Table 2.

Early prediction of long-term T-cell reconstitution after HSCT for SCID


Parameter

Control subjects

SCID cohort

P*

Poor reconstitution

Good reconstitution

P
Counts of lymphocytes, per μL       
    Naive CD4+ T cells   1432   341   < .001  86   630   .002 
    Memory CD4+ T cells   303   222   .016  253   185   .711  
    Total CD4+ T cells   1662   789   .001  451   1254   .003 
    Naive CD8+ T cells   603   300   .041  146   323   .153  
    Memory CD8+ T cells   150   75   .246   69   80   .672  
    Total CD8+ T cells   697   552   .412   419   640   .328  
    Total CD19+/CD20+ B cells   677   381   .059   70   649   .005 
    Total CD3-CD16/56+ NK cells   193   127   .014  119   129   .625  
Ki-67 expression, %       
    Total CD4+ T cells   3.0   6.1   .07   6.4   5.8   .25  
    Naive CD4+ T cells   1.1   2.6   .24   3.2   2.0   .27  
TRECs       
    Content in CD4+ T cells, no. per cell   0.20   0.03   .006  0.007   0.11   .005 
    Content in CD8+ T cells, no. per cell   0.10   0.04   .082   0.002   0.10   .013 
    No. in CD4+ T cells/μL blood   410   23   .001  1.4   105   .002 
    No. in CD8+ T cells/μL blood   101   16   .039  0.2   51   .005 
Telomere length, relative to donor       
    Naive CD4+ T cells   ND   NA   NA   1.3   1.6   .079  
    Memory CD4+ T cells   ND   NA   NA   1.1   1.3   .240  
Other parameters       
    Age of patient at HSCT, y   NA   0.7    0.4   0.7   .020 
    Age of donor at HSCT, y   NA   24.2    15.9   27.9   .457  
    SCID phenotype, no.        
        NK-  NA   9    1   8   .007 
        B-  NA   6    5   1   .025 
    B cells predominantly of donor origin, no.   NA   11    4   7   .578  
    NK cells predominantly of donor origin, no.   NA   11    2   9   .023 
    Monocytes predominantly of donor origin, no.   NA   5    0   5   .016 
    Myeloablative conditioning, BU/CY, no.
 
NA
 
11
 

 
4
 
7
 
.578
 

Parameter

Control subjects

SCID cohort

P*

Poor reconstitution

Good reconstitution

P
Counts of lymphocytes, per μL       
    Naive CD4+ T cells   1432   341   < .001  86   630   .002 
    Memory CD4+ T cells   303   222   .016  253   185   .711  
    Total CD4+ T cells   1662   789   .001  451   1254   .003 
    Naive CD8+ T cells   603   300   .041  146   323   .153  
    Memory CD8+ T cells   150   75   .246   69   80   .672  
    Total CD8+ T cells   697   552   .412   419   640   .328  
    Total CD19+/CD20+ B cells   677   381   .059   70   649   .005 
    Total CD3-CD16/56+ NK cells   193   127   .014  119   129   .625  
Ki-67 expression, %       
    Total CD4+ T cells   3.0   6.1   .07   6.4   5.8   .25  
    Naive CD4+ T cells   1.1   2.6   .24   3.2   2.0   .27  
TRECs       
    Content in CD4+ T cells, no. per cell   0.20   0.03   .006  0.007   0.11   .005 
    Content in CD8+ T cells, no. per cell   0.10   0.04   .082   0.002   0.10   .013 
    No. in CD4+ T cells/μL blood   410   23   .001  1.4   105   .002 
    No. in CD8+ T cells/μL blood   101   16   .039  0.2   51   .005 
Telomere length, relative to donor       
    Naive CD4+ T cells   ND   NA   NA   1.3   1.6   .079  
    Memory CD4+ T cells   ND   NA   NA   1.1   1.3   .240  
Other parameters       
    Age of patient at HSCT, y   NA   0.7    0.4   0.7   .020 
    Age of donor at HSCT, y   NA   24.2    15.9   27.9   .457  
    SCID phenotype, no.        
        NK-  NA   9    1   8   .007 
        B-  NA   6    5   1   .025 
    B cells predominantly of donor origin, no.   NA   11    4   7   .578  
    NK cells predominantly of donor origin, no.   NA   11    2   9   .023 
    Monocytes predominantly of donor origin, no.   NA   5    0   5   .016 
    Myeloablative conditioning, BU/CY, no.
 
NA
 
11
 

 
4
 
7
 
.578
 

NK-cell chimerism in the group with poor long-term immune reconstitution was based on 7 patients because hardly any NK cells were present in one of the patients. For the SCID cohort, n = 19; for the group with poor reconstitution, n = 8; for the group with good reconstitution, n = 11.

BU indicates busulphan; CY, cyclophosphamide; ND, not done; NA, not applicable.

*

Median parameters of the whole SCID cohort at early follow-up (1-4 years after HSCT) were compared with age-matched healthy control subjects.

Within the SCID cohort, median parameters of immunity at early follow-up and HSCT-related variables were compared between the groups of patients with poor and good T-cell reconstitution at late follow-up.

Significant differences in P values.

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