Ethan M. Shevach

ORCID: 0000-0003-1607-4664
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Monoclonal and Polyclonal Antibodies Research
  • Immune Response and Inflammation
  • CAR-T cell therapy research
  • Glycosylation and Glycoproteins Research
  • Diabetes and associated disorders
  • Cell Adhesion Molecules Research
  • Immunodeficiency and Autoimmune Disorders
  • Cancer Immunotherapy and Biomarkers
  • Cytokine Signaling Pathways and Interactions
  • Atherosclerosis and Cardiovascular Diseases
  • IL-33, ST2, and ILC Pathways
  • RNA Interference and Gene Delivery
  • Galectins and Cancer Biology
  • Toxin Mechanisms and Immunotoxins
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Helicobacter pylori-related gastroenterology studies
  • Systemic Lupus Erythematosus Research
  • Macrophage Migration Inhibitory Factor
  • Immune cells in cancer
  • Transgenic Plants and Applications
  • Cytomegalovirus and herpesvirus research
  • T-cell and Retrovirus Studies

National Institute of Allergy and Infectious Diseases
2016-2025

National Institutes of Health
2016-2025

The Ohio State University
2023

Office of Extramural Research
2009-2015

National Institute of General Medical Sciences
2013

University of Oklahoma Health Sciences Center
2012

Mayo Clinic
2012

New Huadu Business School
2012

National Heart Lung and Blood Institute
1986-2009

Laboratory of Molecular Genetics
1988-2008

Peripheral tolerance may be maintained by a population of regulatory/suppressor T cells that prevent the activation autoreactive recognizing tissue-specific antigens. We have previously shown CD4+CD25+ represent unique suppressor can both initiation organ-specific autoimmune disease after day 3 thymectomy and effector function cloned autoantigen-specific CD4+ cells. To analyze mechanism action these cells, we established an in vitro model system mimics vivo. Purified failed to proliferate...

10.1084/jem.188.2.287 article EN The Journal of Experimental Medicine 1998-07-20

Helios, a member of the Ikaros transcription factor family, is preferentially expressed at mRNA level by regulatory T cells (Treg cells). We evaluated Helios protein expression using newly generated mAb and demonstrated that it in all thymocytes double negative 2 stage thymic development. Although was 100% CD4(+)CD8(-)Foxp3(+) thymocytes, its peripheral lymphoid tissues restricted to subpopulation ( approximately 70%) Foxp3(+) mice humans. Neither mouse nor human naive induced express Foxp3...

10.4049/jimmunol.0904028 article EN The Journal of Immunology 2010-02-25

Abstract CD4+CD25+ T cells represent a unique population of “professional” suppressor that prevent induction organ-specific autoimmune disease. In vitro, were anergic to simulation via the TCR and when cultured with CD4+CD25− cells, markedly suppressed polyclonal cell proliferation by specifically inhibiting production IL-2. Suppression was cytokine independent, contact dependent, required activation suppressors their TCR. Further characterization demonstrated they do not contain memory or...

10.4049/jimmunol.164.1.183 article EN The Journal of Immunology 2000-01-01

Antigen activation of DNA synthesis in immune thymus-derived lymphocytes guinea pigs requires the cooperation macrophages and lymphocytes. We have investigated role histocompatibility determinants this macrophage-lymphocyte interaction using cells from inbred strain 2 13 pigs. The data demonstrate that efficient presentation macrophage-associated antigen to lymphocyte identity between macrophage at some portion major complex. failure allogeneic effectively initiate proliferation was not...

10.1084/jem.138.5.1194 article EN The Journal of Experimental Medicine 1973-11-01

Thymectomy of susceptible strains mice on day 3 life results in a spectrum organ-specific autoimmunity that can be prevented by reconstitution the thymectomized animals early with normal adult lymphocytes. The effectors and suppressors this model have been convincingly shown to CD4+ T cells. It has demonstrated recently regulatory cells prevent disease coexpress CD25. We further characterized population CD4+CD25+ immunoregulatory they suppress not only induction post-thymectomy, but also...

