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Publication : Enhancement of dendritic cell activation via CD40 ligand-expressing γδ T cells is responsible for protective immunity to Plasmodium parasites.

First Author  Inoue S Year  2012
Journal  Proc Natl Acad Sci U S A Volume  109
Issue  30 Pages  12129-34
PubMed ID  22778420 Mgi Jnum  J:186477
Mgi Id  MGI:5432422 Doi  10.1073/pnas.1204480109
Citation  Inoue S, et al. (2012) Enhancement of dendritic cell activation via CD40 ligand-expressing gammadelta T cells is responsible for protective immunity to Plasmodium parasites. Proc Natl Acad Sci U S A 109(30):12129-34
abstractText  Previous reports have shown that gammadelta T cells are important for the elimination of malaria parasites in humans and mice. However, how gammadelta T cells are involved in protective immunity against blood-stage malaria remains unknown. We infected gammadelta T-cell-deficient (TCRdelta-KO) mice and control wild-type mice with Plasmodium berghei XAT, which is a nonlethal strain. Although infected red blood cells were eliminated within 30 d after infection, TCRdelta-KO mice could not clear the infected red blood cells, showed high parasitemia, and eventually died. Therefore, gammadelta T cells are essential for clearance of the parasites. Here, we found that gammadelta T cells play a key role in dendritic cell activation after Plasmodium infection. On day 5 postinfection, gammadelta T cells produced IFN-gamma and expressed CD40 ligand during dendritic cell activation. These results suggest that gammadelta T cells enhance dendritic cell activation via IFN-gamma and CD40 ligand-CD40 signaling. This hypothesis is supported strongly by the fact that in vivo induction of CD40 signaling prevented the death of TCRdelta-KO mice after infection with P. berghei XAT. This study improves our understanding of protective immunity against malaria and provides insights into gammadelta T-cell-mediated protective immunity against various infectious diseases.
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