Immunological monitoring of disease progression following HIV infectio
n and seroconversion illness, latency and AIDS, not only helps in the
basic investigation of the natural history of the viral infection in m
an, but also can assist in prognosis and treatment of AIDS-defining il
lnesses. However, outside clinical trials, these tests should be selec
ted and used in clinical practice only if they are validated as releva
nt and effective. The absolute CD4+ T-helper lymphocyte count, measure
d by flow cytometry, has emerged as the best available investigation,
but needs care in sampling due to diurnal and circadian rhythms, effec
ts of age, pregnancy, therapy, intercurrent infections and technique.
Sampling should provide a baseline and trends - monthly intervals init
ially, then quarterly in uncomplicated cases. Thresholds may be given
for counts (e.g. 200/mu l) below which prophylaxis against pneumocysti
s pneumonia should be administered, and repeating persistently low cou
nts (e.g. below 50/mu/l) is seldom helpful in practice. Serum levels o
f beta-2 microglobulin, neopterin and immunoglobulins rarely add infor
mation. Physicians and laboratories should have testing guidelines bas
ed on clinical audit of best practice, based in turn on scientific und
erstanding of the immunological processes involved.