Abstract
In the human Rh blood group system, c is, after D, the most immunogenic antigen. The background of a new partial c phenotype (D(c)), identified on the RBCs of two unrelated white persons, was studied. This was done by analyzing the reactivity of the RBCs from the donors with anti-c reagents, by performing sequence analysis, and by carrying out transduction studies. Serologic results suggested the existence of a new partial c phenotype. Genomic DNA and cDNA analysis revealed a normal RHCe allele, a normal RHD allele, and an RHD allele that carried two point mutations: 307T>C and 329T>C (the latter known to be associated with the DVII, Tar-positive phenotype). No normal RHc allele was found. Thus, it was most likely that c is encoded by the mutated RHD allele (phenotype DD(c)CCee). Indeed, subsequent transduction of K562 erythroleukemic cells with an RHD cDNA carrying the 307T>C point mutation (leading to S103P) resulted in the expression of c. In the human Rh system, P103 is involved in the expression of c. Moreover, c can be expressed in vivo on the D polypeptide
| Original language | English |
|---|---|
| Pages (from-to) | 1136-1142 |
| Journal | Transfusion |
| Volume | 41 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 2001 |
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