دورية أكاديمية
The Role of Co-stimulatory/Co-inhibitory Signals in Graft-vs.-Host Disease.
العنوان: | The Role of Co-stimulatory/Co-inhibitory Signals in Graft-vs.-Host Disease. |
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المؤلفون: | Kumar S; Department of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States., Leigh ND; Department of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States., Cao X; Department of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.; Department of Microbiology and Immunology, Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD, United States. |
المصدر: | Frontiers in immunology [Front Immunol] 2018 Dec 21; Vol. 9, pp. 3003. Date of Electronic Publication: 2018 Dec 21 (Print Publication: 2018). |
نوع المنشور: | Journal Article; Research Support, N.I.H., Extramural; Review |
اللغة: | English |
بيانات الدورية: | Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: [Lausanne : Frontiers Research Foundation] |
مواضيع طبية MeSH: | Costimulatory and Inhibitory T-Cell Receptors/*metabolism , Graft vs Host Disease/*immunology , Hematopoietic Stem Cell Transplantation/*adverse effects , Signal Transduction/*immunology , T-Lymphocytes/*immunology, Clinical Trials as Topic ; Costimulatory and Inhibitory T-Cell Receptors/agonists ; Costimulatory and Inhibitory T-Cell Receptors/antagonists & inhibitors ; Costimulatory and Inhibitory T-Cell Receptors/immunology ; Graft vs Host Disease/therapy ; Graft vs Leukemia Effect/drug effects ; Graft vs Leukemia Effect/immunology ; Humans ; Immunologic Factors/pharmacology ; Immunologic Factors/therapeutic use ; Immunotherapy/methods ; Major Histocompatibility Complex/immunology ; Signal Transduction/drug effects ; T-Lymphocytes/drug effects ; T-Lymphocytes/metabolism ; Transplantation, Homologous/adverse effects ; Treatment Outcome |
مستخلص: | Allogeneic hematopoietic cell transplantation (allo-HCT) is an effective immunotherapeutic approach for various hematologic and immunologic ailments. Despite the beneficial impact of allo-HCT, its adverse effects cause severe health concerns. After transplantation, recognition of host cells as foreign entities by donor T cells induces graft-vs.-host disease (GVHD). Activation, proliferation and trafficking of donor T cells to target organs and tissues are critical steps in the pathogenesis of GVHD. T cell activation is a synergistic process of T cell receptor (TCR) recognition of major histocompatibility complex (MHC)-anchored antigen and co-stimulatory/co-inhibitory signaling in the presence of cytokines. Most of the currently used therapeutic regimens for GVHD are based on inhibiting the allogeneic T cell response or T-cell depletion (TCD). However, the immunosuppressive drugs and TCD hamper the therapeutic potential of allo-HCT, resulting in attenuated graft-vs.-leukemia (GVL) effect as well as increased vulnerability to infection. In view of the drawback of overbroad immunosuppression, co-stimulatory, and co-inhibitory molecules are plausible targets for selective modulation of T cell activation and function that can improve the effectiveness of allo-HCT. Therefore, this review collates existing knowledge of T cell co-stimulation and co-inhibition with current research that may have the potential to provide novel approaches to cure GVHD without sacrificing the beneficial effects of allo-HCT. |
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معلومات مُعتمدة: | R01 HL135325 United States HL NHLBI NIH HHS |
فهرسة مساهمة: | Keywords: T cells; allogeneic hematopoietic cell transplantation (allo-HCT); co-stimulation/co-inhibition; graft -vs.-leukemia (GVL) effect; graft-vs.-host disease (GVHD) |
المشرفين على المادة: | 0 (Costimulatory and Inhibitory T-Cell Receptors) 0 (Immunologic Factors) |
تواريخ الأحداث: | Date Created: 20190111 Date Completed: 20191025 Latest Revision: 20200403 |
رمز التحديث: | 20221213 |
مُعرف محوري في PubMed: | PMC6309815 |
DOI: | 10.3389/fimmu.2018.03003 |
PMID: | 30627129 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1664-3224 |
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DOI: | 10.3389/fimmu.2018.03003 |