Abstract |
In the acute phase of Toxoplasma infection, the function of both helper T and B cells was suppressed in primary antibody responses to dinitrophenol (DNP)-conjugated protein antigens. During the course of infection, the suppressive effect on T cells seems to continue longer than that on B cells, since suppression in responses to sheep erythrocytes, a T-dependent antigen, persisted longer than those to DNP-Ficoll, a T-independent antigen. Plastic-adherent cells from the spleens of Toxoplasma-infected and X-irradiated (400 rads) mice had strong suppressor activity in primary anti-sheep erythrocyte antibody responses of normal mouse spleen cells in vitro. These data suggest that the activation of irradiation-resistant and plastic-adherent suppressor cells causes the suppression of both T and B cells in Toxoplasma-infected mice.
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Authors | Y Suzuki, A Kobayashi |
Journal | Infection and immunity
(Infect Immun)
Vol. 40
Issue 1
Pg. 1-7
(Apr 1983)
ISSN: 0019-9567 [Print] United States |
PMID | 6219954
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNP-Ficoll
- Immunoglobulin G
- Isoantibodies
- Ficoll
- Immunoglobulin E
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Topics |
- Animals
- Antibody Formation
(radiation effects)
- B-Lymphocytes
(immunology)
- Cell Adhesion
- Female
- Ficoll
(analogs & derivatives, immunology)
- Hemagglutination Tests
- Immunization, Passive
- Immunoglobulin E
(biosynthesis)
- Immunoglobulin G
(biosynthesis)
- Isoantibodies
(biosynthesis)
- Mice
- Mice, Inbred C57BL
- Phagocytosis
- Rats
- Rats, Inbred Strains
- T-Lymphocytes
(immunology)
- T-Lymphocytes, Regulatory
(enzymology, immunology, radiation effects)
- Toxoplasmosis, Animal
(immunology)
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