JAC Advance Access originally published online on December 12, 2002
Journal of Antimicrobial Chemotherapy (2003) 51, 1-4
© 2003 The British Society for Antimicrobial Chemotherapy
Immune reconstitution with antiretroviral therapies in chronic HIV-1 infection
Christoph G. Lange1,* and
Michael M. Lederman2
1 Medical Clinic, Research Center Borstel, Medical University of Lübeck, Parkallee 35, 23845 Borstel, Germany; 2 Center for AIDS Research, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, OH, USA
Keywords: HIV, HAART, immune reconstitution
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Introduction
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Human immunodeficiency virus 1 (HIV-1) infection is characterized
by a progressive decline in both function and number of CD4+
T-lymphocytes secondary to ongoing viral replication. Without
intervention, this ultimately leads to the development of the
Acquired Immunodeficiency Syndrome (AIDS) that places persons
at risk for the acquisition of opportunistic infections and
neoplasms.
1 In recent years, reconstitution of the immune system
of HIV-1-infected patients has been achieved by suppression
of HIV-1 replication through antiretroviral therapies (ART),
resulting in a dramatic decline in HIV-1-related morbidity and
mortality.
2 Whereas in the short term, restoration of numbers
of circulating CD4+ T-cells seems to largely protect persons
from opportunistic infections, it is less clear that functional
immune responses can be fully restored particularly in persons
with advanced stages of HIV infection. Recent findings from
clinical trials and epidemiological studies suggest that the
timing of treatment initiation is a major determinant of the
capacity of the
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Restoration of the circulating CD4+ T-cell pool on ART
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Restoration of the immune phenotype on ART is often incomplete, particularly if treatment initiation is delayed
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Functional immune restoration depends upon timing of treatment initiation
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How much immune reconstitution is enough?
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Restoration of HIV-1-specific immunity on ART
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Conclusions
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Acknowledgements
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