Pre-existing immunity to pathogenic Listeria monocytogenes does not prevent induction of immune responses to feline immunodeficiency virus by a novel recombinant Listeria monocytogenes vaccine

Vaccine ◽  
2005 ◽  
Vol 23 (12) ◽  
pp. 1479-1490 ◽  
Author(s):  
Rosemary Stevens ◽  
Alora LaVoy ◽  
Shila Nordone ◽  
MaryJo Burkhard ◽  
Gregg A. Dean
Viruses ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 984
Author(s):  
Simões ◽  
LaVoy ◽  
Dean

Regulatory T cells (Treg) are key players in the maintenance of peripheral tolerance, preventing autoimmune diseases and restraining chronic inflammatory diseases. Evidence suggests Treg cells and NK cells have important roles in feline immunodeficiency virus (FIV) pathogenesis; however, in vivo studies investigating the interplay between these two cell populations are lacking. We previously described innate immune defects in FIV-infected cats characterized by cytokine deficits and impaired natural killer cell (NK) and NK T cell (NKT) functions. In this study, we investigated whether in vivo Treg depletion by treatment with an anti-feline CD25 monoclonal antibody would improve the innate immune response against subcutaneous challenge with Listeria monocytogenes (Lm). Treg depletion resulted in an increased overall number of cells in Lm-draining lymph nodes and increased proliferation of NK and NKT cells in FIV-infected cats. Treg depletion did not normalize expression of perforin or granzyme A by NK and NKT cells, nor did Treg depletion result in improved clearance of Lm. Thus, despite the quantitative improvements in the NK and NKT cell responses to Lm, there was no functional improvement in the early control of Lm. CD1a+ dendritic cell percentages in the lymph nodes of FIV-infected cats were lower than in specific-pathogen-free control cats and failed to upregulate CD80 even when Treg were depleted. Taken together, Treg depletion failed to improve the innate immune response of FIV-infected cats against Lm and this may be due to dendritic cell dysfunction.


2013 ◽  
Vol 153 (1-2) ◽  
pp. 146-152 ◽  
Author(s):  
Laura L. Stoeker ◽  
Elizabeth L. Overman ◽  
Shila K. Nordone ◽  
Adam J. Moeser ◽  
Rita D. Simões ◽  
...  

2001 ◽  
Vol 17 (18) ◽  
pp. 1767-1778 ◽  
Author(s):  
Mary Jo Burkhard ◽  
Candace K. Mathiason ◽  
Todd Bowdre ◽  
Edward A. Hoover

2004 ◽  
Vol 78 (15) ◽  
pp. 8210-8218 ◽  
Author(s):  
Rosemary Stevens ◽  
Kristina E. Howard ◽  
Sushila Nordone ◽  
MaryJo Burkhard ◽  
Gregg A. Dean

ABSTRACT Recombinant Listeria monocytogenes has many attractive characteristics as a vaccine vector against human immunodeficiency virus (HIV). Wild-type and attenuated Listeria strains expressing HIV Gag have been shown to induce long-lived mucosal and systemic T-cell responses in mice. Using the feline immunodeficiency virus (FIV) model of HIV we evaluated recombinant L. monocytogenes in a challenge system. Five cats were immunized with recombinant L. monocytogenes that expresses the FIV Gag and delivers an FIV Env-expressing DNA vaccine (LMgag/pND14-Lc-env). Control cats were either sham immunized or immunized with wild-type L. monocytogenes (LM-wt). At 1 year after vaginal challenge, provirus could not be detected in any of the nine tissues evaluated from cats immunized with the recombinant bacteria but was detected in at least one tissue in 8 of 10 control animals. Virus was isolated from bone marrow of four of five LMgag/pND14-Lc-env-immunized cats by use of a stringent coculture system but required CD8+ T-cell depletion, indicating CD8+ T-cell suppression of virus replication. Control animals had an inverted CD4:CD8 ratio in mesenteric lymph node and were depleted of both CD4+ and CD8+ intestinal epithelial T cells, while LMgag/pND14-Lc-env-immunized animals showed no such abnormalities. Vaginal FIV-specific immunoglobulin A was present at high titer in three LMgag/pND14-Lc-env-immunized cats before challenge and in all five at 1 year postchallenge. This study demonstrates that recombinant L. monocytogenes conferred some control of viral load after vaginal challenge with FIV.


Viruses ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 210 ◽  
Author(s):  
Wendy Sprague ◽  
Ryan Troyer ◽  
Xin Zheng ◽  
Britta Wood ◽  
Martha Macmillan ◽  
...  

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