| Literature DB >> 21807053 |
Satish Mishra1, Urvashi Rai, Takayuki Shiratsuchi, Xiangming Li, Yannick Vanloubbeeck, Joe Cohen, Ruth S Nussenzweig, Elizabeth A Winzeler, Moriya Tsuji, Victor Nussenzweig.
Abstract
Immunization of BALB/c mice with irradiated sporozoites (IrSp) of Plasmodium yoelii can lead to sterile immunity. The circumsporozoite protein (CSP) plays a dominant role in protection. Nevertheless after hyper-immunization with IrSp, complete protection is obtained in CSP-transgenic BALB/c mice that are T-cell tolerant to the CSP and cannot produce antibodies [CSP-Tg/JhT(-/-)]. This protection is mediated exclusively by CD8(+) T cells [1]. To identify the non-CSP protective T cell antigens, we studied the properties of 34 P. yoelii sporozoite antigens that are predicted to be secreted and to contain strong Kd-restricted CD8(+) T cell epitopes. The synthetic peptides corresponding to the epitopes were used to screen for the presence of peptide-specific CD8(+) T cells secreting interferon-γ (IFN-γ) in splenocytes from CSP-Tg/JhT(-/-) BALB/c mice hyper immunized with IrSp. However, the numbers of IFN-γ-secreting splenocytes specific for the non-CSP antigen-derived peptides were 20-100 times lower than those specific for the CSP-specific peptide. When mice were immunized with recombinant adenoviruses expressing selected non-CSP antigens, the animals were not protected against challenge with P. yoelii sporozoites although large numbers of CD8(+) specific T cells were generated.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21807053 PMCID: PMC3603353 DOI: 10.1016/j.vaccine.2011.07.081
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641