Expression and quantitative variation of the low-incidence blood group antigen He on some S-s- red cells

被引:14
作者
Reid, ME
Storry, JR
Ralph, H
Blumenfeld, OO
Huang, CH
机构
[1] ALBERT EINSTEIN COLL MED,DEPT BIOCHEM,BRONX,NY 10467
[2] NEW YORK BLOOD CTR,LINDSLEY F KIMBALL RES INST,NEW YORK,NY 10021
关键词
D O I
10.1046/j.1537-2995.1996.36896374376.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Red cells devoid of glycophorin B (GPB)-borne S, s, and U antigens are classified as an S-s-U- or S-s-U variant (U+(var)) and can arise from deletion and nondeletion genetic backgrounds. In nondeletion forms of S-s-U-, little information is available on whether the altered GPB gene (GYPB) is expressed in red cells. Study Design and Methods: Red cells classified as S-s-U- or S-s-U+(var) were tested with anti-U, anti-U/GPB, anti-He, and anti-N by hemagglutination. Selected samples were tested by flow cytometry, immunoblotting, and polymerase chain reaction amplification using allele-specific primers. Results: He (MNS6) was found on 23 percent (20/87) of samples. These and another 21 of the 87 samples were agglutinated by an anti-U/GPB reagent; this indicated that approximately 50 percent of S-s- samples possessed GPB variants. The strength of He varied among the samples. Genomic polymerase chain reaction with allele-specific primers showed the presence of expected DNA GPB-like products encoding He. Immunoblotting showed that He was carried on a membrane component with a relative molecular mass indistinguishable from that of GPB. Conclusion: The finding of He on S-s- red cells provides direct evidence for the presence of an altered form of GPB in red cells previously thought to be devoid of this glycophorin. Quantitative variation in He antigen expression was observed in a subset of S-s- red cells.
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页码:719 / 724
页数:6
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共 28 条
[21]   Optimizing exchange transfusion for patients with severe Babesia divergens babesiosis: Therapeutically-Rational Exchange (T-REX) of M antigen-negative and/or S antigen-negative red blood cells should be evaluated now [J].
Jajosky, R. P. ;
Jajosky, A. N. ;
Jajosky, P. G. .
TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2019, 26 (01) :76-79
[22]   Gene expression pattern of some classes of cytochrome P-450 and glutathione S-transferase enzymes in differentiated hepatocytes-like cells from menstrual blood stem cells [J].
Aida Esmaeili-Rad ;
Sayeh Khanjani ;
Hamidreza Vaziri ;
Somaieh Kazemnejad .
In Vitro Cellular & Developmental Biology - Animal, 2015, 51 :530-538
[23]   Gene expression pattern of some classes of cytochrome P-450 and glutathione S-transferase enzymes in differentiated hepatocytes-like cells from menstrual blood stem cells [J].
Esmaeili-Rad, Aida ;
Khanjani, Sayeh ;
Vaziri, Hamidreza ;
Kazemnejad, Somaieh .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2015, 51 (05) :530-538
[24]   Immunocompetence and reproductive characteristics of Campbell’s dwarf hamster males selected for low and high humoral immune response on sheep red blood cells (SRBC): Testing the immunocompetence handicap hypothesis [J].
K. A. Rogovin ;
A. M. Khrushcheva ;
O. N. Shekarova ;
A. V. Bushuev ;
O. V. Sokolova ;
N. Yu. Vasilieva .
Biology Bulletin Reviews, 2015, 5 (3) :249-258
[25]   CD2 antigen expression on leukemic cells as a predictor of event-free survival after chemotherapy for T-lineage acute lymphoblastic leukemia: A Children's Cancer Group study [J].
Uckun, FM ;
Steinherz, PG ;
Sather, H ;
Trigg, M ;
Arthur, D ;
Tubergen, D ;
Gaynon, P ;
Reaman, G .
BLOOD, 1996, 88 (11) :4288-4295
[26]   Quantitative measurement of protein S gene expression by reverse transcription-competitive PCR method; Determination of mRNA level in fractionated human peripheral blood cells and various cultured cell lines. [J].
Okamoto, Y ;
Hara, Y ;
Ishikawa, S ;
Nishida, M .
BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL, 1998, 44 (05) :877-885