| Literature DB >> 32383874 |
Mine Canakci1,2,3, Khushboo Singh1,4, Oyuntuya Munkhbat1, Sudarvili Shanthalingam2, Ankita Mitra2, Mallory Gordon1, Barbara A Osborne2,3,4, S Thayumanavan1,3,4.
Abstract
CD4+ T lymphocytes play an important role in controlling many malignancies. The modulation of CD4+ T cells through immunomodulatory or cytotoxic drugs could change the course of disease progression for disorders such as autoimmunity, immunodeficiency, and cancer. Here, we demonstrate that anti-CD4 conjugated polymeric nanogels can deliver a small molecule cargo to primary CD4+ T cells and a CD4high T cell lymphoma. The antibody conjugation not only increased the uptake efficiency of the nanogel (NG) by CD4+ T cells but also decreased the non-specific uptake of the NG by CD4- lymphocytes. For T lymphoma cell lines, the mertansine-loaded conjugate displayed a dose-dependent cell growth inhibition at 17 ng/mL antibody concentration. On the other hand, antibody-drug conjugate (ADC)-type formulation of the anti-CD4 reached similar levels of cell growth inhibition only at the significantly higher concentration of 1.8 μg/mL. NG and antibody conjugates have the advantage of carrying a large payload to a defined target in a more efficient manner as it needs far less antibody to achieve a similar outcome.Entities:
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Year: 2020 PMID: 32383874 PMCID: PMC7354862 DOI: 10.1021/acs.biomac.0c00442
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988