Apparent irrelevance of NK cells to resolution of infections with Babesia microti and Plasmodium vinckei petteri in mice
- 1 September 1982
- journal article
- research article
- Published by Wiley in Parasite Immunology
- Vol. 4 (5) , 319-327
- https://doi.org/10.1111/j.1365-3024.1982.tb00443.x
Abstract
Increased natural killer (NK) cell activity was found in the spleen and peritoneal cavity of mice infected with Babesia microti or Plasmodium vinckei petteri. This increased activity appeared not to be associated with the effectiveness of the host response against these parasites, since it reached its maximum when the parasitaemia was still low, and had decreased by the time the parasites reached peak densities. In addition mice pretreated with 89Strontium or 17β-oestradiol experienced the same pattern of infection as did control mice, yet the infections induced much lower levels of NK activity in the pretreated mice. The course of infection with B. microti was also unaltered in beige mice, which are genetically deficient in NK cells. Thus we consider it unlikely that NK cells are of primary importance in non-specific immunity to these haemoprotozoan infections.Keywords
This publication has 15 references indexed in Scilit:
- Hybrid resistance to EL-4 lymphoma cells. I. Characterization of natural killer cells that lyse EL-4 cells and their distinction from marrow-dependent natural killer cells.The Journal of Experimental Medicine, 1979
- A functional comparison of tumor cell killing by activated macrophages and natural killer cellsEuropean Journal of Immunology, 1979
- The beige mutation in the mouse selectively impairs natural killer cell functionNature, 1979
- Current status of the immunology of blood and tissue protozoaExperimental Parasitology, 1977
- Protection of mice againstBabesiaspp. andplasmodiumspp. with killedCorynebacterium parvumParasitology, 1977
- Protection of mice against Babesia, and Plasmodium with BCGNature, 1976
- Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cellsInternational Journal of Cancer, 1975