Cj. Cohen et al., LACK OF EFFECT OF CIMETIDINE ON LYMPHOCYTE SUBSETS IN PATIENTS INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1, Clinical infectious diseases, 23(5), 1996, pp. 1049-1054
Cimetidine, widely used for peptic ulcer disease, blocks type 2 histam
ine receptors present on immune cells, including T cells, B cells, and
monocytes, As an earlier published study showed evidence of increases
in CD4 cell counts due to this drug, we conducted a randomized, place
bo-controlled, 8-week trial of oral cimetidine (400 mg po t.i.d.) in a
study involving 182 patients infected with human immunodeficiency vir
us (HIV), Overall, cimetidine-treated patients had a decline in CD4(+)
cell counts that was no different from the decline for placebo-treate
d persons, neither during the first 8 weeks of the trial (mean drop, 7
.1% [standard error, 12.1-1.8] vs. 6.7% [standard error, 11.6-1.5]) no
r during the subsequent 8 weeks of open-label administration of cimeti
dine. No differences were evident between the treatment groups in term
s of the percentage reactive to p24 antigen at baseline, and p24 antig
en concentrations did not change from baseline to the end of week 8. I
n summary, cimetidine is well tolerated by HIV-infected individuals bu
t alters neither CD4(+) cell counts nor at least one quantitative meas
ure of viral load, HIV p24 antigen levels.