scholarly journals The r144 Major Histocompatibility Complex Class I-Like Gene of Rat Cytomegalovirus Is Dispensable for both Acute and Long-Term Infection in the Immunocompromised Host

2000 ◽  
Vol 74 (2) ◽  
pp. 1045-1050 ◽  
Author(s):  
Patrick S. Beisser ◽  
Jeroen S. Kloover ◽  
Gert E. L. M. Grauls ◽  
Marinus J. Blok ◽  
Cathrien A. Bruggeman ◽  
...  

ABSTRACT The rat cytomegalovirus (RCMV) r144 gene encodes a polypeptide homologous to major histocompatibility complex class I heavy chains. To study the role of r144 in virus replication, an RCMV r144 null mutant strain (RCMVΔr144) was generated. This strain replicated with efficiency similar to that of wild-type (WT) RCMV in vitro. Additionally, WT RCMV and RCMVΔr144 were found not to differ in their replication characteristics in vivo. First, the survival rate was similar among groups of immunosuppressed rats infected with either RCMVΔr144 or WT RCMV. Second, the dissemination of virus did not differ in either RCMVΔr144- or WT RCMV-infected, immunosuppressed rats, either in the acute phase of infection or approximately 1 year after infection. These data indicate that the RCMV r144 gene is essential neither for virus replication in the acute phase of infection nor for long-term infection in immunocompromised rats. Interestingly, in a local infection model in which footpads of immunosuppressed rats were inoculated with virus, a significantly higher number of infiltrating macrophage cells as well as of CD8+ T cells was observed in WT RCMV-infected paws than in RCMVΔr144-infected paws. This suggests that r144 might function in the interaction with these leukocytes in vivo.

2007 ◽  
Vol 14 (5) ◽  
pp. 538-543 ◽  
Author(s):  
Pablo D. Becker ◽  
Miriam Nörder ◽  
Carlos A. Guzmán ◽  
Saul Grinstein

ABSTRACT Adamantylamide l-alanyl-d-isoglutamine (AdDP) is a synthetic adjuvant which belongs to the family of the desmuramyl peptides. AdDP exerts its adjuvant properties when it is administered either by the parenteral or by the mucosal route, leading to the elicitation of strong humoral responses at both the systemic and the mucosal levels. However, very little is known about the effect of AdDP on cellular immunity. Here we demonstrate that AdDP is able to stimulate cellular responses, which are characterized by the release of gamma interferon by CD8+ T cells when they are restimulated with a major histocompatibility complex class I-restricted peptide and strong in vivo lymphocyte-mediated cytotoxic activity. The capacity of AdDP to stimulate the elicitation of both cellular and humoral adaptive responses makes this adjuvant a promising tool for the development of mucosal vaccine formulations.


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