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Journal of Virology, November 2001, p. 10843-10855, Vol. 75, No. 22
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.22.10843-10855.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Exogenous Interleukin-2 Administration Corrects the Cell Cycle Perturbation of Lymphocytes from Human Immunodeficiency Virus-Infected Individuals

Mirko Paiardini,1,2 Domenico Galati,3 Barbara Cervasi,1,2 Giuseppe Cannavo,3 Luca Galluzzi,2 Maria Montroni,4 Denise Guetard,5 Mauro Magnani,2 Giuseppe Piedimonte,3 and Guido Silvestri1,*

Vaccine Research Center and Division of Infectious Diseases, Department of Medicine, Emory University, Atlanta, Georgia1; Istituto di Chimica Biologica "G. Fornaini," Universitá di Urbino, Urbino,2 Dipartimento di Patologia Generale, Malattie Infettive ed Ispezione degli Alimenti, Facoltá di Medicina Veterinaria, and Dipartimento di Igiene, Medicia Preventiva e Sanitá Pubblica, Facoltá di Medicina e Chirurgia, Universitá degli Studi di Messina, Messina,3 and Servizio di Immunologia Clinica, Facoltá di Medicina e Chirurgia, Universitá di Ancona, Ancona,4 Italy; and Unite de Oncologie Virale and Département SIDA et Retrovirus, Institut Pasteur, Paris, France5

Received 21 May 2001/Accepted 30 July 2001

Human immunodeficiency virus (HIV)-induced immunodeficiency is characterized by progressive loss of CD4+ T cells associated with functional abnormalities of the surviving lymphocytes. Increased susceptibility to apoptosis and loss of proper cell cycle control can be observed in lymphocytes from HIV-infected individuals and may contribute to the lymphocyte dysfunction of AIDS patients. To better understand the relation between T-cell activation, apoptosis, and cell cycle perturbation, we studied the effect of exogenous interleukin-2 (IL-2) administration on the intracellular turnover of phase-dependent proteins. Circulating T cells from HIV-infected patients display a marked discrepancy between a metabolic profile typical of G0 and a pattern of expression of phase-dependent proteins that indicates a more-advanced position within the cell cycle. This discrepancy is enhanced by in vitro activation with ConA and ultimately results in a marked increase of apoptotic events. Conversely, treatment of lymphocytes with IL-2 alone restores the phase-specific pattern of expression of cell cycle-dependent proteins and is associated with low levels of apoptosis. Interestingly, exogenous IL-2 administration normalizes the overall intracellular protein turnover, as measured by protein synthesis, half-life of newly synthesised proteins, and total protein ubiquitination, thus providing a possible explanation for the effect of IL-2 on the intracellular kinetics of cell cycle-dependent proteins. The beneficial effect of IL-2 administration is consistent with the possibility of defective IL-2 function in vivo, which is confirmed by the observation that lymphocytes from HIV-infected patients show abnormal endogenous IL-2 paracrine/autocrine function upon in vitro mitogen stimulation. Overall these results confirm that perturbation of cell cycle control contributes to HIV-related lymphocyte dysfunction and, by showing that IL-2 administration can revert this perturbation, suggest a new mechanism of action of IL-2 therapy in HIV-infected patients.


* Corresponding author. Mailing address: Vaccine Research Center and Division of Infectious Diseases, Dept. of Medicine, Emory University, 954 Gatewood Rd. NE, Atlanta, GA 30329. Phone: (404) 712-8113. Fax: (404) 727-8199. E-mail: gsilves{at}rmy.emory.edu.


Journal of Virology, November 2001, p. 10843-10855, Vol. 75, No. 22
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.22.10843-10855.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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