Promising Immunotherapeutic Modalities for B-Cell Lymphoproliferative Disorders
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
FV40145
This work was supported by the the project no. FV40145 Genetically modified donor T cells as a universal cell source for the immunotherapy of tumors using T lymphocytes equipped with a chimeric antigen receptor (CAR)
PubMed
34768899
PubMed Central
PMC8584080
DOI
10.3390/ijms222111470
PII: ijms222111470
Knihovny.cz E-zdroje
- Klíčová slova
- antibody-drug conjugates, bispecific antibodies, brentuximab vedotin, epcoritamab, glofitamab, immunotherapy, mosenutuzumab, polatuzumab vedotin,
- MeSH
- B-buněčný lymfom farmakoterapie imunologie patologie MeSH
- imunokonjugáty terapeutické užití MeSH
- imunoterapie metody MeSH
- lidé MeSH
- lymfoproliferativní nemoci farmakoterapie imunologie patologie MeSH
- monoklonální protilátky terapeutické užití MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- imunokonjugáty MeSH
- monoklonální protilátky MeSH
Over the last few years, treatment principles have been changed towards more targeted therapy for many B-cell lymphoma subtypes and in chronic lymphocytic leukemia (CLL). Immunotherapeutic modalities, namely monoclonal antibodies (mAbs), bispecific antibodies (bsAbs), antibody-drug conjugates (ADCs), and chimeric antigen receptor T (CAR-T) cell therapy, commonly use B-cell-associated antigens (CD19, CD20, CD22, and CD79b) as one of their targets. T-cell engagers (TCEs), a subclass of bsAbs, work on a similar mechanism as CAR-T cell therapy without the need of previous T-cell manipulation. Currently, several anti-CD20xCD3 TCEs have demonstrated promising efficacy across different lymphoma subtypes with slightly better outcomes in the indolent subset. Anti-CD19xCD3 TCEs are being developed as well but only blinatumomab has been evaluated in clinical trials yet. The results are not so impressive as those with anti-CD19 CAR-T cell therapy. Antibody-drug conjugates targeting different B-cell antigens (CD30, CD79b, CD19) seem to be effective in combination with mAbs, standard chemoimmunotherapy, or immune checkpoint inhibitors. Further investigation will show whether immunotherapy alone or in combinatory regimens has potential to replace chemotherapeutic agents from the first line treatment.
Department of Haematooncology University Hospital Ostrava 708 52 Ostrava Czech Republic
Faculty of Medicine University of Ostrava 708 52 Ostrava Czech Republic
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