scholarly journals A 37-year-old woman with refractory coeliac disease type II disease treated by stem cell transplantation

2015 ◽  
pp. bcr2015209363 ◽  
Author(s):  
Pardeep Kumar Maheshwari ◽  
Iain Feeley ◽  
Hilary Oleary ◽  
Carol Goulding
2021 ◽  
Vol 22 (12) ◽  
pp. 6595
Author(s):  
Michiko Horiguchi ◽  
Yuya Turudome ◽  
Kentaro Ushijima

In cases of patients with rapidly progressive diabetes mellitus (DM), autologous stem cell transplantation is considered as one of the regenerative treatments. However, whether the effects of autonomous stem cell transplantation on DM patients are equivalent to transplantation of stem cells derived from healthy persons is unclear. This study revealed that adipose-derived mesenchymal stem cells (ADSC) derived from type II DM patients had lower transplantation efficiency, proliferation potency, and stemness than those derived from healthy persons, leading to a tendency to induce apoptotic cell death. To address this issue, we conducted a cyclopedic mRNA analysis using a next-generation sequencer and identified G6PC3 and IGF1, genes related to the FoxO signaling pathway, as the genes responsible for lower performance. Moreover, it was demonstrated that the lower transplantation efficiency of ADSCs derived from type II DM patients might be improved by knocking down both G6PC3 and IGF1 genes. This study clarified the difference in transplantation efficiency between ADSCs derived from type II DM patients and those derived from healthy persons and the genes responsible for the lower performance of the former. These results can provide a new strategy for stabilizing the quality of stem cells and improving the therapeutic effects of regenerative treatments on autonomous stem cell transplantation in patients with DM.


2010 ◽  
Vol 51 (6) ◽  
pp. 793-794 ◽  
Author(s):  
J Hans Hoekstra ◽  
Jacqueline J Groot-Loonen ◽  
Annemieke van der Weij ◽  
Peter M Hoogerbrugge ◽  
Yvonne Kooy ◽  
...  

2010 ◽  
Vol 138 (5) ◽  
pp. S-303-S-304
Author(s):  
Greetje J. Tack ◽  
Marielle J. Wondergem ◽  
Abdul Al-Toma ◽  
Wieke H. Verbeek ◽  
Alexander Schmittel ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Gaurang Modi ◽  
Sandip Shah ◽  
Irappa Madabhavi ◽  
Harsha Panchal ◽  
Apurva Patel ◽  
...  

The most frequent form of congenital dyserythropoiesis (CDA) is congenital dyserythropoietic anemia II (CDA II). CDA II is a rare genetic anemia in humans, inherited in an autosomally recessive mode, characterized by hepatosplenomegaly normocytic anemia and hemolytic jaundice. Patients are usually transfusion-independent except in severe type. We are here reporting a case of severe transfusion-dependent type II congenital dyserythropoietic anemia in a 5-year-old patient who has undergone allogeneic hematopoietic stem cell transplantation (HSCT) at our bone marrow transplantation centre. Patient has had up until now more than 14 mL/kg/month of packed cell volume (PCV), which he required every 15 to 20 days to maintain his hemoglobin of 10 gm/dL and hematocrit of 30%. His pre-HSCT serum ferritin was 1500 ng/mL and he was on iron chelating therapy. Donor was HLA identical sibling (younger brother). The preparative regimen used was busulfan, cyclophosphamide, and antithymocyte globulin (Thymoglobulin). Cyclosporine and short-term methotrexate were used for graft versus host disease (GVHD) prophylaxis. Engraftment of donor cells was quick and the posttransplant course was uneventful. The patient is presently alive and doing well and he has been transfusion-independent for the past 33 months after HSCT.


Gut ◽  
2012 ◽  
Vol 62 (4) ◽  
pp. 509-519 ◽  
Author(s):  
Frederike Schmitz ◽  
Jennifer M L Tjon ◽  
Yuching Lai ◽  
Allan Thompson ◽  
Yvonne Kooy-Winkelaar ◽  
...  

2013 ◽  
Vol 61 (4) ◽  
pp. 743-745 ◽  
Author(s):  
M. Braun ◽  
M. Wölfl ◽  
V. Wiegering ◽  
B. Winkler ◽  
K. Ertan ◽  
...  

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