E. Mocchegiani et al., Different age-related effects of thymectomy in myasthenia gravis: role of thymoma, zinc, thymulin, IL-2 and IL-6, MECH AGE D, 117(1-3), 2000, pp. 79-91
Different age-related immune pathogenetic mechanisms in myasthenia gravis (
MG) have been suggested because of restoration after thymectomy (Tx) of alt
ered zinc, thymulin (TH) and T-cell subsets exclusively in early-onset pati
ents (younger < 50 years), not in late-onset patients (older > 50 years). I
n this context interleukin-2 (IL-2), interleukin-6 (IL-6) and thymoma are c
rucial because both involved in MG pathogenesis and correlated with acetylc
holine receptors (AchRs) Ab production. Moreover, IL-2 and IL-6 are zinc-de
pendent, are altered in aging and related with zinc and TH age-dependent de
clines. Moreover, zinc is relevant for immune efficiency. In order to confi
rm these different age-related pathogenetic mechanisms further, the role of
thymoma, zinc, TH, IL-2 and IL-6 is studied in MG patients with generalize
d MG with and without thymoma before and 1 month and I year after Tx. The h
igh IL-2, IL-6, zinc, and AChR Ab levels observed before Tx are significant
ly correlated each other in younger MG patients (< 50 years) independently
by thymoma and in older MG patients (> 50 years) with thymoma. No correlati
ons exist in older MG patients without thymoma. Thymulin is not correlated
with other parameters considered to be both in younger and older MG patient
s independently by the thymoma. Thymectomy restores zinc; immune parameters
and AChR Ab are exclusively in the younger group, not in the older one. Th
ese findings suggest that IL-2 and IL-6, via zinc, rather than TH, may be i
nvolved in different age-related pathogenetic mechanisms mainly in early-on
set MG. By contrast, thymoma may be involved in MG etiology in late-onset r
epresenting, as such, a useful discriminant tool for MG etiology between ea
rly and late-onset MG patients. Because autoimmune phenomena may rise in ag
ing, a parallelism with altered immune functions during aging is discussed.
(C) 2000 Elsevier Science Ireland Ltd. All rights reserved.