Table 4.

Detailed Chimerism Analysis in Activated CD4+ and CD8+ T-Cell Subsets One Year After Allo-BMT

Sample T-Cell Population4-150Chimerism4-151
Patient 1 CD4+ HLA-DR R/D 
 CD4+ HLA-DR+ 
 CD8+ HLA-DR R/d 
 CD8+ HLA-DR+ D  
Patient 2 CD4+ HLA-DR 
 CD4+ HLA-DR+ 
 CD8+ HLA-DR 
 CD8+ HLA-DR+ 
Sample T-Cell Population4-150Chimerism4-151
Patient 1 CD4+ HLA-DR R/D 
 CD4+ HLA-DR+ 
 CD8+ HLA-DR R/d 
 CD8+ HLA-DR+ D  
Patient 2 CD4+ HLA-DR 
 CD4+ HLA-DR+ 
 CD8+ HLA-DR 
 CD8+ HLA-DR+ 
F4-150

The T-cell populations were FACS-sorted CD4+ and CD8+ T-cell subsets, cultured for 10 to 14 days in the presence of PHA/rIL-2 and subsequently subjected to a second FACS-sort to generate the DR/DR+,high T-cell fractions, using anti-CD4, anti-CD8, and anti-HLA-DR specific MoAbs.

F4-151

The chimerism patterns were determined via FACS-PCR-CA repeat analysis.38 The predominant origin of the T-cell population is given in capital letters, either donor (D) or recipient (R), whereas a minor population (<10%) is given in lowercase letters (d or r). If donor and recipient were present in equal amounts, both populations were given in capital letters (D/R). The origin of all other hematopoietic cell lineages is depicted in Table 1.

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