Search Results - (Author, Cooperation:J. Langhorne)
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1P. Wongpan, K. M. Meiners, P. J. Langhorne, P. Heil, I. J. Smith, G. H. Leonard, R. A. Massom, L. A. Clementson, T. G. Haskell
Wiley-Blackwell
Published 2018Staff ViewPublication Date: 2018-02-24Publisher: Wiley-BlackwellPrint ISSN: 0148-0227Topics: GeosciencesPhysicsPublished by: -
2P. J. Spence ; W. Jarra ; P. Levy ; A. J. Reid ; L. Chappell ; T. Brugat ; M. Sanders ; M. Berriman ; J. Langhorne
Nature Publishing Group (NPG)
Published 2013Staff ViewPublication Date: 2013-05-31Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Culicidae/*parasitology ; Erythrocytes/parasitology ; Host-Parasite Interactions/*immunology ; Insect Vectors/*parasitology ; Malaria/immunology/parasitology/transmission ; Malaria Vaccines/immunology ; Mice ; Mice, Inbred C57BL ; Plasmodium chabaudi/growth & development/*immunology/isolation & ; purification/*pathogenicity ; Serial Passage ; Virulence/immunologyPublished by: -
3Staff View
ISSN: 1365-3083Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineNotes: Medial histocompatibility (H) antigens are weak H antigens, recognized by unrestricted T cells; they differ thus from both major and minor H antigens. An example, Qed-1, is described in detail, and other known medial H antigens of the mouse are reviewed. The structural and genetic relationships of major and medial H antigens and their role in T cell recognition are discussed.Type of Medium: Electronic ResourceURL: -
4Staff View
ISSN: 0169-4758Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
5Staff View
ISSN: 0169-4758Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
6Staff View
ISSN: 1365-3083Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MedicineNotes: T cells from spleens of mice infected with the erythrocytic stages of Plasmodium chabaudi chabaudi have been analysed with respect to their expression of surface molecules CD3, CD4 and CDS and T-cell receptor (TCR)αβ and γδ. The majority of T cells from infected mice were αβTCR +. However, there was an increase of approximately 8–10-fold in the proportion and total number of γδ T cells. Immunocytochemical analysis of sections of spleens taken from infected C57BL/6 mice during a primary infection showed that this increase took place particularly in the non-lymphoid areas. Within the αβ TCR+ T-cell population, both CD4+ T cells and CD8+ T cells were represented in proportions similar to those observed in normal uninfected mice. Stimulation of splenic T cells from infected mice with P. chabaudi-infected erythrocytes in vitro resulted ina blasted cell population composed predominantly of αβTTCR+ T cells with no preferential expansion of γβTCR+ T cells. There was no evidence of superantigen-like stimulation of T cells bearing particular Vβ chains of the TCR. The representation of the different Vβ chains within the population was not significantly different from that seen in uninfected mice.Type of Medium: Electronic ResourceURL: