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Surfactant-Free Poly(styrene-<i>co</i>-glycidyl methacrylate) Particles with Surface-Bound Antibodies for Activation and Proliferation of Human T Cells
11
Citations
37
References
2010
Year
Surfactant-free PolyPolymer ParticlesEngineeringImmunologyImmunologic MechanismAntigen ProcessingBiomedical EngineeringImmune SystemImmunotherapyPeg Chain LengthProtein NanoparticlesSurface-bound AntibodiesImmunochemistryAntibody EngineeringPolymer ChemistryHuman T CellsImmunoengineeringT Cell ImmunityCell BiologyPolymer ColloidsPolymer-drug ConjugateCellular Immune ResponseMedicine
In this article, we present our results on the design of new polymeric carriers for antibodies. Polymer colloids based on poly(styrene-co-glycidyl methacrylate) were synthesized by surfactant-free emulsion polymerization. Obtained polymer particles stabilized by grafted poly(ethylene glycol) (PEG) chains and carrying active epoxy groups were used for the covalent immobilization of activating antibodies against the human surface proteins CD (cluster of differentiation) 3 and CD28. The particle-antibody conjugates were employed for the stimulation of human CD4 memory T cells. This was analyzed by the up-regulation of the activation markers CD69 and CD25 on T cells and T cell proliferation as assessed by the dilution of a fluorescent dye on dividing daughter T cells. The particle-antibody conjugates were able to stimulate T cells at least as efficiently as conventional methods, e.g., surface-immobilized antibodies. Furthermore, an increase of the PEG chain length of the particles decreased the efficiency of the particle-antibody conjugates to activate T cells.
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