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Projekt Druckansicht

Der Einfluss von CEACAM1 bei der anti-viralen Immunantwort

Fachliche Zuordnung Immunologie
Virologie
Förderung Förderung von 2016 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 287900951
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

The object of the project was to determine the role of CEACAM1 during virus infection. To do so we use CEACAM1 deficient mice, CEACAM1 transgenic mice, and CEACAM1 activating antibodies during infection with the lymphocytic choriomeningitis virus (LCMV) and vesicular stomatitis virus (VSV). In addition, we analyzed the role of CEACAM1 on human virus-specific CD8+ T cells in in vitro experiments. Identifying the most important mechanisms, how CEACAM1 influences immune cells was another goal. We found that CEACAM1 was important for maintaining the splenic architecture. Lack of CEACAM1 reduced the amount of CD169+ macrophages, limited enforced viral replication and resulted in reduced innate immune activation after infection with VSV. Furthermore, we found that B cell intrinsic expression of CEACAM1 was essential for survival of proliferating B cells. Therefore, lack of CEACAM1 in B cells limited antiviral B cell responses during VSV infection. During infection with LCMV, CEACAM1 was upregulated in CD8+ T cells. Lack of CEACAM1 on CD8+ T cells limited T cell expansion and resulted in virus persistence and higher immunopathology. Notably, activation of CEACAM1 by an anti-CEACAM1 antibody could restore CD8+ T cell function, led to fast virus clearance and lower immunopathology. Treatment of human virus-specific CD8+ T cells similarly enhanced CD8+ T cell function, which might make CEACAM1 a useful tool to modulate CD8+ T cell responses. Further evaluation has to be done to validate the role of CEACAM1 in human immune response and elucidate potential therapeutic applications.

Projektbezogene Publikationen (Auswahl)

 
 

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