Detection of Tumour Necrosis Factor from Lipopolysaccharide-Stimulated Human Mononuclear Cells by Enzyme-Linked Immunosorbent Assay and Cytotoxicity Bioassay

1988 ◽  
Vol 27 (2) ◽  
pp. 143-147 ◽  
Author(s):  
A. FOMSGAARD ◽  
H. WORSAAE ◽  
K. BENDTZEN
1990 ◽  
Vol 68 (1) ◽  
pp. 51-55 ◽  
Author(s):  
P. Jeremy McLaughlin ◽  
Ngaire J. Elwood ◽  
Lanny T. Ramadi ◽  
Marie R. Pica ◽  
Ian F. C. McKenzie

2018 ◽  
Vol 19 (3) ◽  
pp. 147032031878574 ◽  
Author(s):  
Wei-wei Chang ◽  
Wei Liang ◽  
Xin-ming Yao ◽  
Liu Zhang ◽  
Li-jun Zhu ◽  
...  

Objective: The objective of this study was to evaluate the expression profile of tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) in patients with diabetic nephropathy (DN). Methods: A total of 126 Chinese subjects were enrolled in this study, including 42 patients with diabetes mellitus (DM), 42 patients with DN and 42 healthy controls. Real-time polymerase chain reaction was performed to analyze levels of TRAIL mRNA in peripheral blood mononuclear cells (PBMCs). Serum levels of soluble TRAIL (sTRAIL) and various cytokines were detected with a commercially available enzyme-linked immunosorbent assay kit. Results: Compared with the control group, the levels of TRAIL mRNA in PBMCs and sTRAIL in sera were both significantly decreased in the DM and DN patients ( P < 0.05). Conversely, levels of interleukin (IL)-1, IL-6, tumour necrosis factor-α and monocyte chemotactic protein-1 were higher in the DN group than in the control group. Serum levels of TRAIL positively correlated with TRAIL mRNA levels in all of the subjects examined ( P < 0.05). Conclusions: These results provide support and a theoretical basis for further research of TRAIL in regard to the pathogenesis of DN.


Rheumatology ◽  
2008 ◽  
Vol 48 (1) ◽  
pp. 32-38 ◽  
Author(s):  
P. F. Sumariwalla ◽  
C. D. Palmer ◽  
L. B. Pickford ◽  
M. Feldmann ◽  
B. M. J. Foxwell ◽  
...  

2003 ◽  
Vol 12 (4) ◽  
pp. 203-207 ◽  
Author(s):  
Alexander L. Pukhalsky ◽  
Galina V. Shmarina ◽  
Maria S. Bliacher ◽  
Irina M. Fedorova ◽  
Anna P. Toptygina ◽  
...  

Background:Immunization with live virus vaccines may cause an immunosuppression with lymphopaenia, impaired cytokine production and defective lymphocyte response to mitogenes. These abnormalities were described in subjects vaccinated against measles. This study was performed to analyse the host immune response related to immunosuppression in subjects vaccinated with live attenuated rubella vaccine.Methods:Eighteen schoolgirls, aged 11-13 years, were vaccinated with live attenuated rubella vaccine Rudivax®. Before immunization, and 7 and 30 days after, peripheral blood was collected. Cellular fractions were subjected to flow cytometric analysis, and the lymphocyte response to phytohaemagglutinin was investigated. Plasma samples were analysed for cytokines (interleukin (IL)-4, IL-10, tumour necrosis factor-α, and interferon-γ) by enzyme-linked immunosorbent assay techniques.Results:On day 7 after vaccination, the number of each lymphocyte subset was decreased; however, only for CD3 and CD4 lymphocytes has a significant reduction been shown. On the contrary, tumour necrosis factor-α and IL-10 levels markedly increased and amounted to its maximum on day 30. Simultaneously, a significant reduction in plasma interferon-γand a profound decrease of the lymphocyte response to phytohaemagglutinin were shown. The changes were accompanied with marked elevation of plasma IL-4.Conclusions:Our data indicate that the vaccination with live attenuated rubella vaccine results in moderate but sustained immune disturbance. The signs of immunosuppression, including defective lymphocyte response to mitogene and impaired cytokine production, may persist for at least 1 month after vaccination.


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