Alterations in the immune phenotype of thymectomized children and the development of atopic disorders after heart transplantation.

Abstract

Atopic disorders are more common in children after heart transplant (HTx). We hypothesized that HTx at an early age and thymus excision (TE) affect development of T and B cells, especially regulatory T cells (Tregs), which help maintain tolerance. In this single-center study including 24 patients transplanted between 2013 and 2018, we investigated lymphocyte patterns in relation to these factors using flow cytometry. Clinical data were collected from standardized questionnaires and medical charts. Patients were stratified into TE and non-TE groups as well as patients with and without post-transplant atopy development/worsening. 64% of TE patients experienced new or worsening asthma/eczema post-transplant compared to 20% of non-TE patients. TE patients had higher total Treg proportions (CD4+CD25+CD127lo) than non-TE patients (p=.043), but borderline significantly lower naïve Tregs (CD45RA+CD27-) (p=.057). Memory CD4+ T cells were higher in TE patients in trend (p=.084). Total Tregs did not differ between atopic/nonatopic groups, although naïve Tregs were significantly lower in atopic patients (p=.028). Memory CD4+ T cells were higher in atopic patients in trend (p=.082). IgM+IgD+ B cells were higher in nonatopic patients in trend (p=.064). New/worsening atopy is more common in thymectomized HTx children and is associated with alterations in T-cell profiles. Avoiding TE may prevent these alterations and reduce incidence of atopy post-HTx.