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Posterske teme Poster topics - Biochemia Medica

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P17-6 Imunologija<br />

serumima dobivene su vrijednosti kod nefelometrijskog<br />

određivanja za IgG 6,4%, IgA 1,9%, IgM 1,24%, a kod imunoturbidimetrijskog<br />

određivanja za IgG 4,3%, IgA 1,3%,<br />

IgM 2,9%. Usporedbom rezultata dobivenih na nefelometru<br />

i biokemijskom analizatoru dobiveni su koefi cijenti korelacije<br />

za IgG r=0,9882; za IgA r=0,9953; za IgM r=0,9933.<br />

Određivanjem imunoglobulina imunonefelometrijski i<br />

imunoturbidimetrijski dobili smo rezultate koji su usporedivi<br />

i ukazuju da su obje metode prihvatljive za rutinski<br />

rad.<br />

E-mail: bmladina@net.hr<br />

P17-7<br />

Dokazivanje plazmatskih proupalnih<br />

citokina i čimbenika rasta na mikročipu<br />

Predragović T 1 , Kozmar A 1 , Benjak V 2 , Jadranka S 3 , Malenica B 1<br />

1 Zavod za imunologiju, Klinički zavod za laboratorijsku dijagnostiku,<br />

Klinički bolnički centar Zagreb, Zagreb, Hrvatska<br />

2 Klinika za pedijatriju, Klinički bolnički centar Zagreb, Zagreb, Hrvatska<br />

3 Centar za genomiku, Klinički zavod za laboratorijsku dijagnostiku,<br />

Klinički bolnički centar Zagreb, Zagreb, Hrvatska<br />

Citokini su važni biološki čimbenici u regulaciji imunoreaktivnosti<br />

i patofi ziologiji raznih infektivnih bolesti, te<br />

bolesti uzrokovanih upalom, poremećajem staničnog rasta<br />

i stvaranja novih krvnih žila. Mjerenjem pojedinačnih<br />

citokina enzimoimunotestom (ELISA) opažena je povišena<br />

koncentracija različitih proupalnih citokina u plazmi<br />

bolesnika s teškim infekcijama, autoimunim bolestima i<br />

nekim karcinomima. Otuda i zanimanje za ispitivanje moguće<br />

dijagnostičke i prognostičke vrijednosti proupalnih<br />

citokina u raznim bolestima. Nove tehnologije, kao što su<br />

mikrokuglice ili mikročipovi s monoklonskim antitijelima<br />

specifi čnim za razne citokine, omogućuju istodobno dokazivanje<br />

više različitih citokina u istom uzorku plazme.<br />

U istraživanju smo rabili mikročip s dvanaest različitih citokina<br />

i čimbenika rasta. Koncentraciju citokina u plazmi<br />

odredili smo u 11 novorođenčadi s različitim bakterijskim<br />

infekcijama, 7 novorođenčadi s raznim urođenim grješkama<br />

bez popratne infekcije, te u 7 odraslih bolesnika s<br />

raznim histološkim tipovima i lokalizacijama karcinoma.<br />

Razinu proupalnih citokina odredili smo mikročipom koji<br />

omogućuje istodobno mjerenje IL-2, IL-4, IL-6, IL-8, IL-10,<br />

VEGF, IFN-gama, TNF-alfa, IL-1 alfa, IL-1 beta, MCP-1 i EGF.<br />

Koncentracija kemokina IL-8 i MCP-1 povišena je u svih ispitanika.<br />

Povišena je i koncentracija IL-6 i TNF-alfa u 75%<br />

by immunoturbidimetric determination were IgG 4.4%,<br />

IgA 4.2% and IgM 5.1%. Determination of inaccuracy with<br />

control serum by immunonephelometric method yielded<br />

the following values: IgG 6.4%, IgA 1.9% and IgM 1.24%,<br />

and with immunoturbidimetric method IgG 4.3%, IgA<br />

1.3% and IgM 2.9%. Comparison of the results obtained<br />

by these two analyses (nephelometer and biochemistry<br />

analyzer) produced the following correlation coeffi cients:<br />

IgG r=0.9882, IgA r=0.9953 and IgM r=0.9933. The results<br />

obtained by immunonephelometric and immunoturbidimetric<br />

assays show that both methods are comparable<br />

and acceptable for routine work.<br />

E-mail: bmladina@net.hr<br />

P17-7<br />

Immunology<br />

Detection of plasma proinfl ammatory<br />

cytokines and growth factors by biochip array<br />

Predragović T 1 , Kozmar A 1 , Benjak V 2 , Jadranka S 3 , Malenica B 1<br />

1Laboratory of Immunology, Clinical Institute of Laboratory Diagnosis,<br />

Zagreb University Hospital Center, Zagreb, Croatia<br />

2University Department of Pediatrics, Zagreb University Hospital Center,<br />

Zagreb, Croatia<br />

3Laboratory of Genomics, Clinical Institute of Laboratory Diagnosis,<br />

Zagreb University Hospital Center, Zagreb, Croatia<br />

Cytokines are major biologic factors in the modulation of<br />

immune responses and in the pathophysiology of various<br />

infections and diseases related to infl ammation, growth<br />

deregulation and vascular remodeling. Determination of<br />

a single cytokine by ELISA has shown elevated concentrations<br />

of various proinfl ammatory cytokines in plasma of<br />

patients with serious infections, autoimmune diseases<br />

and cancer. These data motivated further investigations<br />

to determine the possible diagnostic and prognostic<br />

value of proinfl ammatory cytokine measurement. New<br />

technologies such as microbeads or biochip array platform<br />

with monoclonals specifi c for various cytokines allow<br />

for simultaneous detection of multiple cytokines in<br />

the same plasma sample. In this study, we used a biochip<br />

array platform for proinfl ammatory cytokine determination<br />

in the plasma of newborn infants and adults with<br />

cancer. Plasma cytokine levels were determined in 11<br />

newborns with various bacterial infections, 7 infants<br />

without infection, and 7 adults with diff erent histologic<br />

types and localization of cancer. Plasma cytokine levels<br />

were evaluated by biochip array for simultaneous detection<br />

of IL-2, IL-4, IL-6, IL-8, IL-10, VEGF, IFN-gamma, TNFalfa,<br />

IL-1 alfa, IL-1 beta, MCP-1 and EGF. Plasma levels of<br />

IL-8 and MCP-1 chemokines were elevated in all patients.<br />

<strong>Biochemia</strong> <strong>Medica</strong> 2006;16(Suppl 1):S1–S268<br />

S195

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