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Targeting CD4+ Cells with Anti-CD4 Conjugated Mertansine-Loaded Nanogels.

Mine CanakciKhushboo SinghOyuntuya MunkhbatSudarvili ShanthalingamAnkita MitraMallory GordonBarbara A OsborneSankaran Thayumanavan
Published in: Biomacromolecules (2020)
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.
Keyphrases
  • cancer therapy
  • drug delivery
  • small molecule
  • nk cells
  • induced apoptosis
  • computed tomography
  • photodynamic therapy
  • papillary thyroid
  • endoplasmic reticulum stress
  • drug release