The T-cell receptor (TCR) V? gene usage of CD4 and CD8 T-cell subpopulations was evaluated by flow cytometric analysis and by CDR3 spectratyping in healthy subjects belonging to Sardinian population, which is ethnically homogeneous and genetically distant from all other Italian and Caucasoid groups. As described in healthy Caucasian subjects, we found a nonrandom V? gene usage and in some V? families a significant skewed reactivity toward CD4 T cells. Moreover, different subjects showed expansions in some V? subfamilies, mainly in the CD8 T cells. By CDR3 spectratyping analysis we found a significantly higher degree of skewness in the TCR V? repertoire of CD8 than in that of CD4 T cells. The similarity found in the TCR V? gene usage between the population examined and other Caucasoid groups suggest that the shape of the TCR repertoire is more influenced by rearrangement processes than ethnic background. However, genetic polymorphisms may condition the expression levels of some V?s, determining the variability of the TCR repertoire between different populations. Finally, the profound perturbations evidenced in the CD8 T cell subpopulation could be related to a different response to the antigenic stimulation between CD8 and CD4 T lymphocytes. Human Immunology 64, 689-695 (2003). © American Society for Histocompatibility and Immunogenetics, 2003. Published by Elsevier Inc.
T-cell receptor repertoire in healthy Sardinian subjects
Doro MG;
2003
Abstract
The T-cell receptor (TCR) V? gene usage of CD4 and CD8 T-cell subpopulations was evaluated by flow cytometric analysis and by CDR3 spectratyping in healthy subjects belonging to Sardinian population, which is ethnically homogeneous and genetically distant from all other Italian and Caucasoid groups. As described in healthy Caucasian subjects, we found a nonrandom V? gene usage and in some V? families a significant skewed reactivity toward CD4 T cells. Moreover, different subjects showed expansions in some V? subfamilies, mainly in the CD8 T cells. By CDR3 spectratyping analysis we found a significantly higher degree of skewness in the TCR V? repertoire of CD8 than in that of CD4 T cells. The similarity found in the TCR V? gene usage between the population examined and other Caucasoid groups suggest that the shape of the TCR repertoire is more influenced by rearrangement processes than ethnic background. However, genetic polymorphisms may condition the expression levels of some V?s, determining the variability of the TCR repertoire between different populations. Finally, the profound perturbations evidenced in the CD8 T cell subpopulation could be related to a different response to the antigenic stimulation between CD8 and CD4 T lymphocytes. Human Immunology 64, 689-695 (2003). © American Society for Histocompatibility and Immunogenetics, 2003. Published by Elsevier Inc.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.