10.4049/jimmunol.160.3.1212 article EN The Journal of Immunology 1998-02-01

We have previously demonstrated that the inhibitory effects of IL-10 on ConA-induced T cell proliferation or IL-2 production by resting murine cells were only observed when macrophages, but not activated B cells, dendritic L used as accessory cells. To further elucidate mechanism action inhibition macrophage costimulatory activity, we a system in which macrophages can develop into effective costimulator and effect this process be studied absence After fixation, no activity for soluble...

10.4049/jimmunol.151.3.1224 article EN The Journal of Immunology 1993-08-01

CD4(+)CD25(+) regulatory T cells inhibit organ-specific autoimmune diseases induced by CD4(+)CD25(-) and are potent suppressors of cell activation in vitro. We demonstrate that also suppress both proliferation IFN-gamma production CD8(+) either polyclonal or Ag-specific stimuli. the responders inhibiting IL-2 up-regulation IL-2Ralpha-chain (CD25) expression. Suppression is mediated via a T-T interaction as activated responses TCR-transgenic stimulated with soluble peptide-MHC class I...

10.4049/jimmunol.167.3.1137 article EN The Journal of Immunology 2001-08-01

Abstract Langerhans cells (LC) constitute a morphologically well-characterized minor subpopulation of the mammalian epidermis whose functional role is still matter conjecture. The hypothesis that LC represent an epidermal equivalent to monocyte-macrophage-histiocyte series supported by recent observations in humans and guinea pigs are only express Fc-IgG receptors, C3 Ia antigens. Using inbred strain 2 13 pigs, we investigated this study whether can mediate same immunologic functions as...

10.4049/jimmunol.121.5.2005 article EN The Journal of Immunology 1978-11-01

CD4(+)CD25(+) regulatory T cells inhibit organ-specific autoimmune diseases induced by CD4(+)CD25(-) and are potent suppressors of cell activation in vitro. Their mechanism suppression remains unknown, but most vitro studies suggest that it is contact-dependent cytokine independent. The role TGF-beta1 suppressor function unclear. While have failed to reverse with anti-transforming growth factor (TGF)-beta1 vitro, one recent study has reported express surface can be completely abrogated high...

10.1084/jem.20020590 article EN The Journal of Experimental Medicine 2002-07-15

A number of recent studies have suggested that the main functional role product immune response (Ir) genes is in process antigen recognition by T lymphocyte. The observation accompanying report interaction macrophage-associated with lymphocytes requires both cells share histocompatibility antigens raised question as to whether macrophage played a genetic control or even if were primary cell which Ir gene expressed. In current study, parental macrophages pulsed an antigen, controlled lacking...

10.1084/jem.138.5.1213 article EN The Journal of Experimental Medicine 1973-11-01

The properties and outcome of an immune response are best predicted by the lymphokine phenotype responding T cells. Cytokines produced CD4+ helper type 1 (Th1) cells mediate delayed hypersensitivity (DTH) inflammatory responses, whereas cytokines Th2 cell functions for antibody production. To determine whether induction Th2-like would modulate response, interleukin 4 (IL-4) was administered to animals with experimental allergic encephalomyelitis (EAE), a prototypic autoimmune disease...

10.1084/jem.180.5.1961 article EN The Journal of Experimental Medicine 1994-11-01

CD4(+)CD25(+) T cells are potent immunoregulatory that suppress TCR-induced proliferation of CD4 and CD8 in vitro by a cell contact-dependent mechanism. Addition IL-2 or anti-CD28 abrogates CD4(+)CD25(+)-mediated suppression has been assumed to "break suppression." We examined mRNA quantitative PCR cocultures mouse CD4(+)CD25(-) cells. Although gene transcription was inhibited the presence absence exogenous IL-2, addition stimulated endogenous production. Surprisingly, also restored...

10.4049/jimmunol.172.11.6519 article EN The Journal of Immunology 2004-06-01
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