scholarly journals Role of Integrin αE(CD103)β7 for Tissue-Specific Epidermal Localization of CD8+ T Lymphocytes

2001 ◽  
Vol 117 (3) ◽  
pp. 569-575 ◽  
Author(s):  
Katrin Pauls ◽  
Margarete Schön ◽  
Robert C. Kubitza ◽  
Bernhard Homey ◽  
Andrea Wiesenborn ◽  
...  
2009 ◽  
Vol 69 (7) ◽  
pp. 3069-3076 ◽  
Author(s):  
Joachim H. Maxeiner ◽  
Roman Karwot ◽  
Kerstin Sauer ◽  
Petra Scholtes ◽  
Ildiko Boross ◽  
...  

2010 ◽  
Vol 87 (4) ◽  
pp. 424-431 ◽  
Author(s):  
Elisa Bordón ◽  
Luis Alberto Henríquez-Hernández ◽  
Pedro Carlos Lara ◽  
Beatriz Pinar ◽  
Carlos Rodríguez-Gallego ◽  
...  

EBioMedicine ◽  
2017 ◽  
Vol 20 ◽  
pp. 202-216 ◽  
Author(s):  
Laura B. Talarico ◽  
Juan P. Batalle ◽  
Alana B. Byrne ◽  
Jorge M. Brahamian ◽  
Adrián Ferretti ◽  
...  

2008 ◽  
Vol 26 (15_suppl) ◽  
pp. 11024-11024
Author(s):  
A. Lacko ◽  
I. Gisterek ◽  
R. Matkowski ◽  
A. Halon ◽  
K. Szewczyk ◽  
...  

2013 ◽  
Vol 8 (3) ◽  
pp. 226-239 ◽  
Author(s):  
Vladimira Durmanova ◽  
Monika Homolova ◽  
Juraj Drobny ◽  
Ivana Shawkatova ◽  
Milan Buc

AbstractPregnancy loss (abortion) and pre-eclampsia represent the most common disorders in pregnant women. Besides infection, there are anatomical, endocrinological, genetic and immunological factors that can induce pregnancy disorders. Because the exact mechanisms of physiological pregnancy maintenance are still not clearly understood, the search for genes and proteins fulfilling this role is still in progress. One of the immune molecules that plays a beneficial role in pregnancy is the nonclassical HLA-G molecule. The molecule is mainly expressed on trophoblast cells in the foetal placenta and induces the immune tolerance of the foetus via its interaction with inhibitory receptors on maternal NK cells and CD8+ T lymphocytes. In relation to pregnancy disorders, associations between HLA-G polymorphism, HLA-G level and HLA-G function were described. Thus, the HLA-G molecule can be used as a new diagnostic marker and, potentially, for the future therapy of pregnancy disorders.


2018 ◽  
Vol 33 (suppl_1) ◽  
pp. i409-i409
Author(s):  
Agnes Mooslechner ◽  
Alexander Kirsch ◽  
Katharina Artinger ◽  
Ida Aringer ◽  
Foteini Moschovaki-Filippidou ◽  
...  

2015 ◽  
pp. 211-218
Author(s):  
Giuseppe Pantaleo ◽  
Cecilia Graziosi ◽  
Luca Butini ◽  
Anthony S. Fauci

Blood ◽  
2004 ◽  
Vol 103 (3) ◽  
pp. 1026-1029 ◽  
Author(s):  
Randy S. Longman ◽  
Andrew H. Talal ◽  
Ira M. Jacobson ◽  
Matthew L. Albert ◽  
Charles M. Rice

Abstract The absence of expanded numbers of hepatitis C virus (HCV)-reactive CD8+ T lymphocytes (CTLs) in patients chronically infected with HCV has led to the investigation of dendritic cell (DC) function in this population as a potential cause for this defect. Several studies have shown evidence for impaired monocyte-derived DCs in chronically infected patients. As it is difficult to reconcile these data with the fact that patients with chronic HCV are immune competent, we re-evaluated this finding, carefully assessing phenotypic markers and functional activity of patient DCs as compared with noninfected controls. In contrast to these prior studies, DCs from 13 of 13 chronic HCV patients expressed typical maturation markers. These mature DCs were capable of priming allogeneic T lymphocytes, as well as stimulating influenza-specific memory T cells. This finding is consistent with clinical and immunologic data that the deficit in the patient's immune repertoire is HCV-specific and suggests that refined models are required for understanding the role of DCs in HCV pathogenesis. (Blood. 2004;103:1026-1029)


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