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Models of superinfection and acquired immunity to multiple parasite strains

Published online by Cambridge University Press:  14 July 2016

P. J. M. Milligan*
Affiliation:
University of Liverpool
D. Y. Downham*
Affiliation:
University of Liverpool
*
Postal address: Medical Research Council Laboratories, Fajara, PO Box 273, Banjul, The Gambia.
∗∗Postal address: Department of Statistics and Computational Mathematics, University of Liverpool, Liverpool L69 3BX, UK.

Abstract

Individuals in communities in which different strains of pathogen are circulating can acquire resistance by accumulating immunity to each strain. After considering susceptibility, models of infection and immunity are defined for vector-borne diseases such as malaria and trypanosomiasis. For these models the prevalence of infection, the number of infections per individual, and the mean duration of infection, increase rapidly in young individuals, but decrease in older individuals as immunity is acquired to the various strains of pathogen; the mean interval between successive infections lengthens with age. The bivariate Poisson distribution is shown to be a close approximation to some stochastic processes. The models explain observed cross-sectional patterns of age prevalence, and longitudinal patterns in which individuals typically continue to become infected as they age, albeit with decreasing frequency. In these models the time spent infected depends on parasite diversity, as well as the inoculation and recovery rates. It is shown that control measures can cause an increase in the number of infections and the prevalence of infection in older individuals, and in the average prevalence in the community, even when strain-specific immunity is life-long.

Type
Research Papers
Copyright
Copyright © Applied Probability Trust 1996 

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References

Aron, J. L. (1983) The dynamics of immunity boosted by exposure to infection. Math. Biosci. 64, 249–59.Google Scholar
Aron, J. L. and May, R. M. (1982) The population dynamics of malaria. In Population Dynamics of Infectious Diseases. ed. Anderson, R. M. Chapman and Hall, London. pp. 139179.CrossRefGoogle Scholar
Bailey, N. T. J. (1982) The Biomathematics of Malaria. Griffin, London.Google Scholar
Cornille-Brogger, R., Matthews, H. M., Storey, J., Ashkar, T. S., Brogger, S. and Molineaux, L. (1978) Changing patterns in the humoral imune response to malaria before, during and after the application of control measures: a longitudinal study in the West African savanna. Bull. World Health Org. 56, 479600.Google Scholar
Dietz, K. (1980) Models of vector-borne parasitic diseases. Lecture Notes Biomath. 39, 264277.Google Scholar
Dietz, K. (1988) Mathematical models for transmission and control of malaria. In Malaria: Principles and Practice of Malariology. ed. Wernsdorfer, W. H. and McGregor, I. Sir. Churchill Livingstone, London. pp. 10911133.Google Scholar
Dietz, K., Molineaux, L. and Thomas, A. (1974) A malaria model tested in the African Savanna. Bull. World Health Org. 50, 347357.Google Scholar
Dwinger, R., Luckins, A. G. Murray, M., Rae, P. and Moloo, S. K. (1985) Interference between different serodemes of Trypanosoma congolense in the establishment of superinfections in goats following tsetse transmission. In ISTCRC 18th meeting, Harare, Zimbabwe, 1985. OAU/STRC, Nairobi. pp. 9699.Google Scholar
Fiennes, R. N. T.-W. (1953) The cattle trypanosomiases – experiments on the maintenance of cattle in tsetse-infested country by means of drug prophylaxis. Brit. Vet. J. 109, 473.Google Scholar
Gupta, S., Trenholme, K., Anderson, R. M. and Day, K. P. (1994a) Antigenic diversity and the transmission dynamics of Plasmodium falciparum. Science 264, 961963.Google Scholar
Gupta, A., Swinton, J. and Anderson, R. M. (1994b) Theoretical studies of the effects of heterogeneity in the parasite population on the transmission dynamics of malaria. Proc. R. Soc. Lond. B 256, 231238.Google Scholar
Macdonald, G. (1950) The analysis of infection rates in diseases in which superinfection occurs. Trop. Diseases Bull. 47, 907915.Google ScholarPubMed
Masake, R. A., Nyambati, V. M., Nantulya, V. M., Majiwa, P. A. O., Moloo, S. K. and Musoke, A. J. (1988) The chromosome profiles of Trypanosoma congolense isolates from Kilifi, Kenya and their relationship to serodeme identity. Mol. Biochem. Parasit. 30, 105112.Google Scholar
Morrison, W. I. Murray, M. and Akol, G. W. O. (1985) Immune responses of cattle to African trypanosomes. In Immunology and Pathogenesis of Trypanosomiasis. ed. Tizard, J. CRC Press, Boca-Raton, FL. pp. 103131.Google Scholar
Nasell, I. (1986) On superinfection in malaria. IMA J. Math. Appl. Med. Biol. 3, 211227.Google Scholar
Regier, C. and Trape, J.-F. (1993) Malaria attacks in children exposed to high transmission: who is protected? Trans. R. Soc. Trop. Medicine Hygiene 87, 245246.Google Scholar
Ross, R. (1916) An application of the theory of probabilities to the study of a priori pathometry, I. Proc. R. Soc. A 92, 204230.Google Scholar
Trail, J. C. M., D'Ieteren, G. D. M., Colardelle, C., Maille, J. C., Ordner, G., Sauveroche, B. and Yangari, G. (1991) Evaluation of a field test for trypanotolerance in young N'Dama cattle. Acta Tropica 48, 4757.Google Scholar
Troye-Blomberg, M. and Perlmann, P. (1994) Malaria immunity: an overview with emphasis on T-cell function. In Molecular Immunological Considerations in Malaria Vaccine Development. ed. Good, M. F. and Saul, A. J. CRC Press, Boca Raton, FL. pp. 146.Google Scholar
Whiteside, E. F. (1962) Interactions between drugs, trypanosomes and cattle in the field. In Drugs, Parasites and Hosts. ed. Goodwin, L. G. and Nimmo-Smith, R. H. Churchill, London. p. 116.Google Scholar