We have recently found that an extracellular protein, alpha (1) proteinase
inhibitor (alpha 1PI; alpha (1) antitrypsin), is required for in vitro huma
n immunodeficiency virus (HIV) infectivity outcome. We show here in a study
of HIV-seropositive patients that decreased viral load is significantly co
rrelated with decreased circulating alpha 1PI. In the asymptomatic category
of HIV disease, 100% of patients manifest deficient levels of active alpha
1PI, a condition known to lead to degenerative lung diseases and a dramati
cally reduced life span. Further, HIV-associated alpha 1PI deficiency is co
rrelated with circulating anti-alpha 1PI immunoglobulin G. These results su
ggest that preventing HIV-associated alpha 1PI deficiency may provide a str
ategic target for preventing HIV-associated pathophysiology.