Cargando…
T-Cell Therapy: Options for Infectious Diseases
The emergence of drug-resistant tuberculosis is challenging tuberculosis control worldwide. In the absence of an effective vaccine to prevent primary infection with Mycobacterium tuberculosis and tuberculosis disease, host-directed therapies may offer therapeutic options, particularly for patients w...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583575/ https://www.ncbi.nlm.nih.gov/pubmed/26409284 http://dx.doi.org/10.1093/cid/civ615 |
_version_ | 1782391876125458432 |
---|---|
author | Parida, Shreemanta K. Poiret, Thomas Zhenjiang, Liu Meng, Qingda Heyckendorf, Jan Lange, Christoph Ambati, Aditya S. Rao, Martin V. Valentini, Davide Ferrara, Giovanni Rangelova, Elena Dodoo, Ernest Zumla, Alimuddin Maeurer, Markus |
author_facet | Parida, Shreemanta K. Poiret, Thomas Zhenjiang, Liu Meng, Qingda Heyckendorf, Jan Lange, Christoph Ambati, Aditya S. Rao, Martin V. Valentini, Davide Ferrara, Giovanni Rangelova, Elena Dodoo, Ernest Zumla, Alimuddin Maeurer, Markus |
author_sort | Parida, Shreemanta K. |
collection | PubMed |
description | The emergence of drug-resistant tuberculosis is challenging tuberculosis control worldwide. In the absence of an effective vaccine to prevent primary infection with Mycobacterium tuberculosis and tuberculosis disease, host-directed therapies may offer therapeutic options, particularly for patients with multidrug-resistant and extensively drug-resistant tuberculosis where prognosis is often limited. CD8(+) and CD4(+) T cells mediate antigen-specific adaptive cellular immune responses. Their use in precision immunotherapy in clinical conditions, especially in treating cancer as well as for prevention of life-threatening viral infections in allogeneic transplant recipients, demonstrated safety and clinical efficacy. We review key achievements in T-cell therapy, including the use of recombinant immune recognition molecules (eg, T-cell receptors and CD19 chimeric antigen receptors), and discuss its potential in the clinical management of patients with drug-resistant and refractory tuberculosis failing conventional therapy. |
format | Online Article Text |
id | pubmed-4583575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45835752015-09-28 T-Cell Therapy: Options for Infectious Diseases Parida, Shreemanta K. Poiret, Thomas Zhenjiang, Liu Meng, Qingda Heyckendorf, Jan Lange, Christoph Ambati, Aditya S. Rao, Martin V. Valentini, Davide Ferrara, Giovanni Rangelova, Elena Dodoo, Ernest Zumla, Alimuddin Maeurer, Markus Clin Infect Dis Advances in Tuberculosis Research: A Blueprint for Opportunities The emergence of drug-resistant tuberculosis is challenging tuberculosis control worldwide. In the absence of an effective vaccine to prevent primary infection with Mycobacterium tuberculosis and tuberculosis disease, host-directed therapies may offer therapeutic options, particularly for patients with multidrug-resistant and extensively drug-resistant tuberculosis where prognosis is often limited. CD8(+) and CD4(+) T cells mediate antigen-specific adaptive cellular immune responses. Their use in precision immunotherapy in clinical conditions, especially in treating cancer as well as for prevention of life-threatening viral infections in allogeneic transplant recipients, demonstrated safety and clinical efficacy. We review key achievements in T-cell therapy, including the use of recombinant immune recognition molecules (eg, T-cell receptors and CD19 chimeric antigen receptors), and discuss its potential in the clinical management of patients with drug-resistant and refractory tuberculosis failing conventional therapy. Oxford University Press 2015-10-15 2015-09-16 /pmc/articles/PMC4583575/ /pubmed/26409284 http://dx.doi.org/10.1093/cid/civ615 Text en © The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com. |
spellingShingle | Advances in Tuberculosis Research: A Blueprint for Opportunities Parida, Shreemanta K. Poiret, Thomas Zhenjiang, Liu Meng, Qingda Heyckendorf, Jan Lange, Christoph Ambati, Aditya S. Rao, Martin V. Valentini, Davide Ferrara, Giovanni Rangelova, Elena Dodoo, Ernest Zumla, Alimuddin Maeurer, Markus T-Cell Therapy: Options for Infectious Diseases |
title | T-Cell Therapy: Options for Infectious Diseases |
title_full | T-Cell Therapy: Options for Infectious Diseases |
title_fullStr | T-Cell Therapy: Options for Infectious Diseases |
title_full_unstemmed | T-Cell Therapy: Options for Infectious Diseases |
title_short | T-Cell Therapy: Options for Infectious Diseases |
title_sort | t-cell therapy: options for infectious diseases |
topic | Advances in Tuberculosis Research: A Blueprint for Opportunities |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583575/ https://www.ncbi.nlm.nih.gov/pubmed/26409284 http://dx.doi.org/10.1093/cid/civ615 |
work_keys_str_mv | AT paridashreemantak tcelltherapyoptionsforinfectiousdiseases AT poiretthomas tcelltherapyoptionsforinfectiousdiseases AT zhenjiangliu tcelltherapyoptionsforinfectiousdiseases AT mengqingda tcelltherapyoptionsforinfectiousdiseases AT heyckendorfjan tcelltherapyoptionsforinfectiousdiseases AT langechristoph tcelltherapyoptionsforinfectiousdiseases AT ambatiadityas tcelltherapyoptionsforinfectiousdiseases AT raomartinv tcelltherapyoptionsforinfectiousdiseases AT valentinidavide tcelltherapyoptionsforinfectiousdiseases AT ferraragiovanni tcelltherapyoptionsforinfectiousdiseases AT rangelovaelena tcelltherapyoptionsforinfectiousdiseases AT dodooernest tcelltherapyoptionsforinfectiousdiseases AT zumlaalimuddin tcelltherapyoptionsforinfectiousdiseases AT maeurermarkus tcelltherapyoptionsforinfectiousdiseases |