Aim: To develop a model of HIV disease progression. Method: Comparativ
e analysis of viral burden and replication between peripheral blood an
d lymphoid organs and of the changes in viral distribution in the lymp
hoid tissue. Results: In early-stage disease HIV-1-infected cells were
sequestered in the lymphoid tissue, and the viral particles were conc
entrated and trapped in the germinal centers. The dichotomy in viral b
urden and viral replication between peripheral blood and lymphoid tiss
ue was related to the histopathologic abnormalities associated with di
fferent stages of disease. Conclusions: These histopathologic abnormal
ities may not only explain the changes in viral distribution observed
in the lymphoid tissue in different stages of the disease, but may als
o reflect different functional states of the immune system during the
progression of HIV-1 infection from early- to late-stage disease.