Sj. Khoury et al., Changes in serum levels of ICAM and TNF-R correlate with disease activity in multiple sclerosis, NEUROLOGY, 53(4), 1999, pp. 758-764
Objective: To study the change in serum levels of soluble intercellular adh
esion molecule 1 (sICAM-1) and soluble tumor necrosis factor receptors (sTN
F-Rs) in MS patients in relation to clinical disease activity and changes o
n brain MRI. Background: Circulating forms of adhesion molecules or soluble
receptors may be released from cells as a consequence of activation and ma
y be useful markers for inflammation. Methods: During a prospective longitu
dinal study over 1 year, 40 patients with MS underwent frequent imaging of
the brain (22 MR images per patient) at the time of blood sampling as well
as monthly neurologic examinations, and scoring on Kurtzke's Expanded Disab
ility Status Scale (EDSS) and ambulation index (Al). Results: Patients with
relapsing-progressive disease had the highest levels of sICAM-1 whereas pa
tients with progressive disease had the highest levels of sTNF-Rs. Fluctuat
ions in sICAM-1 correlated with the occurrence of attacks in patients with
relapsing and relapsing-progressive disease. In patients with relapsing-pro
gressive MS, an increase in sICAM-1 level preceded the appearance of new ga
dolinium (Gd) enhancing lesions an MRI. In patients with progressive diseas
e, an increase in sTNF-R p55 level preceded the appearance of new Gd enhanc
ing lesions on MRI, whereas a decrease in sICAM-1 levels correlated with th
e appearance of new Gd enhancing lesions. Conclusions: These results demons
trate a linkage between sICAM-1 and sTNF-R levels and disease activity in M
S. Furthermore, patients with progressive disease appear to have a differen
t immunologic stage of disease in which immune changes are tightly linked w
ith changes on MRI. The demonstration of a correlation in individual patien
ts between immunologic events and changes in disease activity has implicati
ons for monitoring patients undergoing treatment and for monitoring disease
progression.