<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-23T06:31:03Z</responseDate><request verb="GetRecord" identifier="oai:gupea.ub.gu.se:2077/56919" metadataPrefix="dim">https://gupea.ub.gu.se/server/oai/request</request><GetRecord><record><header><identifier>oai:gupea.ub.gu.se:2077/56919</identifier><datestamp>2018-11-13T02:33:56Z</datestamp><setSpec>com_2077_281</setSpec><setSpec>com_2077_17</setSpec><setSpec>com_2077_10556</setSpec><setSpec>col_2077_541</setSpec><setSpec>col_2077_310</setSpec><setSpec>col_2077_10557</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author">Hallner, Alexander</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2018-11-12T08:32:42Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2018-11-12T08:32:42Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2018-11-12</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="isbn">978-91-7833-201-4</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="isbn">978-91-7833-202-1</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/2077/56919</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="sv">Acute myeloid leukemia (AML) and chronic myelomonocytic leukemia (CMML) are potentially life-threatening blood cancers characterized by the expansion of malignant myeloid cells in bone marrow and other organs. This thesis aimed at contributing to the understanding of the role of natural killer (NK) cells in AML and CMML with focus on the potential impact of the immunosuppression exerted by reactive oxygen species (ROS) formed by the myeloid cell NOX2 enzyme. The thesis work has comprised in vitro studies of interactions between NK cells and primary myeloid leukemic cells along with analyses of NK cell repertoires in a clinical trial using a NOX2 inhibitor, histamine dihydrochloride (HDC) in conjunction with the NK cell-activating cytokine interleukin-2 (IL-2) for the prevention of relapse of AML after the completion of chemotherapy. Paper I reports that the functions and viability of cytotoxic lymphocytes, including NK cells, were compromised by ROS produced by leukemic myeloid cells recovered from patients with CMML. The results are thus suggestive of a novel mechanism of leukemia-induced immunosuppression in this disease. Paper II analyzed aspects of myeloid cell populations in AML using blood samples from a clinical phase IV trial where AML patients (n=84) received HDC in conjunction with IL-2. The results imply that HDC may exert anti-leukemic efficacy by facilitating the maturation of myeloid cells, which impacts on the efficiency of immunotherapy with HDC/IL-2. In papers III and IV we explored the role of killer cell immunoglobulin-like receptors (KIR) for the relapse and survival of AML patients receiving HDC/IL-2. The results suggest that a subset of immature NK cells with low KIR expression may determine clinical outcome. In paper IV we further analyzed results from the above-referenced phase IV trial and observed that a past cytomegalovirus (CMV) infection predicted high relapse risk and poor survival, presumably by reducing the pool of immature NK cells. The results of paper V suggest that a dimorphism in the leader peptide of HLA-B is relevant to NK cell-mediated killing of AML cells and to the outcome of immunotherapy. In conclusion, this thesis work presents novel aspects of myeloid cell-induced immunosuppression in AML and CMML and identifies NK cell subsets of potential relevance to the benefit of immunotherapy with HDC/IL-2.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="sv">eng</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="haspart" lang="sv">1. Aurelius J*, Hallner A*, Werlenius O, Riise R, Möllgård L, Brune M, Hansson M, Martner A, Thorén FB, Hellstrand K. NOX2‐dependent immunosuppression in chronic myelomonocytic leukemia. ::doi::10.1189/jlb.5VMA1116-454R</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="haspart" lang="sv">2. Rydström A*, Hallner A*, Aurelius J, Sander FE, Bernson E, Kiffin R, Thoren FB, Hellstrand K, Martner A. Dynamics of myeloid cell populations during relapse‐preventive immunotherapy in acute myeloid leukemia. ::doi::10.1189/jlb.5VMA1116-455R</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="haspart" lang="sv">3. Bernson E, Hallner A, Sander FE, Wilsson O, Werlenius O, Rydström A, Kiffin R, Brune M, Foà R, Aurelius J, Martner A, Hellstrand K, Thorén FB. Impact of killer-immunoglobulin-like receptor and human leukocyte antigen genotypes on the efficacy of immunotherapy in acute myeloid leukemia. ::doi::10.1038/leu.2017.151</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="haspart" lang="sv">4. Bernson E, Hallner A, Sander FE, Nicklasson M, Nilsson MS, Christenson K, Aydin E, Liljeqvist JÅ, Brune M, Foà R, Aurelius J, Martner A, Hellstrand K, Thorén FB.  Cytomegalovirus serostatus affects autoreactive NK cells and outcomes of IL2-based immunotherapy in acute myeloid leukemia. ::doi::10.1158/2326-6066.CIR-17-0711</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="haspart" lang="sv">5. Hallner A, Bernson E, Hussein BA, Sander FE, Brune M, Aurelius J, Martner A, Hellstrand K, Thorén FB The HLA-B -21 dimorphism impacts on NK cell education and clinical outcome of immunotherapy in acute myeloid leukemia</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">Natural killer cells</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">acute myeloid leukemia</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">histamine dihydrochloride</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">immunotherapy</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">reactive oxygen species</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">chronic myelomonocytic leukemia</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">NK cell education</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">NKG2A</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">HLA</dim:field>
   <dim:field mdschema="dc" element="subject" lang="sv">KIR</dim:field>
   <dim:field mdschema="dc" element="title" lang="sv">Immunotherapy and immunosuppression in myeloid leukemia</dim:field>
   <dim:field mdschema="dc" element="type" lang="eng">text</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="svep" lang="eng">Doctoral thesis</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="degree" lang="sv">Doctor of Philosophy (Medicine)</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="mail" lang="sv">alexander.hallner@gu.se</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="origin" lang="sv">University of Gothenburg. Sahlgrenska Academy</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="department" lang="sv">Institute of Biomedicine. Department of Infectious Diseases</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="defenceplace" lang="sv">Torsdagen den 29 november 2018, kl. 9:00, Hörsal Björn Folkow, Medicinaregatan 11, Göteborg</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="defencedate">2018-11-29</dim:field>
   <dim:field mdschema="dc" element="gup" qualifier="dissdb-fakultet">SA</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
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