Persistent Abnormalities in Lymphoid Tissues of Human Immunodeficiency Virus–Infected Patients Successfully Treated with Highly Active Antiretroviral Therapy (original) (raw)

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Reprints or correspondence: Dr. Timothy W. Schacker, Dept. of Medicine, University of Minnesota, MMC 250, 516 Delaware St., Minneapolis, MN 55455 (schacker@lenti.med.umn.edu)

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7Hospital Clinic, University Hospital, Barcelona, Spain;

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7Hospital Clinic, University Hospital, Barcelona, Spain;

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6Centrum Diagnostyki Therapy AIDS, Warsaw, Poland;

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6Centrum Diagnostyki Therapy AIDS, Warsaw, Poland;

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5Northwestern University Medical School, Chicago, Illinois;

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8International Antiviral Therapy Evaluation Centre, Amsterdam, The Netherlands

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5Northwestern University Medical School, Chicago, Illinois;

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Revision received:

31 May 2002

Published:

15 October 2002

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Timothy W. Schacker, Phuong L. Nguyen, Esteban Martinez, Cavan Reilly, Jose M. Gatell, Andrzej Horban, Elzbieta Bakowska, Baiba Berzins, Remko van Leeuwen, Steven Wolinsky, Ashley T. Haase, Robert L. Murphy, Persistent Abnormalities in Lymphoid Tissues of Human Immunodeficiency Virus–Infected Patients Successfully Treated with Highly Active Antiretroviral Therapy, The Journal of Infectious Diseases, Volume 186, Issue 8, 15 October 2002, Pages 1092–1097, https://doi.org/10.1086/343802
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Abstract

Effective highly active antiretroviral therapy (HAART) for human immunodeficiency virus type 1 is associated with virus suppression and immune reconstitution. However, in some patients, this reconstitution is partial or incomplete because CD4+ cell counts do not increase significantly. This may be due to damage in the microenvironment of lymphoid tissues (LTs), where CD4+ T cells reside. To test this hypothesis, LT samples were obtained from 23 patients enrolled in a prospective trial that compared 3 different HAART regimens. Analysis of LT architecture and CD4+ T cells populations revealed abnormalities in 100% of the LT samples, especially in the follicles, with 43% showing absence, 14% showing regression, and 43% showing hyperplasia. CD4+ T cell populations were abnormal in 16 (89%) of 18 tissue samples, with 7 (39%) of 18 decreased by >50% of normal levels. These data are consistent with the hypothesis that persistent abnormalities in the microenvironment can influence immune reconstitution and document persistent LT abnormalities with HAART not detected by measures of peripheral CD4+ T cell count

© 2002 by the Infectious Diseases Society of America

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