Protective immunity against lethal anaphylactic reaction in Toxoplasma gondii -infected mice by DNA vaccination with T. gondii -derived heat shock protein 70 gene
Abstract Toxoplasma gondii -derived heat shock protein 70 ( T.g. HSP70) was proven to induce lethal anaphylactic reaction in T. gondii -infected mice through platelet-activating factor (PAF)-mediated, but not classical IgE-dependent, pathway via TLR4/MyD88 signal pathway. The effector cells generati...
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Published in | Parasitology international Vol. 59; no. 2; pp. 105 - 111 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ireland Ltd
01.06.2010
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract Toxoplasma gondii -derived heat shock protein 70 ( T.g. HSP70) was proven to induce lethal anaphylactic reaction in T. gondii -infected mice through platelet-activating factor (PAF)-mediated, but not classical IgE-dependent, pathway via TLR4/MyD88 signal pathway. The effector cells generating PAF and causing T.g. HSP70-induced anaphylactic reaction were CD11b+ and CD11c+ cells, although the reaction was enhanced by marked IFN-γ production by CD11b+ , CD11c+ , CD4+ and CD8+ splenocytes. In the present study, the effects of T.g. HSP70 gene vaccine targeting peripheral dendritic cells were evaluated against T.g. HSP70-induced anaphylactic reaction in T. gondii -infected mice. C57BL/6 mice receiving T.g. HSP70 gene vaccine showed prolonged survival. Platelets of peripheral blood, which completely disappeared during the T.g. HSP70-induced anaphylactic reaction, were partially restored with the T.g. HSP70 gene vaccination. The T.g. HSP70-induced marked production of PAF and IFN-γ from splenocytes of infected mice during the T.g. HSP70-induced anaphylactic reaction was shown to decrease after the T.g. HSP70 gene vaccination. Thus, T.g. HSP70 gene vaccine induced protective immunity against T.g. HSP70-induced PAF-mediated lethal anaphylactic reaction in T. gondii -infected mice. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1383-5769 1873-0329 |
DOI: | 10.1016/j.parint.2010.03.006 |