of suppressor T cells and an increased expression of IL-2 receptors on the surface of the splenocytes.</dc:description>
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  Previous issue date: 1993</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:46:01Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:20:30-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>AAI9314904</dc:identifier>
          <dc:identifier>(UMI)AAI9314904</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/20750</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1993 Liao, C. Hua</dc:rights>
          <dc:subject>Biology, Cell</dc:subject>
          <dc:title>The effects of vitamin A deficiency on the immune system in a murine model of systemic lupus erythematosus</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Human and Community Development</department>
            <discipline>Human and Community Development</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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