t helper response
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Author(s):  
Aïda Meghraoui-Kheddar ◽  
Mehdi Sellami ◽  
Sandra Audonnet ◽  
Moncef Guenounou ◽  
Richard Le Naour

2008 ◽  
Vol 68 (3) ◽  
pp. 893-900 ◽  
Author(s):  
Marjolein M. Lauwen ◽  
Sander Zwaveling ◽  
Linda de Quartel ◽  
S. Carmela Ferreira Mota ◽  
Janine A.C. Grashorn ◽  
...  

2007 ◽  
Vol 133 (6) ◽  
pp. 2010-2018 ◽  
Author(s):  
Christiane Wiegard ◽  
Petra Wolint ◽  
Christian Frenzel ◽  
Uta Cheruti ◽  
Edgar Schmitt ◽  
...  

2001 ◽  
Vol 8 (6) ◽  
pp. 1225-1230 ◽  
Author(s):  
Giampiero Piccinini ◽  
Giuditta Comolli ◽  
Emilia Genini ◽  
Daniele Lilleri ◽  
Roberto Gulminetti ◽  
...  

ABSTRACT Evaluation of human cytomegalovirus (HCMV)-specific T-helper immunity could contribute in optimizing anti-HCMV therapy in human immunodeficiency virus (HIV)-infected patients. Testin the lymphoproliferative response (LPR) is the standard technique used to evaluate T-helper response, but its use in the routine diagnostic laboratory setting can be problematic. The most promising new alternative technique is the determination of HCMV-specific CD4+ T-cell frequency by flow cytometry detection of intracellular cytokine production after short-term antigen-specific activation of peripheral blood mononuclear cells. HCMV-specific LPR and CD4+ T-cell frequency were compared in a group of 78 blood samples from 65 HIV-infected patients. The results showed concordance in 80.7% of samples. In addition, comparative analysis of sequential blood samples from 13 HIV-infected patients showed that while in about half of patients the T-helper HCMV-specific immune response remained stable during highly active antiretroviral therapy (HAART), in the other half declining levels of the HCMV-specific CD4+-mediated immune response were determined by either one or both assays. In conclusion, our data suggest that the determination of HCMV-specific CD4+ T-cell frequency can be considered a valuable alternative to the LPR test for the detection of HCMV-specific T-helper response in HIV-infected patients. It could facilitate wider screening of anti-HCMV T-helper activity in HIV-infected patients, with potential benefits for clinicians in deciding strategies of discontinuation or maintenance of anti-HCMV therapy.


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