Nadir CD4 T Cell Count as Predictor and High CD4 T Cell Intrinsic Apoptosis as Final Mechanism of Poor CD4 T Cell Recovery in Virologically Suppressed HIV-Infected Patients: Clinical Implications
Background. Although antiretroviral therapy improves immune response, some human immunodeficiency virus-infected patients present unsatisfactory CD4 T cell recovery despite achieving viral suppression, resulting in increased morbidity and mortality. Methods. Cross-sectional, case-control study to characterize the mechanism and to identify predictive factors of poor immune response. We included 230 patients who were receiving highly active antiretroviral therapy and who had a viral load <50 copies/mL for >2 years; 95 were "discordant" (case patients; CD4 T cell count always <350 cells/mu L), and 135 were "concordant" (control subjects). Activation markers, CD4 T cell death (necrosis, intrinsic apoptosis, and extrinsic apoptosis), and caspase-3 were measured. Clinical parameters, particularly antiretroviral combinations, were correlated with immune recovery. Results. Discordant patients showed higher levels of activation markers, mainly in CD4 T cells (P < .001), and higher rates of spontaneous cell death (P < .001). Rates of activation and rates of CD4 T cell death (mainly by intrinsic apoptosis) were the best predictive factors for immune recovery, along with nadir CD4 T cell count. Patients who were receiving a protease inhibitor-based regimen were more likely to be discordant and showed higher rates of activation (P = . 011), higher rates of CD4 T cell death (P = . 033), and a lower nadir CD4 T cell count (P < .001). Multivariate analysis, however, ruled out any effect of protease inhibitors on immune recovery. No differences were observed between the use of tenofovir-emtricitabine (Truvada) and the use of abacavir-lamivudine (Kivexa). Conclusions. CD4 T cell apoptosis by the intrinsic pathway represents the determinant mechanism of the unsatisfactory immune recovery and should be targeted to manage therapy for discordant patients. The predictive value of low nadir CD4 T cell count for a poor immune recovery led us to consider starting antiretroviral therapy earlier. No differences were observed among antiretrovirals in terms of immune recovery.
机构:
Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
Teigen, Nickolas
Liff, Ingrid
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Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
Liff, Ingrid
Reimers, Laura
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Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
Reimers, Laura
Miraz, Maria
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Bronx Lebanon Hosp Ctr, Bronx, NY 10456 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
Miraz, Maria
Sutton, Desmond
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Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
Sutton, Desmond
Wright, Rodney
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Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol & Womens Hlth, Bronx, NY 10467 USA
机构:
Kumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, JapanKumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, Japan
Sakai, Keiko
Gatanaga, Hiroyuki
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Kumamoto Univ, Div Infect Dis, Ctr AIDS Res, Kumamoto 8600811, Japan
Int Med Ctr Japan, AIDS Clin Ctr, Shinjuku Ku, Tokyo 1628655, JapanKumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, Japan
Gatanaga, Hiroyuki
Takata, Hiroshi
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Kumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, JapanKumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, Japan
Takata, Hiroshi
Oka, Shinichi
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Kumamoto Univ, Div Infect Dis, Ctr AIDS Res, Kumamoto 8600811, Japan
Int Med Ctr Japan, AIDS Clin Ctr, Shinjuku Ku, Tokyo 1628655, JapanKumamoto Univ, Div Viral Immunol, Ctr AIDS Res, Kumamoto 8600811, Japan