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. 2001 May;158(5):1851–1857. doi: 10.1016/s0002-9440(10)64141-7

Table 3.

Single-Cell PCR Analysis in AILD

Case Single CD4+ cells Single CD8+ cells Single Ki67+ cells
Number of specific PCR products/ number of cells Functional/ nonfunctional sequences Clonal*/unique sequences Number of specific PCR products/ number of cells Functional/ nonfunctional sequences Clonal*/unique sequences Number of specific PCR products/ number of cells Functional/ nonfunctional sequences Clonal*/unique sequences
1 9 /32 9 /0 7 /2 12 /32 10 /2 0 /10 3 /32 3 /0 3 /0
2 2 /32 2 /0 2 /0 9 /52 6 /3 0 /7 3 /48 3 /0 3 /0
3 11 /32 9 /2 6 /3 19 /84 13 /6 2 /11 6 /32 6 /0 5 /1
4 16 /48 15 /1 0 /15 12 /32 8 /4 0 /8 19 /48 17 /2 0 /17
5 8 /48 8 /0 5 /3 7 /48 5 /1 0 /5 11 /44 11 /0 7 /4
6 23 /72 20 /3 0 /20 10 /72 8 /1 0 /8 4 /72 4 /0 0 /4
7 11 /54 11 /0 0 /11 13 /36 12 / 0 /12 5 /54 3 / 0 /3
Controls 0 /106 0 /118 0 /110

*In each of the four cases harboring clones, the same clonal rearrangements were detected in the CD4+ and Ki67+ cells. Only potentially functional sequences were considered.

The reading frame of a few sequences could not be unequivocally determined.

Controls include aliquots of the buffer covering the sections during micromanipulation and PCR buffer.