Cellular Immune Activation and Clinical Manifestation of Functional Dyspepsia

2008 ◽  
Vol 46 (09) ◽  
Author(s):  
B Adam ◽  
T Liebregts ◽  
C Bredack ◽  
M Gururatsakul ◽  
G Gerken ◽  
...  
2008 ◽  
Vol 134 (4) ◽  
pp. A-532-A-533
Author(s):  
Tobias Liebregts ◽  
Birgit Adam ◽  
Julia G. Junne ◽  
Montri Gururatsakul ◽  
Alexander Röth ◽  
...  

2009 ◽  
Vol 47 (09) ◽  
Author(s):  
T Liebregts ◽  
B Adam ◽  
M Gururatsakul ◽  
NJ Talley ◽  
G Gerken ◽  
...  

2020 ◽  
Vol 7 (2) ◽  
pp. 191825 ◽  
Author(s):  
James P. Higham ◽  
Christiane Stahl-Hennig ◽  
Michael Heistermann

Studies of large free-ranging mammals incorporating physiological measurements typically require the collection of urine or faecal samples, due to ethical and practical concerns over trapping or darting animals. However, there is a dearth of validated biomarkers of immune activation and inflammation that can be measured non-invasively. We here evaluate the utility of urinary measurements of the soluble form of the urokinase plasminogen activator receptor (suPAR), for use as a health marker in studies of wild large mammals. We investigate how urinary suPAR concentrations change in response to viral infection and surgical trauma (inflammation), comparing it to the measurement of a marker of cellular immune activation, urinary neopterin (uNEO), in captive rhesus macaques. We then test the field utility of urinary suPAR, assessing the effects of soil and faecal contamination, sunlight, storage at different temperatures, freeze–thaw cycles, and lyophilization. We find that suPAR concentrations rise markedly in response to both infection and surgery-associated inflammation, unlike uNEO concentrations, which only rise in response to the former. Our field validation demonstrates that urinary suPAR is reasonably robust to many of the issues associated with field collection, sample processing, and storage, as long as samples can be stored in a freezer. Urinary suPAR is thus a promising biomarker applicable for monitoring various aspects of health in wild primates and potentially also other large mammals.


2020 ◽  
Vol 2 (8) ◽  
pp. 3494-3506
Author(s):  
Dong-qun Liu ◽  
Shuai Lu ◽  
Lun Zhang ◽  
Ling-xiao Zhang ◽  
Mei Ji ◽  
...  

Schematic illustration of the LDH nanoparticle-coated yeast shell vaccine and immune activation.


1988 ◽  
Vol 24 (2) ◽  
pp. 289-289 ◽  
Author(s):  
Dietmarch Fuchs ◽  
Ernst R. Werner ◽  
Manfred P. Dierich ◽  
Helmut Wachter

2019 ◽  
Vol 4 (3) ◽  
pp. 291-300 ◽  
Author(s):  
Agnes Koczo ◽  
Amy Marino ◽  
Arun Jeyabalan ◽  
Uri Elkayam ◽  
Leslie T. Cooper ◽  
...  

2015 ◽  
Vol 112 (15) ◽  
pp. 4719-4724 ◽  
Author(s):  
Anita K. McElroy ◽  
Rama S. Akondy ◽  
Carl W. Davis ◽  
Ali H. Ellebedy ◽  
Aneesh K. Mehta ◽  
...  

Four Ebola patients received care at Emory University Hospital, presenting a unique opportunity to examine the cellular immune responses during acute Ebola virus infection. We found striking activation of both B and T cells in all four patients. Plasmablast frequencies were 10–50% of B cells, compared with less than 1% in healthy individuals. Many of these proliferating plasmablasts were IgG-positive, and this finding coincided with the presence of Ebola virus-specific IgG in the serum. Activated CD4 T cells ranged from 5 to 30%, compared with 1–2% in healthy controls. The most pronounced responses were seen in CD8 T cells, with over 50% of the CD8 T cells expressing markers of activation and proliferation. Taken together, these results suggest that all four patients developed robust immune responses during the acute phase of Ebola virus infection, a finding that would not have been predicted based on our current assumptions about the highly immunosuppressive nature of Ebola virus. Also, quite surprisingly, we found sustained immune activation after the virus was cleared from the plasma, observed most strikingly in the persistence of activated CD8 T cells, even 1 mo after the patients’ discharge from the hospital. These results suggest continued antigen stimulation after resolution of the disease. From these convalescent time points, we identified CD4 and CD8 T-cell responses to several Ebola virus proteins, most notably the viral nucleoprotein. Knowledge of the viral proteins targeted by T cells during natural infection should be useful in designing vaccines against Ebola virus.


2011 ◽  
Vol 47 (1) ◽  
pp. 50-55 ◽  
Author(s):  
A.M. Koorts ◽  
P.F. Levay ◽  
A.N. Hall ◽  
C.F. van der Merwe ◽  
P.J. Becker ◽  
...  

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