Literature DB >> 1901641

Interferon-gamma-mediated effects upon immunity to coccidial infections in the mouse.

M E Rose1, D Wakelin, P Hesketh.   

Abstract

The effect of treatment with a monoclonal antibody (MoAb) capable of neutralising interferon-gamma (IFN-gamma) on the course of coccidial infections in mice (C57BL/6 and NIH infected with Eimeria vermiformis or E. pragensis, and BALB/c infected with E. pragensis) was examined. The results differed with the species of parasite, the strain of mouse, the measure of infection and whether the infection was a primary or secondary one. The replication of E. vermiformis in primary infections was enhanced in both C57BL/6 and NIH mice, but less MoAb was required in NIH than in C57BL/6 to produce similar effects. In neither strain did treatment prevent priming or interfere with the complete immunity to challenge normally induced by moderate infection with E. vermiformis. The replication of E. pragensis in primary infections was not affected in any of the strains of mouse but the clinical effects were exacerbated. Priming with E. pragensis was unaffected by treatment but the partial immunity to challenge, normally induced by infection with this species, was reduced when MoAb was given 2 h before challenge. This reduction was evident as an increased faecal output of oocysts and loss of body weight. These results confirm the role of IFN-gamma in resistance to coccidiosis and further emphasise the complexity of the immune response in this disease.

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Year:  1991        PMID: 1901641     DOI: 10.1111/j.1365-3024.1991.tb00263.x

Source DB:  PubMed          Journal:  Parasite Immunol        ISSN: 0141-9838            Impact factor:   2.280


  17 in total

1.  Apicomplexan parasite, Eimeria falciformis, co-opts host tryptophan catabolism for life cycle progression in mouse.

Authors:  Manuela Schmid; Maik J Lehmann; Richard Lucius; Nishith Gupta
Journal:  J Biol Chem       Date:  2012-04-25       Impact factor: 5.157

2.  Cytotoxic effects of natural killer cells have no significant role in controlling infection with the intracellular protozoon Eimeria vermiformis.

Authors:  M E Rose; P Hesketh; D Wakelin
Journal:  Infect Immun       Date:  1995-09       Impact factor: 3.441

3.  An alphabeta T-cell-independent immunoprotective response towards gut coccidia is supported by gammadelta cells.

Authors:  A L Smith; A C Hayday
Journal:  Immunology       Date:  2000-11       Impact factor: 7.397

4.  Nonspecific immune responses and mechanisms of resistance to Eimeria papillata infections in mice.

Authors:  M L Schito; J R Barta
Journal:  Infect Immun       Date:  1997-08       Impact factor: 3.441

5.  Immune responses to Cryptosporidium muris and Cryptosporidium parvum in adult immunocompetent or immunocompromised (nude and SCID) mice.

Authors:  V McDonald; R Deer; S Uni; M Iseki; G J Bancroft
Journal:  Infect Immun       Date:  1992-08       Impact factor: 3.441

6.  Antigenic diversity in Eimeria maxima and the influence of host genetics and immunization schedule on cross-protective immunity.

Authors:  Adrian L Smith; Patricia Hesketh; Andrew Archer; Martin W Shirley
Journal:  Infect Immun       Date:  2002-05       Impact factor: 3.441

Review 7.  Avian gut-associated lymphoid tissues and intestinal immune responses to Eimeria parasites.

Authors:  H S Lillehoj; J M Trout
Journal:  Clin Microbiol Rev       Date:  1996-07       Impact factor: 26.132

8.  Genetic dissection of primary and secondary responses to a widespread natural pathogen of the gut, Eimeria vermiformis.

Authors:  A L Smith; A C Hayday
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

9.  X-irradiation of Eimeria tenella oocysts provides direct evidence that sporozoite invasion and early schizont development induce a protective immune response(s).

Authors:  M C Jenkins; P C Augustine; H D Danforth; J R Barta
Journal:  Infect Immun       Date:  1991-11       Impact factor: 3.441

10.  The role of natural killer cells in resistance to coccidiosis: investigations in a murine model.

Authors:  A L Smith; M E Rose; D Wakelin
Journal:  Clin Exp Immunol       Date:  1994-08       Impact factor: 4.330

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