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Issue 1010 coverApoptosis from Signaling Pathways to Therapeutic Tools Volume 1010 published December 2003
Ann. N.Y. Acad. Sci. 1010: 560–564 (2003). doi: 10.1196/annals.1299.104
Copyright © 2003 by the New York Academy of Sciences
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Articles by GRELLI, S.
Articles by MASTINO, A.
CD4+ Lymphocyte Increases in HIV Patients during Potent Antiretroviral Therapy Are Dependent on Inhibition of CD8+ Cell Apoptosis

SANDRO GRELLIa, GABRIELLA D'ETTOREb, FILIPPO LAURIAc, FRANCESCO MONTELLAc, LOIDE DI TRAGLIAa, CARTESIO D'AGOSTINIa, MIRIAM LICHTNERb, VINCENZO VULLOb, CARTESIO FAVALLIa, STEFANO VELLAd, BEATRICE MACCHIe,f AND ANTONIO MASTINOg

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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