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Targeting CD22 for the Treatment of B-Cell Malignancies

Immunotherapeutic agents play an increasingly important role in the treatment of B-cell malignancies. CD19 and CD20 are common targets for lymphoid malignancies, though patients who relapse have few therapeutic options remaining. CD22 is a cell surface sialoglycoprotein uniquely present on B-cells a...

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Autores principales: Shah, Nikesh N, Sokol, Lubomir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275043/
https://www.ncbi.nlm.nih.gov/pubmed/34262884
http://dx.doi.org/10.2147/ITT.S288546
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author Shah, Nikesh N
Sokol, Lubomir
author_facet Shah, Nikesh N
Sokol, Lubomir
author_sort Shah, Nikesh N
collection PubMed
description Immunotherapeutic agents play an increasingly important role in the treatment of B-cell malignancies. CD19 and CD20 are common targets for lymphoid malignancies, though patients who relapse have few therapeutic options remaining. CD22 is a cell surface sialoglycoprotein uniquely present on B-cells and regulates B-cell function and proliferation. Thus, it is an appealing therapeutic target for autoimmune disorders and B-cell malignancies. A variety of therapies targeting CD22 have been developed, including monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, chimeric antigen receptor T cells, and bispecific antibodies. Here, we review the biology of CD22 and key therapies targeting CD22 in lymphoid malignancies.
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spelling pubmed-82750432021-07-13 Targeting CD22 for the Treatment of B-Cell Malignancies Shah, Nikesh N Sokol, Lubomir Immunotargets Ther Review Immunotherapeutic agents play an increasingly important role in the treatment of B-cell malignancies. CD19 and CD20 are common targets for lymphoid malignancies, though patients who relapse have few therapeutic options remaining. CD22 is a cell surface sialoglycoprotein uniquely present on B-cells and regulates B-cell function and proliferation. Thus, it is an appealing therapeutic target for autoimmune disorders and B-cell malignancies. A variety of therapies targeting CD22 have been developed, including monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, chimeric antigen receptor T cells, and bispecific antibodies. Here, we review the biology of CD22 and key therapies targeting CD22 in lymphoid malignancies. Dove 2021-07-06 /pmc/articles/PMC8275043/ /pubmed/34262884 http://dx.doi.org/10.2147/ITT.S288546 Text en © 2021 Shah and Sokol. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Shah, Nikesh N
Sokol, Lubomir
Targeting CD22 for the Treatment of B-Cell Malignancies
title Targeting CD22 for the Treatment of B-Cell Malignancies
title_full Targeting CD22 for the Treatment of B-Cell Malignancies
title_fullStr Targeting CD22 for the Treatment of B-Cell Malignancies
title_full_unstemmed Targeting CD22 for the Treatment of B-Cell Malignancies
title_short Targeting CD22 for the Treatment of B-Cell Malignancies
title_sort targeting cd22 for the treatment of b-cell malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275043/
https://www.ncbi.nlm.nih.gov/pubmed/34262884
http://dx.doi.org/10.2147/ITT.S288546
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