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6. IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model. Doolan DL, Hoffman SL. J Immunol; 1999 Jul 15; 163(2):884-92. PubMed ID: 10395683 [Abstract] [Full Text] [Related]
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15. MHC class I-dependent presentation of exoerythrocytic antigens to CD8+ T lymphocytes is required for protective immunity against Plasmodium berghei. White KL, Snyder HL, Krzych U. J Immunol; 1996 May 01; 156(9):3374-81. PubMed ID: 8617963 [Abstract] [Full Text] [Related]
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18. Role of delayed type hypersensitivity responses in protection during chronic Plasmodium berghei infection as evidenced by homing of radiolabelled bone marrow cells and contact sensitivity. Wangoo A, Ganguly NK, Mahajan RC. Jpn J Exp Med; 1990 Apr 15; 60(2):45-50. PubMed ID: 2200902 [Abstract] [Full Text] [Related]
19. A bicistronic DNA vaccine containing apical membrane antigen 1 and merozoite surface protein 4/5 can prime humoral and cellular immune responses and partially protect mice against virulent Plasmodium chabaudi adami DS malaria. Rainczuk A, Scorza T, Spithill TW, Smooker PM. Infect Immun; 2004 Oct 15; 72(10):5565-73. PubMed ID: 15385453 [Abstract] [Full Text] [Related]
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