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      OMIP‐080: 29‐Color flow cytometry panel for comprehensive evaluation of NK and T cells reconstitution after hematopoietic stem cells transplantation

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      1 , 1 , 1 ,
      Cytometry
      John Wiley & Sons, Inc.

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          Abstract

          This 29‐color panel was developed and optimized for the monitoring of NK cell and T cell reconstitution in peripheral blood of patients after HSCT. We considered major post‐HSCT complications during the design, such as relapses, viral infections, and GvHD and identification of lymphocyte populations relevant to their resolution. The panel includes markers for all major NK cell and T cell subsets and analysis of their development and qualitative properties. In the NK cell compartment, we focus mainly on CD57 + NKG2C+ cells and the expression of activating (NKG2D, DNAM‐1) and inhibitory receptors (NKG2A, TIGIT). Another priority is the characterization of T cell reconstitution; therefore, we included detection of CD4+ RTEs based on CD45RA, CD62L, CD95, and CD31 as a marker of thymus function. Besides that, we also analyze the emergence and properties of major T cell populations with a particular interest in CD8, Th1, ThCTL, and Treg subsets. Overall, the panel allows for comprehensive analysis of the reconstituting immune system and identification of potential markers of immune cell dysfunction.

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          Most cited references44

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          Lag-3, Tim-3, and TIGIT: Co-inhibitory Receptors with Specialized Functions in Immune Regulation.

          Co-inhibitory receptors, such as CTLA-4 and PD-1, have an important role in regulating T cell responses and have proven to be effective targets in the setting of chronic diseases where constitutive co-inhibitory receptor expression on T cells dampens effector T cell responses. Unfortunately, many patients still fail to respond to therapies that target CTLA-4 and PD-1. The next wave of co-inhibitory receptor targets that are being explored in clinical trials include Lag-3, Tim-3, and TIGIT. These receptors, although they belong to the same class of receptors as PD-1 and CTLA-4, exhibit unique functions, especially at tissue sites where they regulate distinct aspects of immunity. Increased understanding of the specialized functions of these receptors will inform the rational application of therapies that target these receptors to the clinic.
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            The biology and functional importance of MAIT cells

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              Immune Reconstitution after Allogeneic Hematopoietic Stem Cell Transplantation

              The timely reconstitution and regain of function of a donor-derived immune system is of utmost importance for the recovery and long-term survival of patients after allogeneic hematopoietic stem cell transplantation (HSCT). Of note, new developments such as umbilical cord blood or haploidentical grafts were associated with prolonged immunodeficiency due to delayed immune reconstitution, raising the need for better understanding and enhancing the process of immune reconstitution and finding strategies to further optimize these transplant procedures. Immune reconstitution post-HSCT occurs in several phases, innate immunity being the first to regain function. The slow T cell reconstitution is regarded as primarily responsible for deleterious infections with latent viruses or fungi, occurrence of graft-versus-host disease, and relapse. Here we aim to summarize the major steps of the adaptive immune reconstitution and will discuss the importance of immune balance in patients after HSCT.
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                Author and article information

                Contributors
                jan.musil@uhkt.cz
                Journal
                Cytometry A
                Cytometry A
                10.1002/(ISSN)1552-4930
                CYTO
                Cytometry
                John Wiley & Sons, Inc. (Hoboken, USA )
                1552-4922
                1552-4930
                24 October 2021
                January 2022
                : 101
                : 1 ( doiID: 10.1002/cyto.a.v101.1 )
                : 21-26
                Affiliations
                [ 1 ] Department of Immunomonitoring and Flow Cytometry Institute of Hematology and Blood Transfusion Prague Czech Republic
                Author notes
                [*] [* ] Correspondence

                Jan Musil, Department of Immunomonitoring and Flow Cytometry, Institute of Hematology and Blood Transfusion, U Nemocnice 2094/1, 128 00 Prague, Czech Republic.

                Email: jan.musil@ 123456uhkt.cz

                Author information
                https://orcid.org/0000-0002-9378-5956
                Article
                CYTOA24510
                10.1002/cyto.a.24510
                9298022
                34693626
                9b0856ce-3222-4f6a-b6bc-3dc58c560bc5
                © 2021 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 22 September 2021
                : 12 March 2021
                : 30 September 2021
                Page count
                Figures: 1, Tables: 2, Pages: 6, Words: 4643
                Funding
                Funded by: European Regional Development Fund and the state budget of the Czech Republic, project AIIHHP
                Award ID: CZ.02.1.01/0.0/0.0/16_025/0007428 OP RDE MEYS
                Funded by: Ministerstvo Zdravotnictví Ceské Republiky , doi 10.13039/501100003243;
                Funded by: H CZ ‐ DRO (Institute of Hematology and Blood Tranfusion ‐ IHBT)
                Award ID: IN 00023736
                Categories
                Omip
                Omip
                Custom metadata
                2.0
                January 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:20.07.2022

                Cell biology
                Cell biology

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