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3+ 4/2002 - Společnost pro pojivové tkáně

3+ 4/2002 - Společnost pro pojivové tkáně

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suggestion that CH are absorbed from GIT<br />

as peptides.<br />

Methods: For this study CH was prepared<br />

from rat skin by enzymatic digestion.<br />

Molecular mass of obtained peptides was<br />

500 – 3500.<br />

CH (1.0 µg) was then mixed with 50<br />

mg incomplete Freud's adjuvant and a<br />

sheep was immunized. Serum (20 ml<br />

blood) was firstly collected 20 days after<br />

the last booster. Antibodies titer was determined<br />

by ELISA. Specific antibodies were<br />

isolated by CNBr-activated Sepharose 4B<br />

chromatography. From various tissue samples<br />

(liver, oesophagus, kidney, sternum,<br />

legjoints) of mice fed with CH for 11 days<br />

(10 mg/10 g body weight daily) frozen sections<br />

were stained with primary antibodies<br />

in the first step and in the second diluted<br />

FITC-conjugated rabbit anti-sheep IgG was<br />

applied. Samples from the same organs<br />

were used for EM evaluation.<br />

Results: mouse liver after feeding with<br />

CH exhibited a massive fluorescence also in<br />

the cytoplasm of hepatocytes at the level of<br />

central vein lobules. Positive findings were<br />

ascertained further in joints. Articular cartilage<br />

possessed ring shaped fluorescent signals<br />

at the region of chondrocyte extracellular<br />

matrix boundary. Analogous findings<br />

were observed in sternum. EM evaluation<br />

using immuno-gold method for CH demonstration<br />

confirmed findings at the light microscopy<br />

level.<br />

Discussion: Presented findings clearly<br />

show that peptides containing the respective<br />

antigenic determinants cross the GIT<br />

wall. Elements which are able to transfer<br />

peptides and <strong>pro</strong>teins across the gastrointestinal<br />

wall and bring them to the lymphatic<br />

and blood capillaries are EAF<br />

(epithelium associated with follicules). Massive<br />

fluorescence in cytoplasma in mouse<br />

liver indicates that CH is collected at first in<br />

liver. Further the authors suggest that the<br />

presence of gold-labeled antibodies to CH<br />

as well as finding of immunof1uorescence<br />

in cytoplasma is very important for the elucidation<br />

of mode of action of CH in diseased<br />

human beings.<br />

SERUM LEVELS OF SVCAM-1,<br />

SICAM-1 AND GELATINASES A AND B<br />

AS POSSIBLE PREDICTORS OF THE<br />

OUTCOME OF RHEUMATIC ARTHRITIS<br />

J. Šovíčková, S. Macháček, J. Gatherová<br />

Institute of Rheumatology, Na Slupi 4, 128 50 Prague 2,<br />

Czech republic<br />

Introduction: There is a need to find<br />

predictive markers to judge <strong>pro</strong>gress of<br />

rheumatic diseases as e.g. rheumatoid<br />

arthritis. Recently it was found that interaction<br />

of adhesive molecules ICAM-1 or<br />

VCAM-1on the cell surface can initiate<br />

gelatinases expression. They are capable to<br />

degrade extracellular matrix.<br />

Methods: We follow the levels of<br />

sICAM-1, sVCAM-1, and gelatinases A and B<br />

in the sera of 60 patients with early<br />

rheumatoid arthritis and compared them<br />

with the levels of C-reactive <strong>pro</strong>tein and<br />

disease score DAS and radiografic score<br />

according to Larsen. The levels of sICAM-1;<br />

sVCAM-1, both gelatinases, and CRP were<br />

assesed in 6 month intervals, the DAS and<br />

radiografic score in 12 month intervals<br />

within two years.<br />

Results: We found that in all intervals<br />

sICAM-1 correlated with sVCAM-1 (0.3147<<br />

r s

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