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Table 5 NCCR analysis in samples collected from Crohn’s Disease and Multiple Sclerosis patients

From: Human Polyomavirus JC monitoring and noncoding control region analysis in dynamic cohorts of individuals affected by immune-mediated diseases under treatment with biologics: an observational study

A. Crohn’s Disease patients

Samples

N° JCPyV positive samples

N° archetype* (%) (IIS)†

37 T→G and 217 G→A** (IIS) †

N° rearranged NCCR sequences (%)

37 T→G , 217 G→A** and boxD deletion (IIR) †

Mad1-like sequence (IR) †

Urine

34

34 (100%)

0

0

0

Plasma

28

20 (71%)

8 (29%)

0

0

Ileum

21

10 (47%)

7 (33%)

4 (20%)

0

Colon-rectum

16

8 (50%)

5 (32%)

1 (6%)

2 (12%)

Total (%)

99

72 (72%)

20 (21%)

5 (5%)

2 (2%)

B. Multiple Sclerosis patients

Samples

N° JCPyV positive samples

N° archetype* (%) (IIS) †

N° rearranged NCCR sequences (%)

duplication of a 98bp unit and 66bp insert (boxD)(IIR) †

Urine

13

13 (100%)

0

Plasma

7

7 (100%)

0

PBMC

3

1 (33%)

2 (67%)

Total (%)

23

21 (91%)

2 (9%)

  1. * JCPyV archetype CY[38] with random occurrence of few point mutations and constant G to A transition at position nucleotide number 217 in the boxF.
  2. ** T to G transversion at position nucleotide number 37 in the box A within Spi-B binding site, and G to A transition at position nucleotide number 217 in the boxF considering the nucleotide numbering based on non-pathogenic JCPyV archetype CY[38].
  3. † Jensen and Major (2001) NCCR forms classification is also reported[35].