Egemen İDİMAN1, Hakkı BAHAR2, İhsan Şükrü ŞENGÜN1, Göksemin ACAR3, Barış BAKLAN1, Murat SAYAN2, Huriye AYDIN1, Tuncer TOKLU2, Serkan ÖZAKBAŞ1

1Dokuz Eylül Üniversitesi Tıp Fakültesi Nöroloji ABD, İZMİR
2Dokuz Eylül Üniversitesi Tıp Fakültesi Klinik Mikrobiyoloji ABD, İZMİR
3Dokuz Eylül Üniversitesi Tıp Fakültesi Karşıyaka Nöroloji Polikliniği, İZMİR

Keywords: multiple sclerosis, tumour necrosis factor-alpha, disease activity, interferon-beta 1b.

Abstract

Background: A specific marker of disease activity in multiple sclerosis (MS) has notyet been identified. Objective: For this reason this longitudinal prospective study has been carried out in order to determine whether tumour necrosis factor-a (TNF-?) is a predictor of relapse in MS patients and to evaluare the effect of inrerferon ß (IFN-ß) therapy on the TNFa production capacitiy. Material and Methods: Thirty-six relapsing remitting MS (RRMS) patienrs were included in the study and divided into four groups. Group la consisted of 10 relapse presenting patients who were not receiving IFN-ß1b. in Group lb (n- 16), rhe patients were remitting RRMS without any medication. Group lla (n=S), consisted of patients who were under IFN-ß1 b therapy and presented relapse. In Group lıb, there was 5 remitting MS patients receiving IFN-ß1b. Blood samples were collected once a week for about 16 weeks and the samples are stimulated by phytohemagglutinine. The TNF-? production capacitiy of the activated white bfood cells was measured by the ELlSA method. Findings: A total of 139 TNF-? peaks were determined during the follow up and only 9 peaks predicred relapses in 7 RRMS patients. The other 130 TNF-? peaks were possibfy related with infections of the respiraroıy tract (9,2 %), menstrual period (4,6%) and aflegic reactions (0,76 %). No reasons could be determined in the 85% of the 130 peaks. The mean TNF-? production capacity of the Group llb was lower than Group lb (p<0,05). Conclusion: The resufts of this study indicated that TNF-? production capacity was affected by IFN-ß1b treatment, but the periodicaf measurement of TNF-? production capacity ın RRMS patients did not seem to be a sensitive marker in predicting the relapses.