Abstract
C3H mice are highly susceptible to the Brazil strain of Trypanosoma cruzi. These mice usually die during the acute phase of infection and develop a profound immunosuppression to heterologous and parasite antigen. In this study, we confirmed earlier reports that infected mice maintained at elevated environmental temperature (36 degrees C) are significantly more resistant to T. cruzi than are mice kept at 20 to 24 degrees C. To determine whether the benefits of increased environmental temperature were due to alterations in the host immune system, the production of antibody to heterologous antigen and the development of parasite-specific T-helper cells were examined in noninfected and T. cruzi-infected mice. Mice were immunized with either sheep erythrocytes (SRBC) or trinitrophenyl groups (TNP) conjugated to fixed culture forms of T. cruzi, and the splenic direct plaque-forming cell (DPFC) responses to SRBC and to TNP-conjugated SRBC were determined. The DPFC response to SRBC from infected mice maintained at elevated environmental temperature was much higher than the suppressed response of infected mice held at room temperature and slightly higher than the response of age-matched noninfected control mice. Likewise, maintaining infected mice at 36 degrees C significantly enhanced the parasite-specific responses of T-helper cells, as reflected by anti-TNP DPFC responses of mice immunized with TNP-conjugated TC.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Amrein Y. U. Effects of environmental temperature on Trypanosoma cruzi infection in mice. J Parasitol. 1967 Dec;53(6):1160–1160. [PubMed] [Google Scholar]
- Burgess D. E., Kuhn R. E., Carlson K. S. Induction of parasite-specific helper T lymphocytes during Trypanosoma cruzi infections in mice. J Immunol. 1981 Nov;127(5):2092–2095. [PubMed] [Google Scholar]
- Choromanski L., Kuhn R. E. Interleukin 2 enhances specific and nonspecific immune responses in experimental Chagas' disease. Infect Immun. 1985 Nov;50(2):354–357. doi: 10.1128/iai.50.2.354-357.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Choromanski L., Kuhn R. E. Repeated antigenic stimulation overcomes immunosuppression in experimental Chagas' disease. Immunology. 1986 Oct;59(2):289–294. [PMC free article] [PubMed] [Google Scholar]
- Cunningham D. S., Kuhn R. E. Trypanosoma cruzi-induced suppression of the primary immune response in murine cell cultures to T-cell-dependent and -independent antigens. J Parasitol. 1980 Feb;66(1):16–27. [PubMed] [Google Scholar]
- Dinarello C. A. Interleukin-1 and the pathogenesis of the acute-phase response. N Engl J Med. 1984 Nov 29;311(22):1413–1418. doi: 10.1056/NEJM198411293112205. [DOI] [PubMed] [Google Scholar]
- Duff G. W., Durum S. K. The pyrogenic and mitogenic actions of interleukin-1 are related. Nature. 1983 Aug 4;304(5925):449–451. doi: 10.1038/304449a0. [DOI] [PubMed] [Google Scholar]
- Gottlieb C. F. Application of transformations to normalize the distribution of plaque-forming cells. J Immunol. 1974 Jul;113(1):51–57. [PubMed] [Google Scholar]
- Jampel H. D., Duff G. W., Gershon R. K., Atkins E., Durum S. K. Fever and immunoregulation. III. Hyperthermia augments the primary in vitro humoral immune response. J Exp Med. 1983 Apr 1;157(4):1229–1238. doi: 10.1084/jem.157.4.1229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jerne N. K., Henry C., Nordin A. A., Fuji H., Koros A. M., Lefkovits I. Plaque forming cells: methodology and theory. Transplant Rev. 1974;18:130–191. doi: 10.1111/j.1600-065x.1974.tb01588.x. [DOI] [PubMed] [Google Scholar]
- Kierszenbaum F., Pienkowski M. M. Thymus-dependent control of host defense mechanisms against Trypanosoma cruzi infection. Infect Immun. 1979 Apr;24(1):117–120. doi: 10.1128/iai.24.1.117-120.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuhn R. E., Murnane J. E. Trypanosoma cruzi: immune destruction of parasitized mouse fibroblasts in vitro. Exp Parasitol. 1977 Feb;41(1):66–73. doi: 10.1016/0014-4894(77)90130-8. [DOI] [PubMed] [Google Scholar]
- Lederman H. M., Brill C. R., Murphy P. A. Interleukin 1-driven secretion of interleukin 2 is highly temperature-dependent. J Immunol. 1987 Jun 1;138(11):3808–3811. [PubMed] [Google Scholar]
- Marinkelle C. J., Rodriguez E. The influence of environmental temperature on the pathogenicity of Trypanosoma cruzi in mice. Exp Parasitol. 1968 Oct;23(2):260–263. doi: 10.1016/0014-4894(68)90067-2. [DOI] [PubMed] [Google Scholar]
- Otieno L. H. Effects of immunosuppressive agents on the course of Trypanosoma (trypanozoon) brucei infections in heat-stressed mice. Trans R Soc Trop Med Hyg. 1973;67(6):856–869. doi: 10.1016/0035-9203(73)90015-1. [DOI] [PubMed] [Google Scholar]
- Otieno L. H. Influence of ambient temperature on the course of experimental trypanosomiasis in mice. Ann Trop Med Parasitol. 1972 Mar;66(1):15–24. doi: 10.1080/00034983.1972.11686793. [DOI] [PubMed] [Google Scholar]
- Powell M. R., Kuhn R. E. Measurement of cytolytic antibody in experimental Chagas' disease using a terminal radiolabelling procedure. J Parasitol. 1980 Jun;66(3):399–406. [PubMed] [Google Scholar]
- Sehgal S., Arora S. K. Effect of temperature on Leishmania mexicana amazonensis induced lesions in hamsters. Indian J Med Res. 1987 Jul;86:25–30. [PubMed] [Google Scholar]
- Tarleton R. L., Kuhn R. E. Measurement of parasite-specific immune responses in vitro: evidence for suppression of the antibody response to Trypanosoma cruzi. Eur J Immunol. 1985 Aug;15(8):845–850. doi: 10.1002/eji.1830150820. [DOI] [PubMed] [Google Scholar]
- Tarleton R. L., Kuhn R. E. Restoration of in vitro immune responses of spleen cells from mice infected with Trypanosoma cruzi by supernatants containing interleukin 2. J Immunol. 1984 Sep;133(3):1570–1575. [PubMed] [Google Scholar]
- Trischmann T., Tanowitz H., Wittner M., Bloom B. Trypanosoma cruzi: role of the immune response in the natural resistance of inbred strains of mice. Exp Parasitol. 1978 Aug;45(2):160–168. doi: 10.1016/0014-4894(78)90055-3. [DOI] [PubMed] [Google Scholar]