Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation

Blood. 2001 Feb 15;97(4):880-5. doi: 10.1182/blood.v97.4.880.

Abstract

Human Nude/SCID (severe combined immunodeficiency) is the first severe combined immunodeficiency caused by mutation of the winged-helix-nude (WHN) gene, which is expressed in the thymus but not in the hematopoietic lineage. The disease is characterized by a T-cell defect, congenital alopecia, and nail dystrophy. A Nude/SCID patient who underwent bone marrow transplantation from the human leukocyte antigen-identical heterozygote brother was studied to investigate, in this unique model, the role of the thymus in immunologic reconstitution. Despite an increase in CD3(+), CD4(+), and CD8(+) cells, CD4(+) CD45 RA naive lymphocytes were not regenerated. Conversely, naive CD8(+) cells were normal. After an initial recovery, lymphocyte proliferation to mitogens progressively declined compared with controls and genotypically identical donor cells grown in the WHN(+/-) environment. Analysis of the T-cell receptor (TCR) repertoire of CD4(+) cells revealed that only 3 of 18 Vbeta families had an altered CDR3 heterogeneity length profile. Conversely, CD8(+) lymphocytes showed an abnormal distribution in most Vbeta families. These data indicate that the thymus is differentially required in the reconstitution of CD4(+) and CD8(+) naive subsets and in the maintenance of their TCR repertoire complexity. Taken together, these findings suggest that bone marrow transplantation is ineffective in the long-term cure of this form of SCID.

Publication types

  • Case Reports
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alopecia / congenital
  • Alopecia / genetics*
  • Animals
  • Antibody Formation
  • Consanguinity
  • DNA-Binding Proteins / deficiency*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology
  • Disease Models, Animal
  • Female
  • Follow-Up Studies
  • Forkhead Transcription Factors
  • Gene Rearrangement, T-Lymphocyte
  • Humans
  • Immunophenotyping
  • Infant, Newborn
  • Lymphocyte Activation
  • Male
  • Mice
  • Mice, Nude
  • Mice, SCID
  • Organ Specificity
  • Phenotype
  • Severe Combined Immunodeficiency / classification
  • Severe Combined Immunodeficiency / genetics*
  • Severe Combined Immunodeficiency / pathology
  • Severe Combined Immunodeficiency / therapy
  • Species Specificity
  • T-Lymphocytes / immunology
  • T-Lymphocytes / transplantation
  • Thymus Gland / abnormalities
  • Transcription Factors / deficiency*
  • Transcription Factors / genetics
  • Transcription Factors / physiology
  • Transplantation, Homologous

Substances

  • DNA-Binding Proteins
  • Forkhead Transcription Factors
  • Transcription Factors
  • Whn protein

Grants and funding