Table 3

Histopathological and immunohistochemical changes in individual tumor samples induced by eCPMV immunotherapy

PatientKi-67 (%)CC-3 (%)MPO (%)IL-8CD3*CD20*FoxP3*FoxP3/CD3Total necrosis (%)‡NAN (%)nNAN (%)
eCPMV-treated canine IMC patients
P1
 Pretreated0.860.00241.89162.5363.680.260.000.000.00
 Post-treated (day 92)41.4212.0015.452.001422.32944.63133.050.095.385.190.19
P2
 Pretreated37.9317.090.990.00258.21318.63107.250.420.630.000.63
 Post-treated (day 156)29.485.182.092.00343.8980.4277.510.230.970.470.50
P5
 Pretreated60.751.001.140.00253.79130.3299.730.390.590.000.59
 Post-treated (day 17)38.596.419.622.00759.79162.7488.150.122.211.430.78
Control canine IMC patients
P682.248.360.560.00107.16160.3241.470.390.040.040.00
P770.703.292.500.00258.21145.5857.880.220.010.000.01
P848.883.130.261.00326.00307.26142.740.440.000.000.00
  • *The number of CD3-positive, CD20-positive, and FoxP3-positive cells is provided per mm2.

  • †Ki-67 and CC-3 percentages were not calculated for pretreatment biopsy of P1 due to the low availability of neoplastic cells in the pretreatment biopsy.

  • ‡The presence of necrosis (total, neutrophil and non-neutrophil associated) was the only histopathological change assessed in H&E.

  • CC-3, cleaved caspase-3; eCPMV, empty cowpea mosaic virus; IL-8, interleukin-8; IMC, inflammatory mammary cancer; MPO, myeloperoxidase; NAN, neutrophil-associated necrosis; nNAN, non-neutrophil-associated necrosis.