Rb. Moss et al., Phenotypic analysis of human immunodeficiency virus (HIV) type 1 cell-mediated immune responses after treatment with an HIV-1 immunogen, J INFEC DIS, 180(3), 1999, pp. 641-648
It was hypothesized that immune recognition could be stimulated with combin
ed immune-based and potent antiviral drug therapies. This study examined hu
man immunodeficiency virus type 1 (HIV-1)-specific lymphocyte proliferation
before and after treatment with an inactivated HIV-1 immunogen in 15 chron
ically infected HIV-1 seropositive subjects. Lymphocyte proliferation to th
e immunizing antigen (gp120-depleted HIV-1; P<.001), purified native p24 (P
<.001), and recombinant p24 (P <.05) increased after treatment with the HI
V-specific immune-based therapy. By HIV-1 antigen-specific flow cytometry,
T helper CD4 lymphocytes, CD8 lymphocytes, and NK cells tall P<.001) were t
he predominant cell types proliferating in vitro after treatment. Additiona
l phenotyping of proliferating cells revealed predominantly CD4 and CD8 mem
ory (both P<.001) phenotypes. This study supports the concept that in vitro
lymphocyte proliferation to HIV-1 antigens, augmented after treatment with
an inactivated HIV-1 immunogen, involves primarily CD4 and CD8 cell memory
immune responses.