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      Correlation of Hsp70 Serum Levels with Gross Tumor Volume and Composition of Lymphocyte Subpopulations in Patients with Squamous Cell and Adeno Non-Small Cell Lung Cancer

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          Abstract

          Heat-shock protein 70 (Hsp70) is frequently found on the plasma membrane of a large number of malignant tumors including non-small cell lung cancer (NSCLC) and gets released into the blood circulation in lipid vesicles. On the one hand, a membrane (m)Hsp70-positive phenotype correlates with a high aggressiveness of the tumor; on the other hand, mHsp70 serves as a target for natural killer (NK) cells that had been pre-stimulated with Hsp70-peptide TKD plus low-dose interleukin-2 (TKD/IL-2). Following activation, NK cells show an up-regulated expression of activatory C-type lectin receptors, such as CD94/NKG2C, NKG2D, and natural cytotoxicity receptors (NCRs; NKp44, NKp46, and NKp30) and thereby gain the capacity to kill mHsp70-positive tumor cells. With respect to these results, the efficacy of ex vivo TKD/IL-2 stimulated, autologous NK cells is currently tested in a proof-of-concept phase II clinical trial in patients with squamous cell NSCLC after radiochemotherapy (RCT) at the TUM. Inclusion criteria are histological proven, non-resectable NSCLC in stage IIIA/IIIB, clinical responses to RCT and a mHsp70-positive tumor phenotype. The mHsp70 status is determined in the serum of patients using the lipHsp70 ELISA test, which enables the quantification of liposomal and free Hsp70. Squamous cell and adeno NSCLC patients had significantly higher serum Hsp70 levels than healthy controls. A significant correlation of serum Hsp70 levels with the gross tumor volume was shown for adeno and squamous cell NSCLC. However, significantly elevated ratios of activated CD69 +/CD94 + NK cells that are associated with low serum Hsp70 levels were observed only in patients with squamous cell lung cancer. These data might provide a first hint that squamous cell NSCLC is more immunogenic than adeno NSCLC.

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          Most cited references38

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          HLA-E binds to natural killer cell receptors CD94/NKG2A, B and C.

          The protein HLA-E is a non-classical major histocompatibility complex (MHC) molecule of limited sequence variability. Its expression on the cell surface is regulated by the binding of peptides derived from the signal sequence of some other MHC class I molecules. Here we report the identification of ligands for HLA-E. We constructed tetramers in which recombinant HLA-E and beta2-microglobulin were refolded with an MHC leader-sequence peptide, biotinylated, and conjugated to phycoerythrin-labelled Extravidin. This HLA-E tetramer bound to natural killer (NK) cells and a small subset of T cells from peripheral blood. On transfectants, the tetramer bound to the CD94/NKG2A, CD94/NKGK2B and CD94/NKG2C NK cell receptors, but did not bind to the immunoglobulin family of NK cell receptors (KIR). Surface expression of HLA-E was enough to protect target cells from lysis by CD94/NKG2A+ NK-cell clones. A subset of HLA class I alleles has been shown to inhibit killing by CD94/NKG2A+ NK-cell clones. Only the HLA alleles that possess a leader peptide capable of upregulating HLA-E surface expression confer resistance to NK-cell-mediated lysis, implying that their action is mediated by HLA-E, the predominant ligand for the NK cell inhibitory receptor CD94/NKG2A.
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            Molecular chaperones in cellular protein folding.

            F U Hartl (1996)
            The folding of many newly synthesized proteins in the cell depends on a set of conserved proteins known as molecular chaperones. These prevent the formation of misfolded protein structures, both under normal conditions and when cells are exposed to stresses such as high temperature. Significant progress has been made in the understanding of the ATP-dependent mechanisms used by the Hsp70 and chaperonin families of molecular chaperones, which can cooperate to assist in folding new polypeptide chains.
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              Diversity of gene expression in adenocarcinoma of the lung.

              The global gene expression profiles for 67 human lung tumors representing 56 patients were examined by using 24,000-element cDNA microarrays. Subdivision of the tumors based on gene expression patterns faithfully recapitulated morphological classification of the tumors into squamous, large cell, small cell, and adenocarcinoma. The gene expression patterns made possible the subclassification of adenocarcinoma into subgroups that correlated with the degree of tumor differentiation as well as patient survival. Gene expression analysis thus promises to extend and refine standard pathologic analysis.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                02 November 2015
                2015
                : 6
                : 556
                Affiliations
                [1] 1Department of Radiation Oncology, Klinikum rechts der Isar, Technische Universität München (TUM) , München, Germany
                [2] 2Department of Radiation Oncology, Martin Luther University Halle-Wittenberg , Halle (Saale), Germany
                [3] 3Department of Pathology, Klinikum rechts der Isar, Technische Universität München (TUM) , München, Germany
                [4] 4Department of Innovative Radiotherapy (iRT), Helmholtz Zentrum München , Oberschleißheim, Germany
                [5] 5Department of Radiation Sciences (DRS), Helmholtz Zentrum München , Oberschleißheim, Germany
                [6] 6Pulmonary Division, 1 Medizinische Klinik, Klinikum rechts der Isar, Technische Universität München (TUM) , München, Germany
                Author notes

                Edited by: Francisco Borrego, Cruces University Hospital, Spain

                Reviewed by: Catharina C. Gross, University Hospital Münster, Germany; Franz Rödel, Johann Wolfgang Goethe-University Frankfurt am Main, Germany

                *Correspondence: Gabriele Multhoff, gabriele.multhoff@ 123456tum.de

                Sophie Gunther and Christian Ostheimer have contributed equally to this work.

                Specialty section: This article was submitted to NK Cell Biology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2015.00556
                4629690
                26579130
                93717fc5-c5a9-40f7-98c9-a6494543ef77
                Copyright © 2015 Gunther, Ostheimer, Stangl, Specht, Mozes, Jesinghaus, Vordermark, Combs, Peltz, Jung and Multhoff.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 September 2015
                : 17 October 2015
                Page count
                Figures: 5, Tables: 3, Equations: 0, References: 47, Pages: 12, Words: 8617
                Funding
                Funded by: European Commission 10.13039/501100000780
                Award ID: 315963
                Funded by: Bundesministerium für Bildung und Forschung 10.13039/501100002347
                Award ID: Strahlenkompetenz 02NUK007E, 02NUK031B, Innovative Therapies 01GU0823, NSCLC 16GW0030
                Funded by: Deutsche Forschungsgemeinschaft 10.13039/501100001659
                Award ID: Cluster of Excellence Munich Centre for Advanced Photonics, SFB824/2, FUGG 95/980-1 FUGG, FUGG 411/37-1 FUGG
                Funded by: Wilhelm Sander-Stiftung 10.13039/100008672
                Award ID: FKZ 2007.123.2
                Categories
                Immunology
                Original Research

                Immunology
                biomarker,tumor markers,biological,heat-shock protein 70,nsclc,gross tumor volume,lymphocytes,immune responses

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