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    <title>Logtenberg, T.</title>
    <link>http://repub.eur.nl/res/aut/755/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Subtractive isolation of phage-displayed single-chain antibodies to thymic stromal cells by using intact thymic fragments (Article)</title>
      <link>http://repub.eur.nl/res/pub/8670/</link>
      <pubDate>1997-01-01T00:00:00Z</pubDate>
      <description>In the murine thymus, the stroma forms microenvironments that control
          different steps in T cell development. To study the architecture of such
          microenvironments and more particularly the nature of communicative
          signals in lympho-stromal interaction during T cell development, we have
          employed the phage antibody display technology, with the specific aim of
          isolating thymic stromal cell-specific single-chain antibodies from a
          semisynthetic phage library. A subtractive approach using intact, mildly
          fixed thymic fragments as target tissue and lymphocytes as absorber cells
          generated monoclonal phages (MoPhabs) detecting subsets of murine thymic
          stromal cells. In the present paper we report on the reactivity of
          single-chain antibodies derived from three MoPhabs, TB4-4, TB4-20, and
          TB4-28. While TB4-4 and TB4-20 are both epithelium specific, TB4-28
          detects an epitope expressed on both epithelial- and mesenchymal-derived
          stromal cells. TB4-4 reacts with all cortical epithelial cells and with
          other endoderm-derived epithelia, but this reagent leaves the majority of
          medullary epithelial cells unstained. In contrast, MoPhab TB4-20 detects
          both cortical and medullary thymic epithelial cells, as well as other
          endoderm- and ectoderm-derived epithelial cells. Cross-reaction of
          single-chain antibodies to human thymic stromal cells shows that our
          semisynthetic phage antibody display library, in combination with the
          present subtractive approach, permits detection of evolutionary conserved
          epitopes expressed on subsets of thymic stromal cells.</description>
    </item> <item>
      <title>Analysis of the antigen- and mitogen-induced differentiation of B lymphocytes from asymptomatic human immunodeficiency virus-seropositive male homosexuals. Discrepancy between T cell-dependent and T cell-independent activation. (Article)</title>
      <link>http://repub.eur.nl/res/pub/3325/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description>Five asymptomatic human immunodeficiency virus (HIV)-seropositive ; male homosexuals were immunized with the recall antigens tetanus toxoid (TT) and the three types of poliovirus present in diphtheria, tetanus, and polio vaccine. Four weeks after immunization, the in vivo response to booster immunization, the in vitro pokeweed mitogen (PWM)-induced IgG secretion, and the in vitro T cell-dependent and T cell-independent antigen-induced antibody response were assayed. Increase in serum antibody titer to TT and poliovirus was low and normal, respectively. In all five subjects studied, a high rate of spontaneous IgG production, including antibodies directed toward HIV was observed. Addition of PWM to the cultures induced suppression of the spontaneous IgG secretion. Only one donor showed a slightly increased IgG production after stimulation with PWM. Peripheral blood mononuclear cells of four of the five HIV-seropositive individuals did not produce TT, or poliovirus-specific antibodies when stimulated with the respective T cell-dependent antigens. However, stimulation of these peripheral blood mononuclear cells with TT coupled to agarose beads, which was shown to be T cell-independent, resulted in the generation of IgG anti-TT antibody-forming cells.</description>
    </item> <item>
      <title>Human peripheral blood lymphocytes from recently vaccinated individuals produce both type-specific and intertypic cross-reacting neutralizing antibody on in vitro stimulation with one type of poliovirus. (Article)</title>
      <link>http://repub.eur.nl/res/pub/3302/</link>
      <pubDate>1985-01-01T00:00:00Z</pubDate>
      <description>An in vitro system of poliovirus-specific antibody production by peripheral blood B cells on stimulation by the virus has been developed. Virus-neutralizing antibodies in culture supernatant fluids, or virus-specific antibody-secreting cells (ASC) were detected by microneutralization assay and ELISA-SPOT test, respectively. After booster immunization with polio vaccine, anti-poliovirus-neutralizing ASC were present in circulation. This response was measurable between 5 and 12 days after booster vaccination. At between 12 and 90 days, another subset of B cells was found in peripheral blood that only produced poliovirus-specific neutralizing antibody after in vitro antigenic stimulation. The in vitro virus-induced response required B cells, monocytes, and T4+ (T helper) cells, and was shown to result from de novo protein synthesis. The anti-poliovirus-neutralizing response in vitro could be dissected in a type-specific and intertypic cross-reactive response by using various antigen concentrations for in vitro stimulation. Evidence was obtained by absorption studies for the existence of intertypic cross-reactive neutralization-inducing epitopes.</description>
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