Jm. Pascale et al., IMMUNOLOGICAL MARKERS OF DISEASE PROGRESSION IN PATIENTS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS, Clinical and diagnostic laboratory immunology, 4(4), 1997, pp. 474-477
Identification of inexpensive and technically simple immunological tes
ts useful in predicting the progression to AIDS in human immunodeficie
ncy virus (HIV)-infected patients would be especially welcome in devel
oping countries, in which 80% of the HIV-infected patients reside and
health budgets are low, In the current study, we evaluated CD4(+) and
total lymphocyte counts and the concentrations in serum of beta(2)-mic
roglobulin, p24 antigen, and immunoglobulin A (IgA) as predictors of d
isease progression in 74 Panamanian HIV-positive patients and 50 HIV-n
egative healthy individuals, Total lymphocyte and CD4(+)-cell counts f
or AIDS patients (1,451 +/- 811 cells/mu l, P < 0.001, and 238 +/- 392
cells/mu l, P < 0.0001, respectively) and asymptomatic patients (2,39
3 +/- 664 cells/mu l, P > 0.05, and 784 +/- 475 cells/mu l, P < 0.001,
respectively) were lower than those observed for healthy subjects (2,
596 +/- 631 cells/mu l and 1,120 +/- 296 cells/mu l, respectively), Th
e levels of beta(2)-microglobulin and IgA in serum were significantly
elevated in patients with AIDS (5.7 +/- 3.6 mg/liter, P < 0.0001, and
541 +/- 265 mg/dl, P < 0.0001, respectively) and asymptomatic infected
subjects (3.4 +/- 2.1 mg/liter, P = 0.001, and 436 +/- 216 mg/dl, P <
0.0001, respectively) compared with the levels in healthy subjects (2
.2 +/- 0.7 mg/liter and 204 +/- 113 mg/dl, respectively). Nonstatistic
ally significant differences (P > 0.05) for concentrations of p24 anti
gen between asymptomatic infected patients (29 +/- 13 pg/ml) and AIDS
patients (40 +/- 23 mu g/ml) were observed, Total lymphocyte counts of
1,750 cells/mu l or less, CD4 counts of 200 cells/mu l or less, beta(
2)-microglobulin concentrations in serum of 4 mg/liter or higher, conc
entrations of IgA in serum of 450 mg/dl or higher, and the presence in
serum of p24 antigen were correlated with elevated risks for developi
ng AIDS, monitoring both total lymphocytes and beta(2)-microglobulin i
dentified 91% of the AIDS patients; these assays may allow reductions
in the annual number of CD4(+)-cell evaluations and the costs associat
ed with monitoring the immune status of HIV-positive patients.