scholarly journals Important Role for FcγRIIB on B Lymphocytes for Mucosal Antigen-Induced Tolerance and Foxp3+ Regulatory T Cells

2013 ◽  
Vol 191 (8) ◽  
pp. 4412-4422 ◽  
Author(s):  
Jia-Bin Sun ◽  
Zou Xiang ◽  
Kenneth G. C. Smith ◽  
Jan Holmgren
2009 ◽  
Vol 131 ◽  
pp. S76
Author(s):  
Masato Fujiki ◽  
Samuel Strober ◽  
Olivia Martinez ◽  
Carlos Esquivel ◽  
Sheri Krams

2015 ◽  
Vol 195 (4) ◽  
pp. 1489-1497 ◽  
Author(s):  
Andrew Jones ◽  
Adeleye Opejin ◽  
Jacob G. Henderson ◽  
Cindy Gross ◽  
Rajan Jain ◽  
...  

2019 ◽  
Vol 40 (Supplement_1) ◽  
Author(s):  
T Teszak ◽  
A Assabiny ◽  
A Kiraly ◽  
Z Tarjanyi ◽  
N Parazs ◽  
...  

Abstract Background Cardiac allograft rejection is known to have a profound impact on graft survival and mortality after heart transplant. Previous data on the efficacy of extracorporeal photopheresis (ECP) in the management of cardiac allograft rejection is encouraging. Though, clear evidence on the exact indication and data regarding its effect on distinct lymphocyte subtypes are still lacking. Based on their cytokine production, both helper and cytotoxic T cells can differentiate into either regulatory cells participating in the suppression of rejection or into effector cells responsible for its maintenance. Regulatory T cells are essential for the termination of rejection, while B lymphocytes and natural killer (NK) cells contribute to it. Purpose We aimed to investigate the anti-rejection efficacy and the impact of ECP on peripheral blood lymphocyte subclasses in adult heart transplant recipients. Methods In a retrospective analysis of 12 consecutive patients treated with ECP for cardiac allograft rejection between 2013 and 2019, we examined the grade of rejection in endomyocardial biopsies (EMB) based on the International Society for Heart and Lung Transplantation classification. We analysed the absolute counts and the percentages of helper, cytotoxic and regulatory T cells, B lymphocytes and NK cells with fluorescence activated cell sorting. Measurements were performed both before and after the ECP treatment period. Data values were given as either mean±standard deviation or median [min–max]. Results The patients underwent 26 [2–39] ECP treatments in addition to standard immunosuppressant therapy. Whereas grade 2R cellular rejection was detected in 83% of the cases prior to initiating ECP, none of the examined EMB specimen revealed rejection greater than grade 1R cellular rejection post ECP therapy. The average grade of cellular rejection improved significantly (1.25±0.45 vs. 0.50±0.53; p=0.022). The absolute count and the percentage of helper T cells increased significantly post ECP therapy (0.34 G/l±0.26 G/l vs. 0.51 G/l±0.39 G/l; p=0.018 and 3.43%±2.24% vs. 5.98%±3.64%; p=0.017, respectively). There was also a significant rise in the percentage of cytotoxic T cells (2.33%±1.46% vs. 4.16±2.98%; p=0.027). We noticed an almost significant twofold increase in the percentage of regulatory T cells on completion of the ECP therapy (0.20%±0.22% vs. 0.37%±0.20%; p=0.060). Neither B lymphocyte nor NK cell counts revealed any significant changes. Conclusion ECP was effective in reducing the severity of cardiac allograft rejection episodes. The significant decrease in rejection rates might be indicative of the predominance of anti-inflammatory helper and cytotoxic T cell subpopulations and the increase of regulatory T cell count post ECP therapy. However, discussion of the results are limited by small sample size and the effect of medical therapy on the lymphocytes.


2005 ◽  
Vol 7 (7-8) ◽  
pp. 1023-1032 ◽  
Author(s):  
Ehud Hauben ◽  
Maria Grazia Roncarolo

Allergy ◽  
2013 ◽  
Vol 68 (12) ◽  
pp. 1562-1570 ◽  
Author(s):  
L. W. J. van den Elsen ◽  
L. A. P. M. Meulenbroek ◽  
B. C. A. M. van Esch ◽  
G. A. Hofman ◽  
L. Boon ◽  
...  

2018 ◽  
Author(s):  
Margarita Dudina ◽  
Andrey Savchenko ◽  
Sergey Dogadin ◽  
Alexandr Borisov ◽  
Vladimir Man'kovsky

2005 ◽  
Vol 201 (2) ◽  
pp. 173-179 ◽  
Author(s):  
Agatha Schwarz ◽  
Akira Maeda ◽  
Kerstin Kernebeck ◽  
Harry van Steeg ◽  
Stefan Beissert ◽  
...  

The immunostimulatory cytokine IL-12 is able to antagonize immunosuppression induced by solar/ultraviolet (UV) radiation via yet unknown mechanisms. IL-12 was recently found to induce deoxyribonucleic acid (DNA) repair. UV-induced DNA damage is an important molecular trigger for UV-mediated immunosuppression. Thus, we initiated studies into immune restoration by IL-12 to discern whether its effects are linked to DNA repair. IL-12 prevented both UV-induced suppression of the induction of contact hypersensitivity and the depletion of Langerhans cells, the primary APC of the skin, in wild-type but not in DNA repair-deficient mice. IL-12 did not prevent the development of UV-induced regulatory T cells in DNA repair-deficient mice. In contrast, IL-12 was able to break established UV-induced tolerance and inhibited the activity of regulatory T cells independent of DNA repair. These data identify a new mechanism by which IL-12 can restore immune responses and also demonstrate a link between DNA repair and the prevention of UV-induced immunosuppression by IL-12.


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