Evaluation of the Pathogenesis of Decreasing CD4+T Cell Counts in Human Immunodeficiency Virus Type 1–Infected Patients Receiving Successfully Suppressive Antiretroviral Therapy
Author(s) -
Elizabeth NiesKraske,
Timothy W. Schacker,
David Condoluci,
Jan M. Orenstein,
Jason M. Brenchley,
Cecil H. Fox,
Marybeth Daucher,
Robin Dewar,
Elizabeth Urban,
Brenna J. Hill,
Javier Guenaga,
Shelley Hoover,
Frank Maldarelli,
Claire W. Hallahan,
Judith Horn,
Shyamasundaran Kottilil,
TaeWook Chun,
Marlene Folino,
Sara Palmer,
Ann Wiegand,
Marie A. O’Shea,
Julia A. Metcalf,
Daniel C. Douek,
John M. Coffin,
Ashley T. Haase,
Anthony S. Fauci,
Mark Dybul
Publication year - 2009
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/598980
Subject(s) - viremia , didanosine , immunology , viral load , t cell , antiretroviral therapy , virology , pathogenesis , virus , lentivirus , viral disease , viral replication , medicine , biology , immune system
Most human immunodeficiency virus (HIV)-infected individuals experience increases in peripheral CD4(+) T cell counts with suppressive antiretroviral therapy (ART) that achieves plasma HIV RNA levels that are less than the limit of detection. However, some individuals experience decreasing CD4(+) T cell counts despite suppression of plasma viremia. We evaluated 4 patients with a history of CD4(+) T cell decline despite successfully suppressive ART, from a median of 719 cells/mm(3) (range, 360-1141 cells/mm(3)) to 227 cells/mm(3) (range, 174-311 cells/mm(3)) over a period of 18-24 months; 3 of the patients were receiving tenofovir and didanosine, which may have contributed to this decrease. There was no evidence of HIV replication, nor of antiretroviral drug resistance in the blood or lymphoid tissue, or increased proliferation or decreased thymic production of naive CD4(+) T cells. All 4 patients had significant fibrosis of the T cell zone of lymphoid tissue, which appeared to be an important factor in the failure to reconstitute T cells.
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