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Blood, 1 April 2007, Vol. 109, No. 7, pp. 2912-2920.
Prepublished online as a Blood First Edition Paper on December 12, 2006; DOI 10.1182/blood-2006-09-047308.
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IMMUNOBIOLOGY
Slow disease progression and robust therapy-mediated CD4+ T-cell recovery are associated with efficient thymopoiesis during HIV-1 infection
Marie-Lise Dion1,2,
Rebeka Bordi1,
Joumana Zeidan1,2,
Robert Asaad3,
Mohammed-Rachid Boulassel4,
Jean-Pierre Routy4,5,
Micheal M. Lederman3,
Rafick-Pierre Sekaly1,2,5,6, and
Remi Cheynier7
1 Laboratoire d'Immunologie, Centre de Recherches du Centre Hospitalier de l'Université de Montréal (CR-CHUM), Hôpital Saint Luc, Montreal, QC, Canada;
2 Department of Microbiology and Immunology, McGill University, Montreal, QC, Canada;
3 Case Western Reserve University Center for AIDS Research, Cleveland, OH;
4 Immunodeficiency Service and Division of Hematology, Royal Victoria Hospital, McGill University Health Centre, McGill University, Montreal, QC, Canada;
5 Institut National de la Santé et de la Recherche Médicale (INSERM) Unité 743, CR-CHUM, Université de Montréal, QC, Canada;
6 Laboratoire d'Immunologie, Département de Microbiologie et Immunologie, Université de Montréal, QC, Canada;
7 Unité des Virus Lents, Institut Pasteur, Paris, France
In chronic HIV infection, most untreated patients lose naive CD4+ and CD8+ T cells, whereas a minority preserve them despite persistent high viremia. Although antiretroviral therapy (ART)mediated viral suppression generally results in a rise of naive and total CD4+ T cells, certain patients experience very little or no T-cell reconstitution. High peripheral T-cell activation has been linked to poor clinical outcomes, interfering with previous evaluations of thymic function in disease progression and therapy-mediated T-cell recovery. To circumvent this, we used the sj/ßTREC ratio, a robust index of thymopoiesis that is independent of peripheral T-cell proliferation, to evaluate the thymic contribution to the preservation and restoration of naive CD4+ T cells. We show that the loss of naive and total CD4+ T cells is the result of or is exacerbated by a sustained thymic defect, whereas efficient thymopoiesis supports naive and total CD4+ T-cell maintenance in slow progressor patients. In ART-treated patients, CD4+ T-cell recovery was associated with the normalization of thymopoiesis, whereas the thymic defect persisted in aviremic patients who failed to recover CD4+ T-cell counts. Overall, we demonstrate that efficient thymopoiesis is key in the natural maintenance and in therapy-mediated recovery of naive and total CD4+ T cells.

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