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Assessment of thymic output in common variable immunodeficiency patients by evaluation of T cell receptor excision circles

Authors :
Vanessa Guazzi
Marina Pierdominici
Ivano Mezzaroma
Fernando Aiuti
R. Fantini
Francesca Mazzetta
Grazia Andolfi
Alessandro Aiuti
Alessandra Mortellaro
Marco Marziali
Guazzi, V
Aiuti, F
Mezzaroma, I
Mazzetta, F
Andolfi, G
Mortellaro, A
Pierdominici, M
Fantini, R
Marziali, M
Aiuti, Alessandro
Source :
Clinical and Experimental Immunology. 129:346-353
Publication Year :
2002
Publisher :
Oxford University Press (OUP), 2002.

Abstract

SUMMARYCommon variable immunodeficiency (CVID) is a heterogeneous syndrome characterized by repeated infections and hypogammaglobulinaemia. Additionally, T-cell abnormalities including lymphopenia, decreased proliferation to mitogens and antigens, and the reduced production and expression of cytokines, have also been observed. In this study we have investigated the expression of naive, memory and activation markers in T-cell subpopulations in 17 CVID patients in comparison to age-matched normal controls. The numbers of CD4+ T cells, including CD45RA+CD62L+ and, to a lesser extent, CD45RA–CD62L+/RA+CD62L– were significantly reduced in patients, whereas CD8+ T cells were within normal range. In contrast, HLA-DR+ cells were increased both in CD4+ and CD8+ T cells. To assess the thymic output, we analysed the presence of T-cell receptor excision circles (TRECs) in CD4+ and CD8+ T cells by quantitative PCR. TRECs were decreased significantly in patients and the rate of TREC loss was higher with increasing age. TRECs correlated with naive CD4+ T cells, whereas there was an inverse relationship between TRECs and CD8+HLA–DR+ and CD8+CD45RA–CD62L+/RA+CD62L– T cells. Our results suggest the presence of a defect in the naive T cell compartment with origin at the thymic level in CVID, and indicate that TREC may be a useful marker to monitor thymic function in this primary immunodeficiency.

Details

ISSN :
13652249 and 00099104
Volume :
129
Database :
OpenAIRE
Journal :
Clinical and Experimental Immunology
Accession number :
edsair.doi.dedup.....b0e85ae0093a4d31ee0ff78f06d84fc9
Full Text :
https://doi.org/10.1046/j.1365-2249.2002.01893.x