Targeting CD38 in Neoplasms and Non-Cancer Diseases

被引:20
作者
Szlasa, Wojciech [1 ]
Czarny, Jakub [2 ]
Sauer, Natalia [3 ]
Rakoczy, Katarzyna [1 ]
Szymanska, Natalia [1 ]
Stecko, Jakub [1 ]
Kolodziej, Maksymilian [2 ]
Kazmierczak, Maciej [4 ]
Barg, Ewa [5 ]
机构
[1] Wroclaw Med Univ, Fac Med, PL-50367 Wroclaw, Poland
[2] Poznan Univ Med Sci, Fac Med, PL-61701 Poznan, Poland
[3] Wroclaw Med Univ, Fac Pharm, PL-50367 Wroclaw, Poland
[4] Poznan Univ Med Sci, Dept Hematol & Bone Marrow Transplantat, PL-61701 Poznan, Poland
[5] Wroclaw Med Univ, Fac Pharm, Dept Basic Med Sci, PL-50556 Wroclaw, Poland
关键词
CD38; multiple myeloma; anticancer therapy; cancer; CHRONIC LYMPHOCYTIC-LEUKEMIA; HEMATOPOIETIC STEM-CELLS; HIV-INFECTED PATIENTS; CD8(+) T-LYMPHOCYTES; ADP-RIBOSYL CYCLASE; MULTIPLE-MYELOMA; OPEN-LABEL; ANTIBODY DARATUMUMAB; ANTITUMOR-ACTIVITY; B-CELLS;
D O I
10.3390/cancers14174169
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. 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.
引用
收藏
页数:28
相关论文
共 203 条
[1]   Neutralizing Antibody Responses Against Sars-Cov-2 in Patients with Plasma Cell Disorders Who Are on Active Treatment after Two Doses of mRNA Vaccination [J].
Abdallah, Al-Ola ;
Mahmoudjafari, Zahra ;
Mohan, Meera ;
McGuirk, Joseph P. ;
Remker, Cassie ;
Foss, Margaret ;
Karloff, Ellie ;
Fitch, Heather ;
Mohyuddin, Ghulam Rehman ;
Atrash, Shebli .
BLOOD, 2021, 138 :3804-+
[2]   Daratumumab for Antibody-mediated Rejection in Heart Transplant-A Novel Therapy: Successful Treatment of Antibody-mediated Rejection [J].
Aguilera Agudo, Cristina ;
Gomez Bueno, Manuel ;
Krsnik Castello, Isabel .
TRANSPLANTATION, 2021, 105 (03) :E30-E31
[3]   Multiple Myeloma in the Time of COVID-19 [J].
Al Saleh, Abdullah S. ;
Sher, Taimur ;
Gertz, Morie A. .
ACTA HAEMATOLOGICA, 2020, 143 (05) :410-416
[4]   CD38 Is Robustly Induced in Human Macrophages and Monocytes in Inflammatory Conditions [J].
Amici, Stephanie A. ;
Young, Nicholas A. ;
Narvaez-Miranda, Janiret ;
Jablonski, Kyle A. ;
Arcos, Jesus ;
Rosas, Lucia ;
Papenfuss, Tracey L. ;
Torrelles, Jordi B. ;
Jarjour, Wael N. ;
Guerau-de-Arellano, Mireia .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[5]  
[Anonymous], 2015, CANC CELL MICROENVIR
[6]   The aggressive peripheral T-cell lymphomas: 2017 [J].
Armitage, James O. .
AMERICAN JOURNAL OF HEMATOLOGY, 2017, 92 (07) :706-715
[7]   Isatuximab plus pomalidomide and low-dose dexamethasone versus pomalidomide and low-dose dexamethasone in patients with relapsed and refractory multiple myeloma (ICARIA-MM): a randomised, multicentre, open-label, phase 3 study [J].
Attal, Michel ;
Richardson, Paul G. ;
Rajkumar, S. Vincent ;
San-Miguel, Jesus ;
Beksac, Meral ;
Spicka, Ivan ;
Leleu, Xavier ;
Schjesvold, Fredrik ;
Moreau, Philippe ;
Dimopoulos, Meletios A. ;
Huang, Jeffrey Shang-Yi ;
Minarik, Jiri ;
Cavo, Michele ;
Prince, H. Miles ;
Mace, Sandrine ;
Corzo, Kathryn P. ;
Campana, Frank ;
Le-Guennec, Solenn ;
Dubin, Franck ;
Anderson, Kenneth C. .
LANCET, 2019, 394 (10214) :2096-2107
[8]   Phase I Study of Venetoclax Plus Daratumumab and Dexamethasone, With or Without Bortezomib, in Patients With Relapsed or Refractory Multiple Myeloma With and Without t(11;14) [J].
Bahlis, Nizar J. ;
Baz, Rachid ;
Harrison, Simon J. ;
Quach, Hang ;
Ho, Shir-Jing ;
Vangsted, Annette Juul ;
Plesner, Torben ;
Moreau, Philippe ;
Gibbs, Simon D. ;
Coppola, Sheryl ;
Yang, Xiaoqing ;
Al Masud, Abdullah ;
Ross, Jeremy A. ;
Bueno, Orlando ;
Kaufman, Jonathan L. .
JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (32) :3602-+
[9]   Upregulation of CD38 gene expression in leukemic B cells by interferon types I and II [J].
Bauvois, B ;
Durant, L ;
Laboureau, J ;
Barthélémy, E ;
Rouillard, D ;
Boulla, G ;
Deterre, P .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1999, 19 (09) :1059-1066
[10]   Cellular expression of CD markers in immune thrombocytopenic purpura: implications for prognosis [J].
Behzad, Masumeh Maleki ;
Asnafi, Ali Amin ;
Jalalifar, Mohammad Ali ;
Moghtadaei, Mostafa ;
Jaseb, Kaveh ;
Saki, Najmaldin .
APMIS, 2018, 126 (06) :523-532