Cargando…
Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells
Regulatory T cells (Tregs) represent a subpopulation of CD4(+) T cells, which are essential for the maintenance of immunological tolerance. The absence or dysfunction of Tregs can lead to autoimmunity and allergies. The restoration of functional Tregs and/or Treg cell numbers represents a novel and...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724712/ https://www.ncbi.nlm.nih.gov/pubmed/26834751 http://dx.doi.org/10.3389/fimmu.2016.00011 |
_version_ | 1782411571420463104 |
---|---|
author | König, Martin Rharbaoui, Faiza Aigner, Silke Dälken, Benjamin Schüttrumpf, Jörg |
author_facet | König, Martin Rharbaoui, Faiza Aigner, Silke Dälken, Benjamin Schüttrumpf, Jörg |
author_sort | König, Martin |
collection | PubMed |
description | Regulatory T cells (Tregs) represent a subpopulation of CD4(+) T cells, which are essential for the maintenance of immunological tolerance. The absence or dysfunction of Tregs can lead to autoimmunity and allergies. The restoration of functional Tregs and/or Treg cell numbers represents a novel and attractive approach for the treatment of autoimmune diseases, e.g., rheumatoid arthritis (RA). The CD4 cell surface receptor is a target for modulation of T cell function. Monoclonal antibodies (mAbs) against CD4 have previously been tested for the treatment of autoimmune diseases, including RA. Furthermore, in model systems, anti-CD4 antibodies are able to induce tolerance and mediate immunomodulatory effects through a variety of mechanisms. Despite the availability of innovative and effective therapies for RA, many patients still have persistently active disease or experience adverse events that can limit use. A growing body of evidence suggests that Treg modulation could offer a new therapeutic strategy in RA and other autoimmune disorders. Here, we describe tregalizumab (BT-061), which is a novel, non-depleting IgG1 mAb that binds to a unique epitope of CD4. Tregalizumab represents the first humanized anti-CD4 mAb that selectively induces Treg activation. |
format | Online Article Text |
id | pubmed-4724712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47247122016-01-31 Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells König, Martin Rharbaoui, Faiza Aigner, Silke Dälken, Benjamin Schüttrumpf, Jörg Front Immunol Immunology Regulatory T cells (Tregs) represent a subpopulation of CD4(+) T cells, which are essential for the maintenance of immunological tolerance. The absence or dysfunction of Tregs can lead to autoimmunity and allergies. The restoration of functional Tregs and/or Treg cell numbers represents a novel and attractive approach for the treatment of autoimmune diseases, e.g., rheumatoid arthritis (RA). The CD4 cell surface receptor is a target for modulation of T cell function. Monoclonal antibodies (mAbs) against CD4 have previously been tested for the treatment of autoimmune diseases, including RA. Furthermore, in model systems, anti-CD4 antibodies are able to induce tolerance and mediate immunomodulatory effects through a variety of mechanisms. Despite the availability of innovative and effective therapies for RA, many patients still have persistently active disease or experience adverse events that can limit use. A growing body of evidence suggests that Treg modulation could offer a new therapeutic strategy in RA and other autoimmune disorders. Here, we describe tregalizumab (BT-061), which is a novel, non-depleting IgG1 mAb that binds to a unique epitope of CD4. Tregalizumab represents the first humanized anti-CD4 mAb that selectively induces Treg activation. Frontiers Media S.A. 2016-01-25 /pmc/articles/PMC4724712/ /pubmed/26834751 http://dx.doi.org/10.3389/fimmu.2016.00011 Text en Copyright © 2016 König, Rharbaoui, Aigner, Dälken and Schüttrumpf. http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Immunology König, Martin Rharbaoui, Faiza Aigner, Silke Dälken, Benjamin Schüttrumpf, Jörg Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title | Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title_full | Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title_fullStr | Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title_full_unstemmed | Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title_short | Tregalizumab – A Monoclonal Antibody to Target Regulatory T Cells |
title_sort | tregalizumab – a monoclonal antibody to target regulatory t cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724712/ https://www.ncbi.nlm.nih.gov/pubmed/26834751 http://dx.doi.org/10.3389/fimmu.2016.00011 |
work_keys_str_mv | AT konigmartin tregalizumabamonoclonalantibodytotargetregulatorytcells AT rharbaouifaiza tregalizumabamonoclonalantibodytotargetregulatorytcells AT aignersilke tregalizumabamonoclonalantibodytotargetregulatorytcells AT dalkenbenjamin tregalizumabamonoclonalantibodytotargetregulatorytcells AT schuttrumpfjorg tregalizumabamonoclonalantibodytotargetregulatorytcells |