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CD30: from basic research to cancer therapy.
- Source :
-
Immunologic research [Immunol Res] 2013 Dec; Vol. 57 (1-3), pp. 151-8. - Publication Year :
- 2013
-
Abstract
- The FDA recently approved an agonistic anti-CD30 drug conjugate, Brentuximab vedotin, for the treatment for CD30-positive lymphomas. The potent clinical activity of Brentuximab vedotin in Hodgkin's lymphoma and anaplastic large-cell lymphoma was greeted with great enthusiasm by oncologists as it provided a new treatment modality for these diseases. In this review, we will describe how we obtained the hybridoma by pursuing a basic research experiment unrelated to CD30. I will also review what we know about the normal biological functions of CD30 that were studied primarily in murine models of disease but also in patients. The picture emerging is that one of the primary functions of CD30 is the control of memory cells providing costimulation and trafficking information or inducing apoptosis in a microenvironment and cytokine milieu-dependent manner.
- Subjects :
- Animals
Antibodies, Monoclonal pharmacology
Antibodies, Monoclonal therapeutic use
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Brentuximab Vedotin
CD30 Ligand genetics
CD30 Ligand metabolism
CD4-Positive T-Lymphocytes immunology
CD4-Positive T-Lymphocytes metabolism
CD8-Positive T-Lymphocytes immunology
CD8-Positive T-Lymphocytes metabolism
Colitis genetics
Colitis immunology
Colitis metabolism
Cytotoxicity, Immunologic
Disease Models, Animal
Drug Screening Assays, Antitumor
Gene Expression Regulation, Neoplastic
Graft vs Host Disease immunology
Graft vs Host Disease metabolism
HLA Antigens immunology
Humans
Immunoconjugates pharmacology
Immunoconjugates therapeutic use
Immunologic Memory
Ki-1 Antigen genetics
Ki-1 Antigen immunology
Ki-1 Antigen metabolism
Mice
Mice, Knockout
Neoplasms drug therapy
Neoplasms genetics
Neoplasms immunology
Neoplasms metabolism
Research
Signal Transduction
Ki-1 Antigen antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1559-0755
- Volume :
- 57
- Issue :
- 1-3
- Database :
- MEDLINE
- Journal :
- Immunologic research
- Publication Type :
- Academic Journal
- Accession number :
- 24233555
- Full Text :
- https://doi.org/10.1007/s12026-013-8464-1