Search Results - "Sitkovsky, Michail V."
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Immunological mechanisms of the antitumor effects of supplemental oxygenation
Published in Science translational medicine (04-03-2015)“…Antitumor T cells either avoid or are inhibited in hypoxic and extracellular adenosine-rich tumor microenvironments (TMEs) by A2A adenosine receptors. This may…”
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Hypoxia and hypoxia-inducible factor (HIF) downregulate antigen-presenting MHC class I molecules limiting tumor cell recognition by T cells
Published in PloS one (20-11-2017)“…Human cancers are known to downregulate Major Histocompatibility Complex (MHC) class I expression thereby escaping recognition and rejection by anti-tumor T…”
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Hypoxia-Adenosinergic Immunosuppression: Tumor Protection by T Regulatory Cells and Cancerous Tissue Hypoxia
Published in Clinical cancer research (01-10-2008)“…Cancerous tissue protection from tumor-recognizing CD8 + and CD4 + T cells (antitumor T cells) limits the therapeutic potential of immunotherapies. We propose…”
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Immunomodulatory and neuroprotective effects of inosine
Published in Trends in pharmacological sciences (Regular ed.) (01-03-2004)“…Adenosine has been considered as a potential immunomodulatory and neuroprotective agent for 30 years. Inosine, a major degradation product of adenosine, was…”
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Targeted Elimination of Immunodominant B Cells Drives the Germinal Center Reaction toward Subdominant Epitopes
Published in Cell reports (Cambridge) (26-12-2017)“…Rapidly evolving pathogens such as HIV or influenza can quickly mutate their antigenic profiles, reducing the efficacy of conventional vaccines. Despite this…”
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Oxygenation inhibits the physiological tissue-protecting mechanism and thereby exacerbates acute inflammatory lung injury
Published in PLoS biology (01-06-2005)“…Acute respiratory distress syndrome (ARDS) usually requires symptomatic supportive therapy by intubation and mechanical ventilation with the supplemental use…”
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Toll-like Receptor 3 Regulates Angiogenesis and Apoptosis in Prostate Cancer Cell Lines through Hypoxia-Inducible Factor 1α
Published in Neoplasia (New York, N.Y.) (01-07-2010)“…Toll-like receptors (TLRs) recognize microbial/viral-derived components that trigger innate immune response and conflicting data implicate TLR agonists in…”
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Differential requirement for A2a and A3 adenosine receptors for the protective effect of inosine in vivo
Published in Blood (15-12-2003)“…Inosine is an endogenous nucleoside with immunosuppressive properties that is known to inhibit the accumulation of proinflammatory cytokines and protect mice…”
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Mechanisms of Disease: Purinergic Signaling during Inflammation
Published in The New England journal of medicine (13-12-2012)“…Receptors for ATP and ADP and adenosine exert various effects. ATP and ADP signaling is mainly proinflammatory, and adenosine signaling is mainly…”
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Purinergic Signaling during Inflammation
Published in The New England journal of medicine (13-12-2012)“…Receptors for ATP and ADP and adenosine exert various effects. ATP and ADP signaling is mainly proinflammatory, and adenosine signaling is mainly…”
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Antihypoxic oxygenation agents with respiratory hyperoxia to improve cancer immunotherapy
Published in The Journal of clinical investigation (01-11-2020)“…Hypoxia/HIF-1α- and extracellular adenosine/A2 adenosine receptor-mediated immunosuppression protects tissues from collateral damage by antipathogen immune…”
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Differential regulation of HIF-1α isoforms in murine macrophages by TLR4 and adenosine A2A receptor agonists
Published in Journal of leukocyte biology (01-09-2009)“…Up‐regulation of adenosine A2A receptors (A2ARs) and the HIF‐1αl. 1 isoform plays an important role in the switch of macrophages from an inflammatory (M1) to…”
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The critical role of adenosine A2A receptors in downregulation of inflammation and immunity in the pathogenesis of infectious diseases
Published in Microbes and infection (01-05-2003)“…Adenosine can be described as a retaliatory metabolite, the production and release of which is usually enhanced under adverse environmental conditions. Binding…”
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T regulatory cells: hypoxia-adenosinergic suppression and re-direction of the immune response
Published in Trends in immunology (01-03-2009)“…T regulatory cells (Treg cells) suppress immune responses to maintain self tolerance, but they also protect cancerous tissues. I propose a model to potentially…”
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Sufficient numbers of anti-tumor T cells is a condition of maximal efficacy of anti-hypoxia-A2-adenosinergic drugs during cancer immunotherapy
Published in Current opinion in pharmacology (01-08-2020)“…•Discoveries of hypoxia-adenosine pathway and credit to teams of contributing authors.•Limitation of anti-hypoxia-adenosinergic treatments in…”
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Hostile, hypoxia-A2-adenosinergic tumor biology as the next barrier to overcome for tumor immunologists
Published in Cancer immunology research (01-07-2014)“…Hypoxia-driven, A2A adenosine receptor (A2AR)-mediated (hypoxia-A2-adenosinergic), T-cell-autonomous immunosuppression was first recognized as critical and…”
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Adenosine A2A Receptor Is Involved in Cell Surface Expression of A2B Receptor
Published in The Journal of biological chemistry (10-12-2010)“…The A2A and A2B adenosine receptors (A2AR and A2BR) are implicated in many physiological processes. However, the mechanisms of their intracellular maturation…”
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Oxygen‐Generating Cryogels Restore T Cell Mediated Cytotoxicity in Hypoxic Tumors
Published in Advanced functional materials (01-09-2021)“…Solid tumors are protected from antitumor immune responses due to their hypoxic microenvironments. Weakening hypoxia‐driven immunosuppression by hyperoxic…”
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Physiological control of immune response and inflammatory tissue damage by hypoxia-inducible factors and adenosine A2A receptors
Published in Annual review of immunology (2004)“…Immune cell-mediated destruction of pathogens may result in excessive collateral damage to normal tissues, and the failure to control activated immune cells…”
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Use of the A 2A adenosine receptor as a physiological immunosuppressor and to engineer inflammation in vivo
Published in Biochemical pharmacology (15-02-2003)“…Inflammation must be inhibited in order to treat, e.g., sepsis or autoimmune diseases or must be selectively enhanced to improve, for example, immunotherapies…”
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