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Parameters of intestinal inflammation in mice given graded infections of the nematode Trichinella spiralis

Published online by Cambridge University Press:  12 April 2024

M.S. Dehlawi
Affiliation:
School of Life and Environmental Sciences, University of Nottingham, Nottingham, NG7 2RD, UK
D. Wakelin*
Affiliation:
School of Life and Environmental Sciences, University of Nottingham, Nottingham, NG7 2RD, UK
*
*Author for correspondence Fax: 44 115 9513252 E-mail: [email protected]
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Abstract

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Four parameters of the intestinal inflammatory response (numbers of mucosal mast cells (MMC) and Paneth cells, villus:crypt ratios and mitotic figures) were measured in mice exposed to varying doses of infective larvae of Trichinella spiralis.The aim of the experiments was to determine whether generation of these components of inflammation required a threshold level of infection and whether, once triggered, inflammation became pan-mucosal. Near maximal MMC and Paneth cell responses were elicited even with infections as low as 35 larvae; changes in villus:crypt ratios and in mitotic indices also occurred at this level of infection, but were progressively greater with increasing levels of infection. In all infected mice, including those infected with 35 larvae, MMC and Paneth cell responses extended over most of the small intestine. These data are interpreted as showing: (i) that the intestinal mucosa is highly responsive to T. spiralis infection; (ii) that once triggered, components of the inflammatory response are amplified by T cell-dependent mechanisms, becoming pan-mucosal; and (iii) that MMC and Paneth cell responses, which require cell division and differentiation, become maximal at a lower infection threshold than changes in the villus:crypt ratio or in mitotic indices, which directly reflect increased rates of division in crypt cells.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2002

References

Alizadeh, H. & Wakelin, D. (1982) Genetic factors controlling the intestinal mast cell response in mice infected with Trichinella spiralis . Clinical and Experimental Immunology 49, 331337.Google ScholarPubMed
Dehlawi, M.S. & Wakelin, D. (1995) Dose-dependency of mucosal mast cell responses in mice infected with Trichinella spiralis . Research and Reviews in Parasitology 55, 2124.Google Scholar
Dehlawi, M.S., Wakelin, D. & Behnke, J.M. (1987) Suppression of mucosal mastocytosis by infection with the intestinal nematode Nematospiroides dubius . Parasite Immunology 9, 187194.CrossRefGoogle ScholarPubMed
Despommier, D.D. (1993) Trichinella spiralis and the concept of niche. Journal of Parasitology 79, 472482.CrossRefGoogle ScholarPubMed
Garside, P., Grencis, R.K. & Mowat, A.M. (1992) T lymphocyte dependent enteropathy in murine Trichinella spiralis infection. Parasite Immunology 14, 217225.CrossRefGoogle ScholarPubMed
Garside, P., Kennedy, M.W., Wakelin, D. & Lawrence, C.E. (2000) Immunopathology of intestinal helminth infection. Parasite Immunology 22, 605612.CrossRefGoogle ScholarPubMed
Grencis, R.K. (1997) Th2-mediated host-protective immunity to intestinal nematode infections. Philosophical Transactions of the Royal Society of London B 352, 13771384.CrossRefGoogle ScholarPubMed
Grencis, R.K. & Wakelin, D. (1982) Short-lived dividing cells mediate adoptive transfer of immunity to Trichinella spiralis in mice. I. Availability of cells in primary and secondary infections in relation to cellular changes in the mesenteric lymph node. Immunology 46, 443450.Google ScholarPubMed
Kamal, M., Wakelin, D. & Mahida, Y. (2001a) Mucosal responses to infection with Trichinella spiralis in mice. Parasite 8, S110S113.CrossRefGoogle ScholarPubMed
Kamal, M., Wakelin, D., Oulette, A.J., Smith, A., Podolsky, D.K. & Mahida, Y. (2001b) Mucosal T cells regulate Paneth and intermediate cell numbers in the small intestine of T. spiralis-infected mice. Clinical and Experimental Immunology 126, 117125.CrossRefGoogle ScholarPubMed
Lawrence, C.E., Paterson, J.C., Higgins, L.M., Macdonald, T.T., Kennedy, M.W. & Garside, P. (1998) IL-4-regulated enteropathy in an intestinal nematode infection. European Journal of Immunology 28, 26722684.3.0.CO;2-F>CrossRefGoogle Scholar
Ortega-Pierres, M.G., Yepez-Mulia, L., Homan, W., Gamble, H.R., Lim, P.L., Takahashi, Y., Wassom, D.L. & Appleton, J.A. (1996) Workshop on a detailed characterization of Trichinella spiralis antigens: a platform for future studies on antigens and antibodies to this parasite. Parasite Immunology 18, 273284.CrossRefGoogle ScholarPubMed
Subbuswamy, S.G. (1973) Paneth cells and goblet cells. Journal of Pathology 111, 181189.CrossRefGoogle ScholarPubMed
Wakelin, D. & Lloyd, M. (1976) Immunity to primary and challenge infections of Trichinella spiralis in mice: a re-examination of conventional parameters. Parasitology 72, 173182.CrossRefGoogle ScholarPubMed