scholarly journals IFN-Stimulated Gene 15 Is an Alarmin that Boosts the CTL Response via an Innate, NK Cell–Dependent Route

2020 ◽  
Vol 204 (8) ◽  
pp. 2110-2121 ◽  
Author(s):  
Victoria Iglesias-Guimarais ◽  
Tomasz Ahrends ◽  
Evert de Vries ◽  
Klaus-Peter Knobeloch ◽  
Andriy Volkov ◽  
...  
Keyword(s):  
Nk Cell ◽  
2006 ◽  
Vol 4 (14) ◽  
pp. 533-543 ◽  
Author(s):  
Dominik Wodarz ◽  
Sophie Sierro ◽  
Paul Klenerman

Upon acute viral infection, a typical cytotoxic T lymphocyte (CTL) response is characterized by a phase of expansion and contraction after which it settles at a relatively stable memory level. Recently, experimental data from mice infected with murine cytomegalovirus (MCMV) showed different and unusual dynamics. After acute infection had resolved, some antigen specific CTL started to expand over time despite the fact that no replicative virus was detectable. This phenomenon has been termed as ‘CTL memory inflation’. In order to examine the dynamics of this system further, we developed a mathematical model analysing the impact of innate and adaptive immune responses. According to this model, a potentially important contributor to CTL inflation is competition between the specific CTL response and an innate natural killer (NK) cell response. Inflation occurs most readily if the NK cell response is more efficient than the CTL at reducing virus load during acute infection, but thereafter maintains a chronic virus load which is sufficient to induce CTL proliferation. The model further suggests that weaker NK cell mediated protection can correlate with more pronounced CTL inflation dynamics over time. We present experimental data from mice infected with MCMV which are consistent with the theoretical predictions. This model provides valuable information and may help to explain the inflation of CMV specific CD8+T cells seen in humans as they age.


2000 ◽  
Vol 74 (15) ◽  
pp. 7032-7038 ◽  
Author(s):  
Craig D. Peacock ◽  
Meei Y. Lin ◽  
John R. Ortaldo ◽  
Raymond M. Welsh

ABSTRACT The role of negatively signaling NK cell receptors of the Ly49 family on the specificity of the acute CD8+ cytotoxic T-lymphocyte (CTL) response was investigated in lymphocytic choriomeningitis virus (LCMV)-infected C57BL/6 mice. Activated CD8+ T cells coexpressing Ly49G2 expanded during LCMV infection, and T-cell receptor analyses by flow cytometry and CDR3 spectratyping revealed a unique polyclonal T-cell population in the Ly49G2+ fraction. These cells lysed syngeneic targets infected with LCMV or coated with two of three LCMV immunodominant peptides examined. Transfection of these sensitive targets with H2Dd, a ligand for Ly49G2, inhibited lysis. This was reversed by antibody to Ly49G2, indicating effective negative signaling. LCMV characteristically induces an anti-H2dallospecific T-cell response that includes T-cell clones cross-reactive between allogeneic and LCMV-infected syngeneic targets. The CD8+ Ly49G2+ population mediated no allospecific killing, nor was any NK-like killing observed against YAC-1 cells. This study shows that CD8+ Ly49G2+cells participate in the virus-induced CTL response but lyse a more restricted range of targets than the rest of the virus-induced CTL population.


Author(s):  
Leilani M. Chirino ◽  
Suresh Kumar ◽  
Mariko Okumura ◽  
David E. Sterner ◽  
Michael Mattern ◽  
...  

Author(s):  
Anthony G. Mansour ◽  
Run Xiao ◽  
Stephen M Bergin ◽  
Wei Huang ◽  
Logan A. Chrislip ◽  
...  

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