Im. Medeiros et al., Circulating levels of sTNFR and discrepancy between cytotoxicity and immunoreactivity of TNF-alpha in patients with visceral leishmaniasis, CL MICRO IN, 6(1), 2000, pp. 34-37
Objective To study the influence of soluble tumour necrosis factor (TNF) re
ceptors (sTNFR) on bioactivity; and immunoreactivity of TNF-alpha in patien
ts with visceral leishmaniasis (Kala-azar) and to examine the association b
etween circulating levels of sTNFR type I and type IT with clinical manifes
tations of the disease.
Methods Ten patients with Kala-azar were enrolled. Plasma samples for TNF-a
lpha and sTNFR were obtained on days 0, 7 and 21-28 of antimonial therapy.
Bioactivity of TNF-alpha was measured by cytotoxicity to L-929 cells and im
munoreactivity by enzyme-linked immunosorbent assay (ELISA). sTNFR-I and sT
NFR-II were measured by ELISA.
Results Measured by ELISA, TNF-alpha was detected at baseline in all patien
ts (range from 22.3 to 163 pg/mL) and showed a linear decline over time on
therapy (r = -0.49, P = 0.007). In contrast, when measured by cytotoxicity
assay, TNF-alpha was detected in only one patient at baseline (193 pg/mL) a
nd in four patients at the end of therapy (38.7, 95, 133 and 232 pg/mL) and
there was no linear association between TNF-alpha. and duration of therapy
(r = -0.18, P = 0.45). sTNFR-I and sTNFR-II were detected in all patients
before therapy. There was a strong positive correlation between plasma conc
entrations of sTNFR-I and sTNFR-II (r = 0.8, P = 0.006). Levels of sTNFR-I
and sTNFR-II declined exponentially with time on therapy
Conclusions We concluded that sTNFR-I and sTNFR-II are related to disease a
ctivity in patients with Kala-azar and that these circulating receptors may
interfere with the biological activity of TNF-alpha in patients with Kala-
azar.