Abstract
HUMAN papillomaviruses associated with cutaneous1 and ano-genital2 cancers induce intraepithelial precursor lesions which may regress spontaneously or progress into invasive carcinomas3,4. Cell-mediated immune responses are probably involved in regression of precancerous lesions1,5–8 and the polymorphism of the genes responsible may thus have a key role in the variability of the host response. Skin warts and cancers induced in rabbits by Shope papillomavirus9–12 provide a model to test this hypothesis. We analysed a restriction-fragment-length polymorphism of major histocompatibility complex class I and class II genes13,14 and T-cell receptor β-chain genes15 in infected domestic rabbits. We found a strong linkage between wart regression and a DRαEcoRI fragment, and an increased relative risk of malignant transformation associated with a DQα PvuII fragment. This indicates a genetic control of wart evolution, involving genes in the class II region of the major histocompatibility complex.
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Man, R., Breitburd, F., Marche, P. et al. Linkage of regression and malignant conversion of rabbit viral papillomas to MHC class II genes. Nature 356, 66–68 (1992). https://doi.org/10.1038/356066a0
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DOI: https://doi.org/10.1038/356066a0
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