Alloanti-c in a c-positive, JAL-positive patient

Vox Sang. 2009 Apr;96(3):240-3. doi: 10.1111/j.1423-0410.2008.01135.x. Epub 2008 Dec 5.

Abstract

Background and objectives: In the Rh blood group system, partial D, C, and e antigens are well-known, but a partial c antigen resulting in the production of alloanti-c in a c+ individual is rare. One example of an alloanti-c in a c+ person was an anti-Rh26, which can appear as anti-c, and another was an alloanti-c in a c+ person with a presumed R(1)r phenotype. The finding of an apparent alloanti-c in a transfused c+ patient initiated this investigation.

Materials and methods: Haemagglutination tests, DNA extraction, polymerase chain reaction (PCR)-based assays (PCR-restriction fragment length polymorphism, allele-specific PCR), reticulocyte mRNA extraction, reverse transcriptase (RT)-PCR and sequencing were performed by standard procedures.

Results: Plasma from a 64-year-old African American woman with a wound infection following a mastectomy contained anti-E, anti-S, anti-K, anti-Fy(a) and anti-Jk(b), reacting by the indirect antiglobulin test. In addition, the patient's plasma gave reactions that were consistent with an anti-c, while her pre-transfusion red blood cells typed c+ with some anti-c reagents. These results are consistent with a partial c antigen. The patient's red blood cells also typed V+(W)VS- and JAL+. Analyses of DNA and Rh-transcripts from this patient showed the presence of the following genes: RHD*D, RHD*DAU0, RHCE*Ce and RHCE*ce(S)(340).

Conclusion: The nucleotide 340C>T change in RHCE exon 3 (predicted to encode 114Trp) of the RHCE*ce(S)(340) allele is associated with a JAL+ phenotype and the altered expression of the c, V and VS antigens. This alteration in the c antigen allowed the patient to make an alloanti-c. This case reveals that the RHCE*ce(S)(340) allele encodes a partial c antigen.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Erythrocyte Transfusion
  • Exons*
  • Female
  • Gene Expression Regulation / genetics*
  • Humans
  • Isoantibodies / blood*
  • Isoantibodies / genetics
  • Middle Aged
  • Mutation, Missense*
  • Rh-Hr Blood-Group System / blood*
  • Rh-Hr Blood-Group System / genetics*
  • Surgical Wound Infection / blood
  • Surgical Wound Infection / genetics
  • Surgical Wound Infection / therapy

Substances

  • Isoantibodies
  • RHCE protein, human
  • Rh-Hr Blood-Group System