In: PLOS ONE
	 5(7), e6317
	
      
        
          
             [PDF, 608kB]
          
        
      
Abstract
Control of gammaherpesvirus infections requires a complex, well orchestrated immune response regulated by positive and negative co-signaling molecules. While the impact of co-stimulatory molecules has been addressed in various studies, the role of co-inhibitory receptors has not been tested. The ITIM-bearing CEACAM1 is an inhibitory receptor expressed by a variety of immune cells, including B, T and NK cells. Using Ceacam1(-/-) mice, we analyzed the in vivo function of CEACAM1 during acute and latent murine gammaherpesvirus 68 (MHV-68) infection. During acute lytic replication, we observed lower virus titers in the lungs of Ceacam1(-/-) mice than in WT mice. In contrast, during latency amplification, Ceacam1(-/-) mice displayed increased splenomegaly and a higher latent viral load in the spleen. Analysis of the immune response revealed increased virus-specific antibody levels in Ceacam1(-/-) mice, while the magnitude of the T cell-mediated antiviral immune response was reduced. These findings suggest that inhibitory receptors can modulate the efficacy of immune responses against gammaherpesvirus infections.
| Dokumententyp: | Zeitschriftenartikel | 
|---|---|
| Publikationsform: | Publisher's Version | 
| Fakultät: | Medizin | 
| Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit | 
| URN: | urn:nbn:de:bvb:19-epub-15343-5 | 
| ISSN: | 1932-6203 | 
| Sprache: | Englisch | 
| Dokumenten ID: | 15343 | 
| Datum der Veröffentlichung auf Open Access LMU: | 27. Mai 2013 08:56 | 
| Letzte Änderungen: | 04. Nov. 2020 12:56 | 
 
		 
	 
    



