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Clinical and Diagnostic Laboratory Immunology, July 1998, p. 583-587, Vol. 5, No. 4
Departments of
Neurology,1
Ophthalmology,2 and
Medicine,
Received 7 April 1997/Returned for modification 6 February
1998/Accepted 3 April 1998
Adhesion molecules, which play a major role in lymphocyte
circulation, have not been well characterized in human immunodeficiency virus (HIV) infection. T-lymphocyte populations, including CD3, CD4,
CD28, and adhesion molecules (L selectin, LFA-1, VLA-4, and ICAM-1)
were measured by flow cytometry in a cross-sectional study of 100 HIV-infected and 49 HIV-seronegative adults. HIV-infected adults had
lower numbers of CD3+ lymphocytes expressing L selectin
(P < 0.0001) and VLA-4 (P < 0.01)
and higher numbers of CD3+ lymphocytes expressing
LFA-1bright (P < 0.002) than did
HIV-negative adults. By CD4+-lymphocyte count category
(>500, 200 to 500, or <200 cells/µl), HIV-infected adults with more
advanced disease had lower percentages of CD3+ lymphocytes
expressing L selectin and VLA-4 and higher percentages of
CD3+ lymphocytes expressing LFA-1. The percentages of
CD3+ CD28+ lymphocytes and of CD3+
L selectin+ lymphocytes were positively correlated
(Spearman coefficient = 0.86; P < 0.0001), and the
percentage of CD3+ CD28+ lymphocytes and the
CD3+ LFA-1bright lymphocyte/CD3+
LFA-1dim lymphocyte ratio were negatively correlated
(Spearman coefficient =
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Expression of Adhesion Molecules and CD28 on T Lymphocytes during
Human Immunodeficiency Virus Infection
0.92; P <0.00001). The
results of this study suggest that HIV infection is associated with
altered expression of adhesion molecules.
*
Corresponding author. Mailing address: Ocular
Immunology Service, Suite 700, 550 North Broadway, Baltimore, MD 21205. Phone: (410) 955-3572. Fax: (410) 955-0629. E-mail:
rdsemba{at}welchlink.welch.jhu.edu.
Clinical and Diagnostic Laboratory Immunology, July 1998, p. 583-587, Vol. 5, No. 4
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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