scholarly journals Transgenic mice lacking class I major histocompatibility complex-restricted T cells have delayed viral clearance and increased mortality after influenza virus challenge.

1992 ◽  
Vol 175 (4) ◽  
pp. 1143-1145 ◽  
Author(s):  
B S Bender ◽  
T Croghan ◽  
L Zhang ◽  
P A Small

To investigate the role of CD8+ T lymphocytes in recovery from influenza pneumonia, we used transgenic mice either homozygous (-/-) or heterozygous (+/-) for beta 2-microglobulin (beta 2-M) gene disruption. These mice lack major histocompatibility complex-restricted class I (CD8+) T cells. We found that after challenge with a nonlethal influenza virus, the beta 2-M (-/-) mice had significantly delayed pulmonary viral clearance. Furthermore, after challenge with a more virulent influenza virus, the beta 2-M (-/-) mice had a significantly higher mortality rate than did control mice. Thus, CD8+ T cells are important in recovery from virulent influenza infections, but other host defense mechanisms can clear the respiratory tract of more benign infections.

2004 ◽  
Vol 77 (12) ◽  
pp. 1879-1885 ◽  
Author(s):  
Laila E. Gamadia ◽  
Ester B. Remmerswaal ◽  
Sugianto Surachno ◽  
Neubury M. Lardy ◽  
Pauline M. Wertheim-van Dillen ◽  
...  

1991 ◽  
Vol 174 (4) ◽  
pp. 875-880 ◽  
Author(s):  
M Eichelberger ◽  
W Allan ◽  
M Zijlstra ◽  
R Jaenisch ◽  
P C Doherty

Transgenic mice homozygous for a beta 2-microglobulin (beta 2-m) gene disruption and normal mice that had been treated with a CD8-specific mAb were infected intranasally with an H3N2 influenza A virus. Both groups of CD8T cell-deficient mice eliminated the virus from the infected respiratory tract. Potent CTL activity was detected in lung lavage populations taken from mice with intact CD8+ T cell function, with minimal levels of cytotoxicity being found for inflammatory cells obtained from the antibody-treated and beta 2-m mutant mice. We therefore conclude that cells infected with an influenza A virus can be cleared from the respiratory tract of mice lacking both functional class I major histocompatibility complex (MHC) glycoproteins and class I MHC-restricted, CD8+ effector T cells.


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