Skip to main content
Archives of Disease in Childhood. Fetal and Neonatal Edition logoLink to Archives of Disease in Childhood. Fetal and Neonatal Edition
. 1999 May;80(3):F226–F229. doi: 10.1136/fn.80.3.f226

Correction for erythroid cell contamination in microassay for immunophenotyping of neonatal lymphocytes

E de Vries, S de Bruin-Versteeg, W Comans-Bitter, R de Groot, G Boerma, F Lotgering, J J M van Dongen
PMCID: PMC1720931  PMID: 10212087

Abstract

Immunophenotyping of blood lymphocyte subpopulations in neonates and young infants is hampered by the limited amount of blood that can be collected. Contamination of the flow cytometric "lympho-gate" by normoblasts and analysed erythrocytes, and therefore the underestimation of the relative frequencies of lymphocyte subpopulations, interferes with the precise calculation of absolute counts.
 A microassay was developed by adapting the lysed whole blood technique. Triple immunostaining in a single antibody staining step was used to reduce washing steps and cell loss. Introduction of a triple staining for CD71 (expressed by erythroid precursors), glycophorin A (GpA, expressed by all erythroid cells), and CD45 (expressed by all leucocytes) permitted the relative frequencies of normoblasts (CD71+/GpA+/CD45- population) and unlysed erythrocytes (CD71-/GpA+/CD45- population)to be identified and measured within the "lympho-gate" of neonatal cord blood samples. Particularly high frequencies were found (median: 31%) in cord blood samples from preterm neonates. These erythroid cells disappear rapidly by 1 week of age The relative frequencies of erythroid cells can be used to calculate correct lymphocyte subpopulation values. Using only 0.5-0.8 ml of blood, this micro- assay would also be suitable for rapid prenatal immunodiagnosis of congenital immunodeficiencies.



Full Text

The Full Text of this article is available as a PDF (178.4 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Comans-Bitter W. M., de Groot R., van den Beemd R., Neijens H. J., Hop W. C., Groeneveld K., Hooijkaas H., van Dongen J. J. Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulations. J Pediatr. 1997 Mar;130(3):388–393. doi: 10.1016/s0022-3476(97)70200-2. [DOI] [PubMed] [Google Scholar]
  2. Kutvirt S. G., Lewis S. L., Simon T. L. Lymphocyte phenotypes in infants are altered by separation of blood on density gradients. Br J Biomed Sci. 1993 Dec;50(4):321–328. [PubMed] [Google Scholar]
  3. Loken M. R., Shah V. O., Dattilio K. L., Civin C. I. Flow cytometric analysis of human bone marrow: I. Normal erythroid development. Blood. 1987 Jan;69(1):255–263. [PubMed] [Google Scholar]
  4. Remy N., Oberreit M., Thoenes G., Wahn U. Lymphocyte subsets in whole blood and isolated mononuclear leucocytes of healthy infants and children. Eur J Pediatr. 1991 Feb;150(4):230–233. doi: 10.1007/BF01955518. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood. Fetal and Neonatal Edition are provided here courtesy of BMJ Publishing Group

RESOURCES