AB0007 Comparison of Peripheral Blood Gene Expression Profiles to Phenotype and Treatment Response in the Taser Early Rheumatoid Arthritis Study

2015 ◽  
Vol 74 (Suppl 2) ◽  
pp. 893.2-893
Author(s):  
J. Dale ◽  
J. Nijjar ◽  
J. McClure ◽  
M. McBride ◽  
D. Porter ◽  
...  
2011 ◽  
Vol 1 (1) ◽  
pp. 12 ◽  
Author(s):  
Soumyaroop Bhattacharya ◽  
Shivraj Tyagi ◽  
Sorachai Srisuma ◽  
Dawn L DeMeo ◽  
Steven D Shapiro ◽  
...  

PLoS ONE ◽  
2010 ◽  
Vol 5 (7) ◽  
pp. e11535 ◽  
Author(s):  
Sarah K. Meadows ◽  
Holly K. Dressman ◽  
Pamela Daher ◽  
Heather Himburg ◽  
J. Lauren Russell ◽  
...  

2009 ◽  
Vol 60 (7) ◽  
pp. 2102-2112 ◽  
Author(s):  
Michael G. Barnes ◽  
Alexei A. Grom ◽  
Susan D. Thompson ◽  
Thomas A. Griffin ◽  
Paul Pavlidis ◽  
...  

2022 ◽  
Vol 12 ◽  
Author(s):  
Aafke A. Duizendstra ◽  
Michelle V. van der Grift ◽  
Patrick P. Boor ◽  
Lisanne Noordam ◽  
Robert J. de Knegt ◽  
...  

Spontaneous operational tolerance to the allograft develops in a proportion of liver transplant (LTx) recipients weaned off immunosuppressive drugs (IS). Several previous studies have investigated whether peripheral blood gene expression profiles could identify operational tolerance in LTx recipients. However, the reported gene expression profiles differed greatly amongst studies, which could be caused by inadequate matching of clinical parameters of study groups. Therefore, the purpose of this study was to validate differentially expressed immune system related genes described in previous studies that identified tolerant LTx recipients after IS weaning. Blood was collected of tolerant LTx recipients (TOL), a control group of LTx recipients with regular IS regimen (CTRL), a group of LTx recipients with minimal IS regimen (MIN) and healthy controls (HC), and groups were matched on age, sex, primary disease, time after LTx, and cytomegalovirus serostatus after LTx. Quantitative Polymerase Chain Reaction was used to determine expression of twenty selected genes and transcript variants in PBMCs. Several genes were differentially expressed between TOL and CTRL groups, but none of the selected genes were differentially expressed between HC and TOL. Principal component analysis revealed an IS drug dosage effect on the expression profile of these genes. These data suggest that use of IS profoundly affects gene expression in peripheral blood, and that these genes are not associated with operational tolerance. In addition, expression levels of SLAMF7 and NKG7 were affected by prior cytomegalovirus infection in LTx recipients. In conclusion, we found confounding effects of IS regimen and prior cytomegalovirus infection, on peripheral blood expression of several selected genes that were described as tolerance-associated genes by previous studies.


2005 ◽  
Vol 6 (5) ◽  
pp. 388-397 ◽  
Author(s):  
F M Batliwalla ◽  
E C Baechler ◽  
X Xiao ◽  
W Li ◽  
S Balasubramanian ◽  
...  

2018 ◽  
Author(s):  
Slim Fourati ◽  
Aarthi Talla ◽  
Mehrad Mahmoudian ◽  
Joshua G. Burkhart ◽  
Riku Klén ◽  
...  

AbstractRespiratory viruses are highly infectious; however, the variation of individuals’ physiologic responses to viral exposure is poorly understood. Most studies examining molecular predictors of response focus on late stage predictors, typically near the time of peak symptoms. To determine whether pre- or early post-exposure factors could predict response, we conducted a community-based analysis to identify predictors of resilience or susceptibility to several respiratory viruses (H1N1, H3N2, Rhinovirus, and RSV) using peripheral blood gene expression profiles collected from healthy subjects prior to viral exposure, as well as up to 24 hours following exposure. This analysis revealed that it is possible to construct models predictive of symptoms using profiles even prior to viral exposure. Analysis of predictive gene features revealed little overlap among models; however, in aggregate, these genes were enriched for common pathways. Heme Metabolism, the most significantly enriched pathway, was associated with higher risk of developing symptoms following viral exposure.


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