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. 2014 Nov 4;2:116. doi: 10.3389/fped.2014.00116

Table 1.

Immunopathological changes in rodents investigated as models for rheumatic heart disease.

Antigen (route of inoculation) Histological changes Antibody response T cell response cytokine production Cross-reactivity References
RATS (Rattus norvegicus)
Whole GAS (FP, SC) Myocarditis, valvulitis lymphocyte, monocyte, MØ, giant cell, Aschoff-like cell, fibroblast Anti-myocardial IgG NA Valvular protein, myocardial protein Cavelti (3), Huang et al (4), Xie et al (5)
Recombinant proteins or peptides of GAS (SC, IP, FP) Myocarditis, valvulitis T cell, MNC, neutrophil, Anitschkow-like cell Anti-GAS IgG CD3+, CD4+, CD8+, CD68+, TCR-αβ+ Cardiac myosin Quinn et al (6), Lymbury et al (7), Gorton et al (8), Gorton et al (9), Kirvan et al (10)
MICE (Mus musculus)
Cell wall fragments of GAS (IP) Myocarditis MNC, PMNC, giant cell, Anitschkow-like cell Anti-GAS IgG NA NA Ohanian et al (11)
Recombinant protein of GAS (IP) NA Collagen IV reactive IgG NA Basement membrane collagen Dinkla et al (12)
GUINEA PIG (Cavia porcellus)
Whole GAS (IP, IV) Myocarditis, valvulitis MNC NA NA NA Gross et al (13)
Cell wall fragments of GAS (FP) NA Anti-GAS IgG NA Cardiac sarcolemmal membrane Yang et al (14)

NA, not assessed; IV, intra-venous; SC, sub-cutaneous; IP, intra-peritoneal; FP, foot pad; MNC, mononuclear cell; PMNC, polymorphonuclear cell; MØ, macrophage; Ig, immunoglobulin; CD, cluster of differentiation; IFN, interferon; TCR, T cell receptor.