Microgels as Platforms for Antibody‐Mediated Cytokine Scavenging

Author:

Boesveld Sarah1,Kittel Yonca234,Luo Yizhao1,Jans Alexander1,Oezcifci Burak25,Bartneck Matthias1,Preisinger Christian6,Rommel Dirk23,Haraszti Tamás23,Centeno Silvia P.2,Boersma Arnold J.25,De Laporte Laura237ORCID,Trautwein Christian1,Kuehne Alexander J. C.4ORCID,Strnad Pavel1ORCID

Affiliation:

1. Department of Internal Medicine III University Hospital RWTH Aachen University Pauwelsstraße 30 52074 Aachen Germany

2. DWI‐Leibniz Institute for Interactive Materials RWTH Aachen University Forckenbeckstraße 50 52074 Aachen Germany

3. Institute for Technical and Macromolecular Chemistry (ITMC) RWTH Aachen University Worringerweg 2 52074 Aachen Germany

4. Institute of Organic and Macromolecular Chemistry Ulm University Albert‐Einstein‐Allee 11 89081 Ulm Germany

5. Department of Cellular Protein Chemistry Bijvoet Center for Biomolecular Research Utrecht University Padualaan 8 Utrecht 3584 CH The Netherlands

6. Proteomics Facility Interdisciplinary Centre for Clinical Research (IZKF) Medical School RWTH Aachen University Pauwelsstraße 30 52074 Aachen Germany

7. Advanced Materials for Biomedicine (AMB), Institute of Applied Medical Engineering (AME) Department of Center for Biohybrid Medical Systems (CBMS) Forckenbeckstraße 55 52074 Aachen Germany

Abstract

AbstractTherapeutic antibodies are the key treatment option for various cytokine‐mediated diseases, such as rheumatoid arthritis, psoriasis, and inflammatory bowel disease. However, systemic injection of these antibodies can cause side effects and suppress the immune system. Moreover, clearance of therapeutic antibodies from the blood is limiting their efficacy. Here, water‐swollen microgels are produced with a size of 25 µm using droplet‐based microfluidics. The microgels are functionalized with TNFα antibodies to locally scavenge the pro‐inflammatory cytokine TNFα. Homogeneous distribution of TNFα‐antibodies is shown throughout the microgel network and demonstrates specific antibody‐antigen binding using confocal microscopy and FLIM‐FRET measurements. Due to the large internal accessibility of the microgel network, its capacity to bind TNFα is extremely high. At a TNFα concentration of 2.5 µg mL−1, the microgels are able to scavenge 88% of the cytokine. Cell culture experiments reveal the therapeutic potential of these microgels by protecting HT29 colorectal adenocarcinoma cells from TNFα toxicity and resulting in a significant reduction of COX II and IL8 production of the cells. When the microgels are incubated with stimulated human macrophages, to mimic the in vivo situation of inflammatory bowel disease, the microgels scavenge almost all TNFα that is produced by the cells.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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