期刊论文详细信息
Anais da Academia Brasileira de Ciências
Importance of CD8 T cell-mediated immune response during intracellular parasitic infections and its implications for the development of effective vaccines
Mauricio M. Rodrigues2  Silvia B. Boscardin2  José R. Vasconcelos2  Meire I. Hiyane2  Gerson Salay2  Irene S. Soares1 
[1] ,Universidade Federal de São Paulo Escola Paulista de Medicina Departamento de Microbiologia, Imunologia e ParasitologiaSão Paulo SP ,Brasil
关键词: CD8;    parasites;    immunity;    vaccine;    CD8;    parasitas;    imunidade;    vacinas;   
DOI  :  10.1590/S0001-37652003000400005
来源: SciELO
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【 摘 要 】

Obligatory intracellular parasites such as Plasmodium sp, Trypanosoma cruzi, Toxoplasma gondii and Leishmania sp are responsible for the infection of hundreds of millions of individuals every year. These parasites can deliver antigens to the host cell cytoplasm that are presented through MHC class I molecules to protective CD8 T cells. The in vivo priming conditions of specific CD8 T cells during natural infection are largely unknown and remain as an area that has been poorly explored. The antiparasitic mechanisms mediated by CD8 T cells include both interferon-g-dependent and -independent pathways. The fact that CD8 T cells are potent inhibitors of parasitic development prompted many investigators to explore whether induction of these T cells can be a feasible strategy for the development of effective subunit vaccines against these parasitic diseases. Studies performed on experimental models supported the hypothesis that CD8 T cells induced by recombinant viral vectors or DNA vaccines could serve as the basis for human vaccination. Regimens of immunization consisting of two different vectors (heterologous prime-boost) are much more efficient in terms of expansion of protective CD8 T lymphocytes than immunization with a single vector. The results obtained using experimental models have led to clinical vaccination trials that are currently underway.

【 授权许可】

CC BY   
 All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License

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