P. Ruiz et al., PERIPHERAL HUMAN T-LYMPHOCYTE MAINTENANCE OF IMMUNE FUNCTIONAL-CAPACITY AND PHENOTYPIC CHARACTERISTICS FOLLOWING IN-VIVO COCAINE EXPOSURE, Clinical immunology and immunopathology (Print), 88(3), 1998, pp. 271-276
The effects of cocaine exposure upon the host's immune response is equ
ivocal since a variety of studies have generated conflicting conclusio
ns, often as the result of differences between in vitro and/or animal
models and the actual conditions experienced in humans who are acutely
abusing this drug. To further address this issue, we have studied a g
roup of patients who were positive for cocaine or cocaine metabolites
and we evaluated a variety of functional parameters of T-lymphocytes a
nd other peripheral lymphoid cell populations, as well as immunophenot
ypic characteristics of these cells. When compared to normal controls
and patients who were negative for cocaine, we found that the cocaine-
positive patients had T-cell functional assays which were essentially
normal, with the exception of a slight depression in PHA stimulation L
ikewise, the immunophenotype of the peripheral blood lymphocytic popul
ations showed normal percentages and numbers of their T cell subsets (
CD4, CD8), NK cells, and B cells. Multicolor flow cytometry analysis r
evealed no difference in T cell subpopulations positive for the ''memo
ry'' marker, CD62L, No correlation could be established between levels
of cocaine or cocaine metabolites and any phenotypic, demographic, or
functional parameter, In summary, these results demonstrate that indi
viduals acutely exposed to cocaine do not show markedly altered T cell
function or fluctuations in phenotypically identified cell population
s. These studies imply that acute cocaine exposure does not predispose
individuals to grossly apparent immunosuppression. However, the possi
bility that subtle, transient, or more specific changes in the immune
system may be incurred by use of cocaine, particularly with chronic ex
posure, remains to be determined. (C) 1998 Academic Press.