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. 2015 Jun 4;26(1):95–101. doi: 10.1111/bpa.12264

Table 2.

Transmission of sCJD MM1+2C, MM1 or MM2C to PrP‐humanized knock‐in mice

Inoculum (ID) Mouse line (human PRNP genotypes at codons 129 and 219)
Ki‐Hu129M/M (M/M, E/E) Ki‐Hu129M/V (M/V, E/E) Ki‐Hu129V/V (V/V, E/E) Ki‐Hu219K/K (M/M, K/K) Ki‐ChM
MM1+2C (case #1) 615 ± 8 (6/6)a ND 717 ± 44 (6/6) 647 ± 49 (5/5) 162 ± 13 (6/6)
MM1+2C (case #2) 580 ± 8 (5/5) 595 ± 6 (4/4) 588 ± 11 (4/4) 594 ± 10 (5/5) 160 ± 9 (4/4)
MM1 (H3)b 467 ± 24 (8/8) 490 ± 26 (5/5) 774 ± 32 (6/6) 573 ± 52 (5/5) 142 ± 3 (5/5)
MM1 (NR) 531 ± 47 (5/5) 508 ± 55 (6/6) 588 ± 3 (5/5) 527 ± 31 (6/6) 154 ± 5 (6/6)
MM2Cc — (0/7) — (0/7) — (0/7) — (0/8) — (0/6)
a

Mean incubation periods (days ± SEM) and attack rates (number of mice positive for PrP accumulation in immunohistochemical analysis/number of inoculated mice).

b

Transmission data of sCJD MM1 prions (H3) have been reported previously 10, 16, 17, 18, 34.

c

None of the sCJD MM2C prion‐inoculated mice had developed disease by the end of their life span. Transmission data of Ki‐Hu129M/M, Ki‐Hu129M/V and Ki‐Hu129V/V have been reported previously 18.

Abbreviation: ND = not done.