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  <contributors>
    <authors>
      <author>Gardell, Jennifer</author>
    </authors>
    <secondary-authors>
      <author>Parker, David</author>
    </secondary-authors>
  </contributors>
  <titles>
    <title>Directed delivery of CD40 ligand from helper T cells to antigen-presenting B cells</title>
    <translated-title/>
    <tertiary-title/>
  </titles>
  <periodical>
    <full-title/>
  </periodical>
  <alt-periodical>
    <full-title/>
    <abbr-1/>
  </alt-periodical>
  <pages/>
  <section/>
  <volume/>
  <number/>
  <keywords>
    <keyword>Antigen-Presenting Cells</keyword>
    <keyword>Immunological Synapses</keyword>
    <keyword>Exosomes</keyword>
    <keyword>CD40 Ligand</keyword>
    <keyword>T-Lymphocytes, Helper-Inducer</keyword>
  </keywords>
  <dates>
    <year>2015</year>
    <pub-dates>
      <date>2015</date>
    </pub-dates>
  </dates>
  <abstract>This dissertation presents my studies investigating the delivery of CD40 ligand (CD40L,  CD154) from helper T lymphocytes to antigen-presenting B lymphocytes. CD40L is a  type two transmembrane TNF superfamily cytokine made by T cells that engages CD40  on antigen-presenting cells, including B cells, initiating downstream signaling resulting in  B cell proliferation, differentiation, and antibody formation. Helper T cells can produce  CD40L de novo upon antigen-specific interactions, but they also have an intracellular  secretory compartment containing a small amount of preformed CD40L that is brought to  the T cell surface rapidly upon antigen recognition.</abstract>
  <pub-location>Oregon Health and Science University</pub-location>
  <publisher/>
  <issn/>
  <isbn/>
  <custom3/>
  <custom7/>
  <notes/>
  <work-type>Dissertation</work-type>
  <electronic-resource-num>10.6083/M41C1VTD</electronic-resource-num>
  <urls>
    <related-urls>
      <url>https://digitalcollections.ohsu.edu/record/2946/files/3718_etd.pdf</url>
    </related-urls>
  </urls>
  <language/>
</record>

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