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. 1985 Oct;56(2):203–211.

Genetic control of immunity to Trichinella spiralis in mice: capacity of cells from slow responder mice to transfer immunity in syngeneic and F1 hybrid recipients.

D Wakelin, A M Donachie, R K Grencis
PMCID: PMC1453701  PMID: 4054943

Abstract

Mice of the C57BL/10 (B10) strain are slow responders to infection with T. spiralis in terms of ability to expel worms from the intestine. Compared with rapid-responder NIH mice, infection stimulates a slower and reduced blast cell response in the draining mesenteric lymph node (MLN). Transfer of immune cells from the MLN (MLNC) does not accelerate worm expulsion from naive B10 recipient mice, even though MLNC from this strain effectively transfer immunity to (B10 X NIH) F1 recipients. In common with other B10 background mice C57BL/10 show an infection-dose related suppression of immunity to T. spiralis. Such suppression does not appear to determine the response to MLNC, as adoptive transfer into B10 recipients was not enhanced by reducing the level of challenge infection given, and transfer into F1 recipients was unaffected by simultaneous transfer of lymphocyte populations from donors infected at a level which would induce suppression. A hypothesis is proposed which relates slow response status to (i) the inherent capacity of the intestinal inflammatory component of worm expulsion, and (ii) the outcome of infection-dose related stimulatory and suppressive influences acting on the two interacting lymphocyte components of expulsion. The relevance of H-2-linked and non-H-2 genes to the control of the response is discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bell R. G., Adams L. S., Ogden R. W. Trichinella spiralis: genetics of worm expulsion in inbred and F1 mice infected with different worm doses. Exp Parasitol. 1984 Dec;58(3):345–355. doi: 10.1016/0014-4894(84)90051-1. [DOI] [PubMed] [Google Scholar]
  2. Bell R. G., McGregor D. D., Adams L. S. Trichinella spiralis: genetic basis for differential expression of phase-specific intestinal immunity in inbred mice. Exp Parasitol. 1982 Jun;53(3):315–325. doi: 10.1016/0014-4894(82)90074-1. [DOI] [PubMed] [Google Scholar]
  3. Grencis R. K., Lee T. D., Wakelin D. Adoptive transfer of immunity to Trichinella spiralis in mice: generation of effective cells by different life cycle stages. Int J Parasitol. 1985 Apr;15(2):195–202. doi: 10.1016/0020-7519(85)90087-6. [DOI] [PubMed] [Google Scholar]
  4. Grencis R. K., Riedlinger J., Wakelin D. L3T4-positive T lymphoblasts are responsible for transfer of immunity to Trichinella spiralis in mice. Immunology. 1985 Oct;56(2):213–218. [PMC free article] [PubMed] [Google Scholar]
  5. Grencis R. K., Wakelin D. 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. 1982 Jun;46(2):443–450. [PMC free article] [PubMed] [Google Scholar]
  6. Lee T. D., Wakelin D., Grencis R. K. Cellular mechanisms of immunity to the nematode Trichuris muris. Int J Parasitol. 1983 Aug;13(4):349–353. doi: 10.1016/s0020-7519(83)80039-3. [DOI] [PubMed] [Google Scholar]
  7. Wakelin D., Donachie A. M. Genetic control of immunity to Trichinella spiralis: influence of H-2-linked genes on immunity to the intestinal phase of infection. Immunology. 1983 Feb;48(2):343–350. [PMC free article] [PubMed] [Google Scholar]
  8. Wakelin D., Donachie A. M. Genetic control of immunity to parasites: adoptive transfer of immunity between inbred strains of mice characterized by rapid and slow immune expulsion of Trichinella spiralis. Parasite Immunol. 1980 Winter;2(4):249–260. doi: 10.1111/j.1365-3024.1980.tb00057.x. [DOI] [PubMed] [Google Scholar]
  9. Wakelin D., Grencis R. K., Donachie A. M. Short lived, dividing cells mediate adoptive transfer of immunity to Trichinella spiralis in mice. II. In vivo characteristics of the cells. Immunology. 1982 Jun;46(2):451–457. [PMC free article] [PubMed] [Google Scholar]
  10. Wakelin D., Wilson M. M. T and B cells in the transfer of immunity against Trichinella spiralis in mice. Immunology. 1979 May;37(1):103–109. [PMC free article] [PubMed] [Google Scholar]
  11. Wassom D. L., Brooks B. O., Babish J. G., David C. S. A gene mapping between the S and D regions of the H-2 complex influences resistance to Trichinella spiralis infections of mice. J Immunogenet. 1983 Oct;10(5):371–378. doi: 10.1111/j.1744-313x.1983.tb00349.x. [DOI] [PubMed] [Google Scholar]
  12. Wassom D. L., Wakelin D., Brooks B. O., Krco C. J., David C. S. Genetic control of immunity to Trichinella spiralis infections of mice. Hypothesis to explain the role of H-2 genes in primary and challenge infections. Immunology. 1984 Apr;51(4):625–631. [PMC free article] [PubMed] [Google Scholar]

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