Antibody technologies

Projects

Characterization of HERV envelope proteins with the aim of developing therapeutic antibodies for HERV-associated autoimmune and tumor diseases

fluoreszenzmikro­skopische Aufnahme transfizierter HEK293F-Zellen mit HERV-Fc1 Env-­spezifischen Antikörper 3D3
© Fraunhofer IZI
Fluorescence microscopy images of transfected HEK293F cells with the HERV-Fc1 Env-specific antibody 3D3 (red) show the occurrence of the envelope protein inside the cell in the case of permeabilized cells (above) and on the cell surface in the case of cells with an intact cell membrane.

Human endogenous retroviruses (HERVs) and, more specifically, their envelope proteins are suspected of transporting diseases such as multiple sclerosis, rheumatism and tumor diseases. The actual function of these specific factors is yet to be clarified. Cellular damage and the misdirected stimulation of the immune system caused by HERVs are presumed to be disease mechanisms. New findings should help shed light on the role played by HERVs in the emergence of autoimmune and tumor diseases.

As part of a joint research project with Halle University Hospital, researchers at Fraunhofer IZI were able to manufacture HERV envelope proteins using biotechnological methods and characterize their biological activity. These proteins also served as antigens for generating both polyclonal and monoclonal antibodies. Furthermore, the biological effects of HERV envelope proteins were able to be examined in cell cultures and experimental animals, and their immune-­stimulatory properties characterized. Together with the project partners from Halle University Hospital, HERV sequences could also be identified in various tumor entities. 

The research project is thus paving the way for new therapeutic procedures in the treatment of autoimmune and tumor diseases.

The project “Characterization of HERV envelope proteins aimed at developing therapeutic antibodies for HERV-­associated autoimmune and tumor diseases” was funded by the European Regional Development Fund (ERDF) and the State of Saxony-Anhalt. The funding was awarded as part of the “Saxony-Anhalt SCIENCE – FOCUS” program, through which the State of Saxony-Anhalt supports specialist research activities and innovative research projects in the field of science.

Publications

Other projects

  • DFG: “Identifizierung von Abeta-Peptid-Mustern im Gehirn von Alzheimer-Patienten mit neuen monoklonalen Antikörpern” (“Identification of Abeta peptide patterns in the brain of Alzheimer’s patients with monoclonal antibodies”) (2226/17-1ï SCHI 1437/4-1)
    Applicant: Prof. Dr Steffen Roßner, Leipzig, and Dr Stephan Schilling, Halle/S.
  • DFG: “Enzymatische Regulation der Bioaktivität von CCL2 bei neuroinflammatorischen Prozessen” (“Enzymatic Bioactivity Regulation of CCL2 in Neuroinflammatory Processes”) (RO 2226/15-1ï SCHI 1437/2-1)
    Applicant: Prof. Dr Steffen Roßner, Leipzig, and Dr Stephan Schilling, Halle/S.