Literature DB >> 7222561

Lewis phenotype of erythrocytes and Leb-active glycolipid in serum of pregnant women.

L Hammar, S Månsson, T Rohr, M A Chester, V Ginsburg, A Lundblad, D Zopf.   

Abstract

In an attempt to provide an explanation for the previously reported effect of pregnancy on the Lewis phenotype of erythrocytes, the level of Leb-active glycolipid in serum was compared with the reactions of erythrocytes, using samples obtained from 73 nonpregnant women, 74 women at the time of delivery, and 2 women at weekly intervals during their pregnancy. In this Swedish population, the frequency of the Le(a--b-) blood group increased from 11% in nonpregnant women to 36% in women at the time of delivery. Among Le(a--b+) women of all ABO groups, those who were A1 most often became (Leb-) during pregnancy. The change in phenotype occurred as early as the 24th week of gestation; the Leb antigen was again detectable within 6 weeks after delivery. The concentration of Leb glycolipid in serum, as measured by radioimmunoassay, decreased only slightly during pregnancy. The repartition of glycolipids, secondary to the increased ratio of lipoprotein to red cell mass that occurs during pregnancy, may account for the relative lack of Lewis glycolipid on erythrocytes.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 7222561     DOI: 10.1111/j.1423-0410.1981.tb00665.x

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  12 in total

1.  [Clinical value of the CA 19-9 tumor marker with special reference to the Lewis phenotype].

Authors:  G Kolb; F Safi; K Beckh; H G Beger
Journal:  Med Klin (Munich)       Date:  1997-04-15

2.  Immunochemical and immunohistological expression of Lewis histo-blood group antigens in small intestine including individuals of the Le(a+b+) and Le(a-b-) nonsecretor phenotypes.

Authors:  S M Henry; B E Samuelsson; R Oriol
Journal:  Glycoconj J       Date:  1994-12       Impact factor: 2.916

3.  Abnormal blood rheology and chronic low grade inflammation: possible risk factors for accelerated atherosclerosis and coronary artery disease in Lewis negative subjects.

Authors:  Tamas Alexy; Eszter Pais; Rosalinda B Wenby; Wendy J Mack; Howard N Hodis; Naoko Kono; Jun Wang; Oguz K Baskurt; Timothy C Fisher; Herbert J Meiselman
Journal:  Atherosclerosis       Date:  2015-01-21       Impact factor: 5.162

4.  The Lewis blood group system in liver transplantation.

Authors:  G Ramsey; J Wolford; D J Boczkowski; F W Cornell; P Larson; T E Starzl
Journal:  Transplant Proc       Date:  1987-12       Impact factor: 1.066

5.  Editorial: Role of Y Chromosome in Molecular Anthropology, Forensics, and Genetic Genealogy.

Authors:  Sibte Hadi; Jun Yao; Atif Adnan
Journal:  Front Genet       Date:  2022-06-09       Impact factor: 4.772

6.  Helicobacter pylori expresses a complex surface carbohydrate, Lewis X.

Authors:  R Sherburne; D E Taylor
Journal:  Infect Immun       Date:  1995-12       Impact factor: 3.441

7.  Detection of urothelial Lewis antigens with monoclonal antibodies.

Authors:  C Limas
Journal:  Am J Pathol       Date:  1986-12       Impact factor: 4.307

Review 8.  Human milk oligosaccharides and Lewis blood group: individual high-throughput sample profiling to enhance conclusions from functional studies.

Authors:  Dennis Blank; Viktoria Dotz; Rudolf Geyer; Clemens Kunz
Journal:  Adv Nutr       Date:  2012-05-01       Impact factor: 8.701

9.  Lewis phenotype in women with preterm labor and premature rupture of the membranes.

Authors:  W F O'Brien; G F Leparc; J Holbrook
Journal:  Infect Dis Obstet Gynecol       Date:  1995

10.  The presence of CA19-9 in serum and saliva from Lewis blood-group negative cancer patients.

Authors:  S Yazawa; T Asao; H Izawa; Y Miyamoto; K L Matta
Journal:  Jpn J Cancer Res       Date:  1988-04
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.