Literature DB >> 10753854

Survival of donor cells 25 years after intrauterine transfusion.

H E Viëtor1, E Hallensleben, S P van Bree, E M van der Meer, S E Kaal, J Bennebroek-Gravenhorst, H H Kanhai, A Brand, F H Claas.   

Abstract

Persistence of donor leukocytes in the circulation of recipients of intrauterine transfusion (IUT) has been observed up to 5 years after birth. The aim of this study was to determine whether transfusions with nonirradiated, nonleukocyte-depleted donor blood during the fetal period resulted in long-term immunomodulation of the recipient. Twenty-four surviving IUT recipients between 1966 and 1976 were tested for autoimmune disease and autoantibodies at follow-up. Ten had sex-mismatched donors and were therefore informative for chimerism studies using fluorescence in situ hybridization (FISH). Seven female recipients could be tested for chimerism using a Y- chromosome-specific polymerase chain reaction (PCR) because they received at least 1 IUT from a male donor. Nine recipients could be studied for cytotoxic T-lymphocyte precursor (CTLp) and helper T-lymphocyte precursor (HTLp) frequencies because the original donors were available for testing. All surviving IUT recipients were in good health at the time of the examination, and routine laboratory testing revealed no abnormalities. None of the IUT recipients were chimeric as determined by FISH analysis, but Y-chromosome-specific sequences were detected by PCR in 6 of the 7 women. However, the CTLp and HTLp frequencies of the IUT recipients against the donors were comparable to those of the controls. The current study provides evidence that IUT can result in the persistence of donor cells in the recipient for a period longer than 20 years but that it is not associated with immunotolerance or with signs of chronic antigenic stimulation. (Blood. 2000;95:2709-2714)

Entities:  

Mesh:

Year:  2000        PMID: 10753854

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  6 in total

1.  Can post-mortem blood be used for DNA profiling after peri-mortem blood transfusion?

Authors:  E A M Graham; M Tsokos; G N Rutty
Journal:  Int J Legal Med       Date:  2005-12-10       Impact factor: 2.686

2.  Long-term feto-maternal microchimerism: nature's hidden clue for alternative donor hematopoietic cell transplantation?

Authors:  Tatsuo Ichinohe; Etsuko Maruya; Hiroh Saji
Journal:  Int J Hematol       Date:  2002-10       Impact factor: 2.490

Review 3.  Transfusion-associated microchimerism: the hybrid within.

Authors:  Evan M Bloch; Rachael P Jackman; Tzong-Hae Lee; Michael P Busch
Journal:  Transfus Med Rev       Date:  2012-10-24

4.  Absence of transfusion-associated microchimerism in pediatric and adult recipients of leukoreduced and gamma-irradiated blood components.

Authors:  Rosa Sanchez; Tzong-Hae Lee; Li Wen; Leilani Montalvo; Cathy Schechterly; Camilla Colvin; Harvey J Alter; Naomi L C Luban; Michael P Busch
Journal:  Transfusion       Date:  2011-10-07       Impact factor: 3.157

5.  Lack of Evidence That Male Fetal Microchimerism is Present in Endometriosis.

Authors:  Amelie Fassbender; Maria Debiec-Rychter; Rieta Van Bree; Joris Robert Vermeesch; Christel Meuleman; Carla Tomassetti; Karen Peeraer; Thomas D'Hooghe; Dan I Lebovic
Journal:  Reprod Sci       Date:  2015-03-05       Impact factor: 3.060

Review 6.  Microchimerism in children with rheumatic disorders: what does it mean?

Authors:  Ann M Reed
Journal:  Curr Rheumatol Rep       Date:  2003-12       Impact factor: 4.592

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.