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Targeting CD38 in Neoplasms and Non-Cancer Diseases

SIMPLE SUMMARY: CD38 remains an interesting target for anticancer therapy. Its relatively high abundance in neoplasms and crucial impact on NAD+/cADPR metabolism and the activity of T cells allows for changing the immune response in autoimmune diseases, neoplasms, and finally the induction of cell d...

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Autores principales: Szlasa, Wojciech, Czarny, Jakub, Sauer, Natalia, Rakoczy, Katarzyna, Szymańska, Natalia, Stecko, Jakub, Kołodziej, Maksymilian, Kaźmierczak, Maciej, Barg, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454480/
https://www.ncbi.nlm.nih.gov/pubmed/36077708
http://dx.doi.org/10.3390/cancers14174169
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author Szlasa, Wojciech
Czarny, Jakub
Sauer, Natalia
Rakoczy, Katarzyna
Szymańska, Natalia
Stecko, Jakub
Kołodziej, Maksymilian
Kaźmierczak, Maciej
Barg, Ewa
author_facet Szlasa, Wojciech
Czarny, Jakub
Sauer, Natalia
Rakoczy, Katarzyna
Szymańska, Natalia
Stecko, Jakub
Kołodziej, Maksymilian
Kaźmierczak, Maciej
Barg, Ewa
author_sort Szlasa, Wojciech
collection PubMed
description SIMPLE SUMMARY: CD38 remains an interesting target for anticancer therapy. Its relatively high abundance in neoplasms and crucial impact on NAD+/cADPR metabolism and the activity of T cells allows for changing the immune response in autoimmune diseases, neoplasms, and finally the induction of cell death. Antibody-dependent cell cytotoxicity is responsible for cell death induced by targeting the tumor with anti-CD38 antibodies, such as daratumumab. A wide range of laboratory experiments and clinical trials show an especially promising role of anti-CD38 therapy against multiple myeloma, NK cell lymphomas, and CD19- B-cell malignancies. More studies are required to include more diseases in the therapeutic protocols involving the modulation of CD38 activity. ABSTRACT: CD38 is a myeloid antigen present both on the cell membrane and in the intracellular compartment of the cell. Its occurrence is often enhanced in cancer cells, thus making it a potential target in anticancer therapy. Daratumumab and isatuximab already received FDA approval, and novel agents such as MOR202, TAK079 and TNB-738 undergo clinical trials. Also, novel therapeutics such as SAR442085 aim to outrank the older antibodies against CD38. Multiple myeloma and immunoglobulin light-chain amyloidosis may be effectively treated with anti-CD38 immunotherapy. Its role in other hematological malignancies is also important concerning both diagnostic process and potential treatment in the future. Aside from the hematological malignancies, CD38 remains a potential target in gastrointestinal, neurological and pulmonary system disorders. Due to the strong interaction of CD38 with TCR and CD16 on T cells, it may also serve as the biomarker in transplant rejection in renal transplant patients. Besides, CD38 finds its role outside oncology in systemic lupus erythematosus and collagen-induced arthritis. CD38 plays an important role in viral infections, including AIDS and COVID-19. Most of the undergoing clinical trials focus on the use of anti-CD38 antibodies in the therapy of multiple myeloma, CD19- B-cell malignancies, and NK cell lymphomas. This review focuses on targeting CD38 in cancer and non-cancerous diseases using antibodies, cell-based therapies and CD38 inhibitors. We also provide a summary of current clinical trials targeting CD38.
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spelling pubmed-94544802022-09-09 Targeting CD38 in Neoplasms and Non-Cancer Diseases Szlasa, Wojciech Czarny, Jakub Sauer, Natalia Rakoczy, Katarzyna Szymańska, Natalia Stecko, Jakub Kołodziej, Maksymilian Kaźmierczak, Maciej Barg, Ewa Cancers (Basel) Review SIMPLE SUMMARY: CD38 remains an interesting target for anticancer therapy. Its relatively high abundance in neoplasms and crucial impact on NAD+/cADPR metabolism and the activity of T cells allows for changing the immune response in autoimmune diseases, neoplasms, and finally the induction of cell death. Antibody-dependent cell cytotoxicity is responsible for cell death induced by targeting the tumor with anti-CD38 antibodies, such as daratumumab. A wide range of laboratory experiments and clinical trials show an especially promising role of anti-CD38 therapy against multiple myeloma, NK cell lymphomas, and CD19- B-cell malignancies. More studies are required to include more diseases in the therapeutic protocols involving the modulation of CD38 activity. ABSTRACT: CD38 is a myeloid antigen present both on the cell membrane and in the intracellular compartment of the cell. Its occurrence is often enhanced in cancer cells, thus making it a potential target in anticancer therapy. Daratumumab and isatuximab already received FDA approval, and novel agents such as MOR202, TAK079 and TNB-738 undergo clinical trials. Also, novel therapeutics such as SAR442085 aim to outrank the older antibodies against CD38. Multiple myeloma and immunoglobulin light-chain amyloidosis may be effectively treated with anti-CD38 immunotherapy. Its role in other hematological malignancies is also important concerning both diagnostic process and potential treatment in the future. Aside from the hematological malignancies, CD38 remains a potential target in gastrointestinal, neurological and pulmonary system disorders. Due to the strong interaction of CD38 with TCR and CD16 on T cells, it may also serve as the biomarker in transplant rejection in renal transplant patients. Besides, CD38 finds its role outside oncology in systemic lupus erythematosus and collagen-induced arthritis. CD38 plays an important role in viral infections, including AIDS and COVID-19. Most of the undergoing clinical trials focus on the use of anti-CD38 antibodies in the therapy of multiple myeloma, CD19- B-cell malignancies, and NK cell lymphomas. This review focuses on targeting CD38 in cancer and non-cancerous diseases using antibodies, cell-based therapies and CD38 inhibitors. We also provide a summary of current clinical trials targeting CD38. MDPI 2022-08-28 /pmc/articles/PMC9454480/ /pubmed/36077708 http://dx.doi.org/10.3390/cancers14174169 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Szlasa, Wojciech
Czarny, Jakub
Sauer, Natalia
Rakoczy, Katarzyna
Szymańska, Natalia
Stecko, Jakub
Kołodziej, Maksymilian
Kaźmierczak, Maciej
Barg, Ewa
Targeting CD38 in Neoplasms and Non-Cancer Diseases
title Targeting CD38 in Neoplasms and Non-Cancer Diseases
title_full Targeting CD38 in Neoplasms and Non-Cancer Diseases
title_fullStr Targeting CD38 in Neoplasms and Non-Cancer Diseases
title_full_unstemmed Targeting CD38 in Neoplasms and Non-Cancer Diseases
title_short Targeting CD38 in Neoplasms and Non-Cancer Diseases
title_sort targeting cd38 in neoplasms and non-cancer diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454480/
https://www.ncbi.nlm.nih.gov/pubmed/36077708
http://dx.doi.org/10.3390/cancers14174169
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