Circulating interleukin‐6 levels are elevated in adult T‐cell leukaemia/lymphoma patients and correlate with adverse clinical features and survival

We measured the circulating levels of interleukin (IL)‐6 in adult T‐cell leukaemia/lymphoma (ATL) patients using an enzyme‐linked immunosorbent assay. The IL‐6 levels in 59 ATL patients (median 8.2 pg/ml; range < 1.0 to 185.7 pg/ml) were significantly higher than in 30 healthy controls (median &l...

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Published inBritish journal of haematology Vol. 100; no. 1; pp. 129 - 134
Main Authors Yamamura, Masaomi, Yamada, Yasuaki, Momita, Saburou, Kamihira, Shimeru, Tomonaga, Masao
Format Journal Article
LanguageEnglish
Published Oxford, U.K. and Cambridge, USA Blackwell Publishers 01.01.1998
Blackwell
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Summary:We measured the circulating levels of interleukin (IL)‐6 in adult T‐cell leukaemia/lymphoma (ATL) patients using an enzyme‐linked immunosorbent assay. The IL‐6 levels in 59 ATL patients (median 8.2 pg/ml; range < 1.0 to 185.7 pg/ml) were significantly higher than in 30 healthy controls (median < 1.0 pg/ml; range < 1.0 to 3.5 pg/ml) (P < 0.0001) or 32 human T‐lymphotropic virus type‐I (HTLV‐I) carriers (median 4.2 pg/ml; range  < 1.0 to 13.3 pg/ml) (P = 0.002). Among the ATL patients, the IL‐6 levels in the acute‐ or lymphoma‐type patients were significantly higher than those in the chronic‐type patients (P < 0.0001). The IL‐6 levels were also higher in the patients with B symptoms than in those without B symptoms (P = 0.039), and were significantly correlated with increased serum lactate dehydrogenase (LDH) (P = 0.0004) and C‐reactive protein (CRP) (P < 0.0001) and decreased serum albumin (P = 0.0003) values. The patients with elevated IL‐6 levels had inferior overall survival periods compared to those with normal IL‐6 levels (P = 0.025). ATL is a single disease entity, although its clinical features are quite diverse; the increased production of cytokines may cause the diversity of clinical features. The results of our study indicate that IL‐6 is one such cytokine.
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ISSN:0007-1048
1365-2141
DOI:10.1046/j.1365-2141.1998.00538.x