Affiliation:
1. Department of Pathology and Laboratory Medicine1 and
2. Dental Research Center,2 University of North Carolina—Chapel Hill, Chapel Hill, North Carolina 27514
Abstract
ABSTRACT
We have recently found that an extracellular protein, α
1
proteinase inhibitor (α
1
PI; α
1
antitrypsin), is required for in vitro human immunodeficiency virus (HIV) infectivity outcome. We show here in a study of HIV-seropositive patients that decreased viral load is significantly correlated with decreased circulating α
1
PI. In the asymptomatic category of HIV disease, 100% of patients manifest deficient levels of active α
1
PI, a condition known to lead to degenerative lung diseases and a dramatically reduced life span. Further, HIV-associated α
1
PI deficiency is correlated with circulating anti-α
1
PI immunoglobulin G. These results suggest that preventing HIV-associated α
1
PI deficiency may provide a strategic target for preventing HIV-associated pathophysiology.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
15 articles.
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