E. Bergamaschi et al., IMMUNOLOGICAL CHANGES AMONG WORKERS OCCUPATIONALLY EXPOSED TO STYRENE, International archives of occupational and environmental health, 67(3), 1995, pp. 165-171
The functional status of the immune system was investigated in a group
of 71 workers exposed to styrene and in 65 control subjects, recruite
d according to the same selection criteria and comparable as to sex, a
ge, and confounding variables. Air and biological monitoring were used
to characterize styrene exposure (median of the main urinary metaboli
tes in the ''next-morning'' spot samples: 106 mg/g creatinine). Phenot
ypic analysis of peripheral blood lymphocytes (PBL) by automated flow
cytometry revealed a reduced proportion of T lymphocyte subsets (CD3(), CD4(+) and CD4(+) 45(+)), with no changes in CD8(+), and a higher p
roportion of B lymphocytes (CD19(+)) among styrene-exposed workers. Th
e exposed workers showed a higher proportion of activation markers, na
mely DR and interleukin-2 receptors (CD25). Immunoglobulin subclasses
were comparable in the two groups. An increased prevalence of abnormal
ly low values apparent for CD2(+), CD3(+), CD4(+), CD4(+) 45(+) CD11b
subsets among workers exposed to styrene, whereas CD19(+), DR(+) and C
D25(+) showed an increased prevalence of abnormally high values. Natur
al killer-related phenotypes (CD56(+), CD56(+) 16(+), and CD56(+) 16(-
)) were more expressed among styrene workers, with average increase of
30%. However, the frequency distribution of the lytic activity of nat
ural killer cells against K-562 target cells was shifted towards lower
values in the exposed workers as compared to control subjects. Dose-r
esponse relationships between indices of internal dose and prevalence
of abnormal values were detectable for T lymphocyte subsets, NK phenot
ypes, and activation markers. These findings suggest that moderate exp
osure to styrene is associated with an altered distribution of lymphoc
yte subsets. The decreased proportion of T lymphocytes, mainly of T he
lper-inducer cells, could hamper regulatory functions, thus suggesting
a negative modulation by styrene exposure. Since a proper balance bet
ween immunocycte subsets is important for immunological responses, suc
h changes should be regarded as adverse effects.