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aDepartment of Experimental Medicine and Biochemical Science, "Tor Vergata," University Hospital, 00133 Rome, Italy bDepartment of Infectious and Tropical Diseases, University of Rome, "La Sapienza," viale del Policlinico 155, 00161 Rome, Italy cS. Giovanni Hospital, via Amba Aradam 9, 00184, Rome, Italy dIstituto Superiore Sanita, viale Regina Elena 299, Rome, Italy eDepartment of Neuroscience, University of Rome, "Tor Vergata," via Montpellier 1, 00133 Rome, Italy fIRCCS, S. Lucia, via Ardeatina 306, 00179 Rome, Italy gDepartment of Microbiology, Genetics, and Molecular Science, University of Messina, salita Sperone 31, 98166 Messina, Italy
Address for correspondence: Antonio Mastino, Department of Microbiology, Genetics, and Molecular Science, University of Messina, salita Sperone 31, 98166 Messina, Italy. Voice: +39-090-6765198; fax: +39-090-392733. mastino{at}med.uniroma2.it Ann. N.Y. Acad. Sci. 1010: 560-564 (2003).
Although suppression of apoptosis contributes to immune-reconstitution during potent antiretroviral therapy, its relationship with the majors indicators of response to therapy, that is, changes in CD4+ cell counts and in viral loads (VL), is still debated. We extended our previous study by collecting data on the relationships among apoptosis and immunological and virological parameters during a long-term follow-up of HIV patients with an overall positive response to potent antiretroviral therapy. We report results from 15 patients who completed two years of therapy. In a smaller group of patients, we focused our attention on investigating the specific contribution of the CD8+ subset in the overall changes in lymphocyte apoptosis, which occur concomitantly with the response to the therapy. Our data, while again confirming that inhibition of PBMC apoptosis is a phenomenon strictly related to a positive response to potent antiretroviral therapy, suggest that CD4+ cell rescue is not directly dependent on inhibition of CD4+ cell apoptosis but rather on that of the CD8+ subset.
Key Words: CD4+ cells CD8+ cells viral loads antiretroviral therapy
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