Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasia
- PMID: 111729
Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasia
Abstract
Myeloid metaplasia is a clonal disease of the marrow pluripotent stem cell in which a constant cytogenetic abnormality could result in an altered antigenic characteristic of hematopoietic cells. A 57-yr-old man who had acquired myeloid metaplasia at age 37 was noted to be Rh negative, although blood typing at age 33 was Rh positive. His erythrocytes reacted with anti-c and anti-e, typical for an Rh negative individual. Analysis of 11 metaphase bone marrow cells by G-banding revealed 46 chromosomes with a consistent anomaly in 100% of cells involving chromosomes 1 and 13. The changes were consistent with a reciprocal translocation, with break points at approximately 1p32 and 13q22, although break points at 1p13 and 13q14 were also possible. Since previous cytogenetic data have localized the Rh gene to the short arm of chromosome 1, our data indicate the Rh gene lies within the segment u13 leads to 1p32. Serum of this patient had circulating anti-D and anti-C antibodies. Consequently, this patient lost immunologic tolerance to a "self antigen" after losing the ability to express this antigen.
Similar articles
-
Mapping human autosomes: evidence supporting assignment of rhesus to the short arm of chromosome No. 1.Science. 1974 Mar 8;183(4128):966-8. doi: 10.1126/science.183.4128.966. Science. 1974. PMID: 4204206
-
An identical translocation between chromosome 1 and 7 in three patients with myelofibrosis and myeloid metaplasia.Br J Haematol. 1980 Apr;44(4):569-75. doi: 10.1111/j.1365-2141.1980.tb08711.x. Br J Haematol. 1980. PMID: 7378317
-
Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia.Cancer Genet Cytogenet. 2002 Aug;137(1):68-71. doi: 10.1016/s0165-4608(02)00554-x. Cancer Genet Cytogenet. 2002. PMID: 12377417
-
Cytogenetic and molecular genetic abnormalities in agnogenic myeloid metaplasia.Semin Oncol. 2005 Aug;32(4):359-64. doi: 10.1053/j.seminoncol.2005.04.007. Semin Oncol. 2005. PMID: 16202681 Review.
-
Clonal analysis of agnogenic myeloid metaplasia.Leuk Lymphoma. 1992 Dec;8(6):459-64. doi: 10.3109/10428199209051028. Leuk Lymphoma. 1992. PMID: 1363649 Review.
Cited by
-
Somatic mosaicisms of chromosome 1 at two different stages of ontogenetic development detected by Rh blood group discrepancies.Haematologica. 2019 Mar;104(3):632-638. doi: 10.3324/haematol.2018.201293. Epub 2018 Sep 20. Haematologica. 2019. PMID: 30237270 Free PMC article.
-
Frameshift variations in the RHD coding sequence: Molecular mechanisms permitting protein expression.Transfusion. 2020 Nov;60(11):2737-2744. doi: 10.1111/trf.16123. Epub 2020 Oct 9. Transfusion. 2020. PMID: 33037655 Free PMC article. Review. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources