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Effacing of the T cell compartment by cardiac transplantation in infancy

  • Brenda M. Ogle
  • , Lori J. West
  • , David J. Driscoll
  • , Scott E. Strome
  • , Raymund R. Razonable
  • , Carlos V. Paya
  • , Marilia Cascalho
  • , Jeffrey L. Platt

Research output: Contribution to journalArticlepeer-review

Abstract

For cardiac transplantation in infants, T cells are depleted and the thymus is removed. These manipulations should cause profound defects in the T cell compartment. To test this concept, 20 subjects who underwent cardiac transplantation in infancy and healthy age-matched subjects were studied. The number of T cells in the blood was nearly normal in all subjects 1-10 years after surgery. However, newly generated T cells were undetectable in 10 recipients and 10-fold less than controls in 10, suggesting absence of thymic function. TCRβ chain diversity, measured by a novel technique, was ∼100-fold lower than controls. T cell function, deduced from levels of human herpesvirus 7 and response to hepatitis B immunization, were notably impaired. Yet cardiac transplant recipients were generally free of opportunistic infections. Our findings demonstrate a novel approach to measuring lymphocyte diversity and suggest that understanding how these subjects resist infection could yield important insights into immune fitness.

Original languageEnglish (US)
Pages (from-to)1962-1967
Number of pages6
JournalJournal of Immunology
Volume176
Issue number3
DOIs
StatePublished - Feb 1 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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