Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-24T17:00:12.913Z Has data issue: false hasContentIssue false

Early lymphocytic responses to Heligmosomoides polygyrus infections in mice

Published online by Cambridge University Press:  05 June 2009

S. J. Parker
Affiliation:
Department of Zoology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, Scotland, UK
C. J. Inchley*
Affiliation:
Department of Zoology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, Scotland, UK
*
*Author to whom correspondence should be addressed.

Abstract

Responses to parasite antigens were studied in three strains of mice, BALB/c, CBA and NIH, during the initial phases of a primary infection with the intestinal nematode Heligmosomoides polygyrus. Changes in the rate of in vivo cell division were analysed in mesenteric lymph nodes and spleens during the phases of larval maturation and adult establishment, and related to changes in organ size and cellularity. The nature of the proliferating cell populations was also investigated by flow cytometry, carried out on cell suspensions prepared at the time when larval development was complete. The variation in the ability of the strains of mice to become resistant to a challenge infection was manifest as only slight differences in their initial responses to infection. All three strains showed an increase in 125I-iododeoxyuridine incorporation in their mesenteric lymph nodes and spleen, and an increase in B cell frequency over that of T cells in the draining lymph nodes. Although lymph node weight in NIH mice continued to rise over a 4 week period, the majority of responses measured were short lived, peaking 10 to 14 days after infection. The low responder status of CBA mice was thus reflected in a transient and relatively small enlargement of lymphoid tissues, but their early proliferative responses to antigen were similar in scale to those of responder strains.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Ali, N. M. H. & Behnke, J. M. (1983) Nematospiroides dubius: factors affecting the primary response to SRBC in infected mice. Journal of Helminthology, 57, 343353.CrossRefGoogle ScholarPubMed
Ali, N. M. H. & Behnke, J. M. (1985) Observations on the gross changes in the secondary lymphoid organs of mice infected with Nematospiroides dubius. Journal of Helminthology, 59, 167174.CrossRefGoogle ScholarPubMed
Ali, N. M. H., Behnke, J. M. & Manger, B. R. (1985) The pattern of peripheral blood leucocyte changes in mice infected with Nematospiroides dubius. Journal of Helminthology, 59, 8393.CrossRefGoogle ScholarPubMed
Behnke, J. M., Hannah, J. & Pritchard, D. I. (1983) Nematospiroides dubius in the mouse: evidence that adult worms depress the expression of homologous immunity. Parasite Immunology, 5, 397408.CrossRefGoogle ScholarPubMed
Behnke, J. M. & Robinson, M. (1985) Genetic control of immunity to Nematospiroides dubius: a 9-day anthelmintic abbreviated immunizing regime which separates weak and strong responder strains of mice. Parasite Immunology, 7, 235253.CrossRefGoogle ScholarPubMed
Bryant, V. (1973) The life cycle of Nematospiroides dubius, Baylis, 1926 (Nematoda Heligmosomidae). Journal of Helminthology, 47, 263268.CrossRefGoogle ScholarPubMed
Crandall, R. B., Crandall, C. A. & Franco, J. A. (1974) Heligmosomoides polygyrus (= Nematospiroides dubius): humoral and intestinal immunologic responses to infection in mice. Experimental Parasitology, 35, 275287.CrossRefGoogle ScholarPubMed
Hurley, J. C. & Vadas, M. A. (1983) Eosinophilia and the acquisition of resistance to Nematospiroides dubius in mice sensitized with adult worms. Australian Journal of Experimental Biology and Medical Science, 61, 19.CrossRefGoogle ScholarPubMed
Inchley, C. J. (1987) The contribution of B cell proliferation to spleen enlargement in Babesia microti-infected mice. Immunology, 60, 5761.Google ScholarPubMed
Inchley, C. J., Grieve, E. M. & Preston, P. M. (1987) The proliferative response of mouse lymphoid tissues during infections with Babesia microti or Babesia rodhaini. International Journal for Parasitology, 17, 945950.CrossRefGoogle ScholarPubMed
Jenkins, S. N. & Behnke, J. M. (1977) Impairment of primary expulsion of Trichuris muris in mice with Nematospiroides dubius. Parasitology, 75, 7178.CrossRefGoogle ScholarPubMed
Knopf, P. M., Chapman, C. B., Hicks, J. D., Mandel, T. E. & Mitchell, G. F. (1979) Localization of IgGl-producing cells within a hyperstimulated lymph node of mice infected with an intestinal nematode parasite. Immunology Letters, 1, 137140.CrossRefGoogle Scholar
Liu, S. (1965) Pathology of Nematospiroides dubius 1 Primary infections in C3H and Webster mice. Experimental Pathology, 16, 123135.Google Scholar
Losson, B., Lloyd, S. & Soulsby, E. J. L. (1985) Nematospiroides dubius: modulation of the host immunological responsive. Zeitschrift fur Parasitenkunde, 71, 383393.CrossRefGoogle Scholar
Price, P. & Turner, K. J. (1983) Immunological consequences of intestinal helminth infections in C57B1 mice. The effects on lymphoid tissue and reticuloendothelial function. Australian Journal of Experimental Biology and Medical Science, 61, 371382.CrossRefGoogle Scholar
Price, P. & Turner, K. J. (1986) Immunosuppressive effects of extracts of helminth parasites in C57B1 mice. International Journal for Parasitology, 16, 607615.CrossRefGoogle Scholar
Pritchard, D. I., Ali, N. M. H. & Behnke, J. M. (1984) Analysis of the mechanism of immunodepression following heterologous antigenic stimulation during concurrent infection with Nematospiroides dubius. Immunology, 51, 633642.Google ScholarPubMed
Pritchard, D. I. & Behnke, J. M. (1985) The suppression of homologous immunity by soluble adult antigens of Nematospiroides dubius. Journal of Helminthology, 59, 251256.CrossRefGoogle ScholarPubMed
Pritchard, D. I., Williams, D. J. L., Behnke, J. M. & Lee, T. D. G. (1983) The role of IgG1 hypergammaglobulinaemia in immunity to the gastrointestinal nematode Nematospiroides dubius. The immunological purification, antigen-specificity and in vivo anti-parasite effect of IgG1 from immune serum. Immunology, 49, 353365.Google Scholar
Prowse, S. J., Ey, P. L. & Jenkin, C. R. (1978) Immunity to Nematospiroides dubius: cell and immunoglobulin changes associated with the onset of immunity in mice. Australian Journal of Experimental Biology and Medical Science, 56, 237246.CrossRefGoogle ScholarPubMed
Prowse, S. J., Mitchell, G. F., Ey, P. L. & Jenkin, C. R. (1979) The development of resistance in different inbred strains of mice to infection with Nematospiroides dubius. Parasite Immunology, 1, 277288.CrossRefGoogle ScholarPubMed
Sitepu, P., Dobson, C. & Brindley, P. J. (1985) Immunization and immunosuppression in mice reared for high or low immune responsiveness against Nematospiroides dubius. International Journal for Parasitology, 15, 277281.CrossRefGoogle ScholarPubMed
Sukhdeo, M. V. K., O'grady, R. T. & Hsu, S. C. (1984) The site selected by the larvae of Heligmosomoides polygyrus. Journal of Helminthology, 58, 1923.CrossRefGoogle ScholarPubMed