scholarly journals Significantly worse survival of patients with NIH-defined chronic graft-versus-host disease and thrombocytopenia or progressive onset type: results of a prospective study

Leukemia ◽  
2011 ◽  
Vol 26 (4) ◽  
pp. 746-756 ◽  
Author(s):  
Z Kuzmina ◽  
S Eder ◽  
A Böhm ◽  
E Pernicka ◽  
L Vormittag ◽  
...  
2018 ◽  
Vol 97 (9) ◽  
pp. 1122-1129 ◽  
Author(s):  
Eva Smith Knutsson ◽  
Yvonne Björk ◽  
Anna-Karin Broman ◽  
Lotti Helström ◽  
Malin Nicklasson ◽  
...  

1980 ◽  
Vol 78 (4) ◽  
pp. 764-771 ◽  
Author(s):  
Roger J. Epstein ◽  
George B. McDonald ◽  
George E. Sale ◽  
Howard M. Shulman ◽  
E.Donnall Thomas

Author(s):  
MM Rivera-Franco ◽  
Eucario León-Rodríguez ◽  
Diana Gómez-Martín

Background: Acute graft-versus-host disease (aGVHD) is an important cause of death following allogeneic hematopoietic stem cell transplantation (allo-HSCT). The association between cholesterol and aGVHD was previously described potentially resulting from pro-inflammatory responses associated with hypercholesterolemia. The aim of this study was to correlate T-cell subsets in donor bone marrow (BM) samples with their levels of cholesterol and associate these results with recipients who developed aGVHD and those who did not. Materials and Methods: A prospective study was performed in 39 donor samples. T-cell subsets were analyzed by flow cytometry. Results: Eleven (28%) donors had hypercholesterolemia. Donor samples with hypercholesterolemia had less Tregs compared to donors with normal levels of cholesterol (22.69 (IQR=30.6) cells/µL vs 52.62 (IQR=44.68) cells/µL, p=0.04). Among all individuals in the cohort, aGVHD was observed in 21%: 36% from donors with hypercholesterolemia versus 14% from donors with normal levels of cholesterol. Conclusion: As we described the association between hypercholesterolemia and diminished Tregs, our results might suggest that normalizing the levels of total cholesterol in the donor, prior performing allo-HSCT, might be an effective approach to diminish the risk of the receptor to develop aGVHD.


Blood ◽  
2010 ◽  
Vol 116 (25) ◽  
pp. 5748-5751 ◽  
Author(s):  
Raewyn Broady ◽  
Jie Yu ◽  
Vickie Chow ◽  
Adisak Tantiworawit ◽  
Christine Kang ◽  
...  

Abstract Studies in mice have shown that proinflammatory Th17 cells can cause acute graft-versus-host disease (aGVHD) related tissue damage; however, whether they play a role in human aGVHD remains unclear. In a prospective study, we measured the proportion of Th17 cells in the blood and skin of patients at the onset of aGVHD. We found no difference in the proportion or amount of IL-17 produced by T cells in the blood of patients with aGVHD (n = 20) compared with time-matched patients without GVHD (n = 14). Moreover, Th17 cells were not increased in the skin of patients with cutaneous aGVHD (n = 7) compared with healthy controls (n = 10). In contrast, we found significantly more interferon-γ–producing T cells in the skin of patients with aGVHD compared with controls. These data support the long-standing paradigm that tissue localized interferon-γ–producing cells are the perpetrators of aGVHD.


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