Table 3.

Molecular studies and immunohistochemistry in cutaneous samples from patients 1, 2, and 3



Molecular studies

Immunohistochemistry
Epidermis, no. positive cells/mm
Dermis, ratio category
Patient
Immunoscopy: Vβ family of T-cell clones
CD158k*
CD158e
CD3
CD4
CD8
CD158k
CD4/CD3
CD8/CD3
CD158k/CD3
1   17, 6, 16   +   -   68   59   2   2   4   1   1  
1§  17, 15, 16   +   -   54   44   12   9   4   2   2  
2   2   +   -   6   3   0   3   4   0   2  
3
 
8
 
+
 
-
 
32
 
30
 
0
 
14
 
4
 
0
 
3
 


Molecular studies

Immunohistochemistry
Epidermis, no. positive cells/mm
Dermis, ratio category
Patient
Immunoscopy: Vβ family of T-cell clones
CD158k*
CD158e
CD3
CD4
CD8
CD158k
CD4/CD3
CD8/CD3
CD158k/CD3
1   17, 6, 16   +   -   68   59   2   2   4   1   1  
1§  17, 15, 16   +   -   54   44   12   9   4   2   2  
2   2   +   -   6   3   0   3   4   0   2  
3
 
8
 
+
 
-
 
32
 
30
 
0
 
14
 
4
 
0
 
3
 

With the use of immunohistochemistry, the proportion of labeled cells was evaluated separately in the epidermis and in the dermis. In the epidermis, the numbers of CD3+, CD4+, CD8+, and AZ158+ lymphocytes per millimeter were evaluated on the total epidermal length. In the dermis, semiquantitative analysis was performed in which CD4/CD3, CD8/CD3, and AZ158/CD3 ratios were categorized into 4 groups: group 1 (0%-25%), group 2 (greater than 25%-50%), group 3 (greater than 50%-75%), and group 4 (greater 75%-100%).

*

Molecular study of CD158k in the skin consisted of RT-PCR with consensus primers applied to total RNA extracted from the skin samples used for immunohistochemistry.

Molecular study of CD158e in the skin consisted of RT-PCR with consensus primers applied to total RNA extracted from the skin samples used for immunohistochemistry.

Immunohistochemistry analysis for the CD158k+ population was performed using the AZ158 mAb, which recognizes KIR3DL1/CD158e and KIR3DL2/CD158k.

§

Data after 1 year of disease progression.

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