MAR, a Novel High-Incidence Rh Antigen Revealing the Existence of an Allelic Sub-System Including C^w (Rh8) and C^x (Rh9) with Exceptional Distribution in the Finnish Population
Abstract:We present new genetic evidence obtained from population studies on Finns and from the studies on Finnish blood donors as well as their selected families using an antibody that defines a novel high-incidence Rh antigen MAR. Anti- MAR antibody shows an antithetical relationship to both anti-C^w and anti-C^x The Rh antigens C^w (RH8) and, more strikingly, C^x (RH9) have each an exceptionally high frequency in Finns. Our studies on their genetic relationship indicate that the three antigens C^w C^x and MAR behave… Show more
“…Anti -MAR was found in a Finnish woman whose red cells were C w + C x + D + C + c − E − e + and who was probably heterozygous DCC w e/DCC x e [388] . Testing of 10 045 Finnish donors revealed 21 MAR -negatives: nine were C w + C x − (probably RHCE * C w /C w ), three were C w − C x + (RHCE * C x /C x ), and nine were C w + C x + ( RHCE * C w /C x ).…”
Section: Mar ( Rh51)mentioning
confidence: 97%
“…antigen MAR [388] . C w and C x result from single nucleotide changes in exon 1 of RHCE (usually RHCE * Ce ) encoding amino acid substitutions in the fi rst extracellular loop: 122A > G, Gln41Arg in C w ; 106G > A, Ala36Thr in C x [389] .…”
“…Anti -MAR was found in a Finnish woman whose red cells were C w + C x + D + C + c − E − e + and who was probably heterozygous DCC w e/DCC x e [388] . Testing of 10 045 Finnish donors revealed 21 MAR -negatives: nine were C w + C x − (probably RHCE * C w /C w ), three were C w − C x + (RHCE * C x /C x ), and nine were C w + C x + ( RHCE * C w /C x ).…”
Section: Mar ( Rh51)mentioning
confidence: 97%
“…antigen MAR [388] . C w and C x result from single nucleotide changes in exon 1 of RHCE (usually RHCE * Ce ) encoding amino acid substitutions in the fi rst extracellular loop: 122A > G, Gln41Arg in C w ; 106G > A, Ala36Thr in C x [389] .…”
“…Family information (lod score = 4.12 at 8 = 0) was also responsible for the elevation of 700048 (FPTT) to RH50, an antigen associated with unusual DCe and Dce (with RH33) complexes, and, in some examples, with a partial RHl (D) antigen (DFR) [56, 571. The high incidence antigen RH51 (MAR) has an antithetical relationship with RH8 (C") and RH9 (C") (lod score = 10.76 at 0 = 0) [58].…”
Since its discovery more than 50 years ago,1,2 the Rh blood group system has continued to challenge, intrigue, tantalize, and (too often) obfuscate blood group serologists. It is fitting that this issue of
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