Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A method to detect McLeod phenotype red blood cells.

R Øyen1, M E Reid, P Rubinstein

  • 1Immunohematology Laboratory, New York Blood Center, 310 East 67th Street, New York, NY 10021, USA.

Immunohematology
|January 1, 1996
PubMed
Summary

Identifying the McLeod phenotype is crucial for distinguishing McLeod syndrome from other acanthocytosis causes. Flow cytometry with anti-K14 antibodies effectively identifies McLeod carrier females by detecting distinct red blood cell populations.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Epithelial miR-149-5p up-regulation is associated with immune evasion in progressive bronchial premalignant lesions.

bioRxiv : the preprint server for biology·2025
Same author

Diagnostic accuracy of spot and timed measurements of urinary albumin concentration to determine microalbuminuria in sickle cell disease.

The West Indian medical journal·2014
Same author

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

Vox sanguinis·2013
Same author

The production, serologic evaluation, and epitope mapping of ten murine monoclonal Dombrock antibodies.

Immunohematology·2013
Same author

The molecular basis of the LU:7 and LU:-7 phenotypes.

Immunohematology·2013
Same author

Molecular background of RH in Bastiaan, the RH:-31,-34 index case, and two novel RHD alleles.

Immunohematology·2013

Area of Science:

  • Immunology
  • Hematology
  • Genetics

Background:

  • The McLeod phenotype requires identification to differentiate McLeod syndrome from other acanthocytosis causes like chorea acanthocytosis.
  • Males with McLeod phenotype may have X-linked chronic granulomatous disease.
  • Detecting the McLeod phenotype typically relies on weakened Kell antigens on red blood cells (RBCs) due to limited availability of anti-Kx + -Km antibodies.

Purpose of the Study:

  • To investigate reliable methods for identifying the McLeod phenotype, particularly in carrier females.
  • To evaluate the efficacy of Kell system antibodies, including monoclonal anti-K14, in detecting weakened Kell antigen expression on RBCs.
  • To differentiate McLeod syndrome from other acanthocytosis conditions.

Main Methods:

Related Experiment Videos

  • Testing of RBCs from 12 mother/son or father/daughter pairs using standard hemagglutination tube tests and flow cytometry.
  • Utilized both monoclonal and polyclonal Kell system antibodies, with a focus on monoclonal anti-K14 (G10).
  • Compared agglutination reactions and median fluorescence intensity between McLeod individuals and controls.
  • Main Results:

    • Monoclonal anti-K14 showed weak reactions (+/-) by hemagglutination and low median fluorescence (6-11) with McLeod males' RBCs compared to controls (441).
    • Other Kell antibodies (anti-k) were not suitable for differentiating McLeod phenotype RBCs.
    • Flow cytometry using anti-K14 clearly identified two distinct RBC populations in McLeod carrier females (median fluorescence 6-11 and 229-382).

    Conclusions:

    • Flow cytometry using monoclonal anti-K14 is a highly effective method for identifying McLeod carrier females.
    • Kell system antibodies vary in their ability to detect weakened antigen expression; pre-selected reagents are crucial.
    • This method aids in distinguishing McLeod syndrome from other forms of acanthocytosis.