Literature DB >> 7546405

Analysis of lymphocyte costimulation in vivo using transgenic and 'knockout' mice.

A H Sharpe1.   

Abstract

The use of transgenic technologies in the functional evaluation of the contributions of costimulatory pathways to T-cell activation in vivo has recently undergone a rapid expansion. During the past two years, mice deficient in costimulatory molecules and their receptors have been generated. These mice have revealed novel and critical in vivo functions of costimulatory pathways and have provided valuable models in which to test therapeutic strategies involving costimulatory pathway blockade. Transgenic mice constitutively expressing costimulatory molecules have provided insights into their role in peripheral tolerance.

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Year:  1995        PMID: 7546405     DOI: 10.1016/0952-7915(95)80115-4

Source DB:  PubMed          Journal:  Curr Opin Immunol        ISSN: 0952-7915            Impact factor:   7.486


  15 in total

1.  Cognate stimulatory B-cell-T-cell interactions are critical for T-cell help recruited by glycoconjugate vaccines.

Authors:  H K Guttormsen; A H Sharpe; A K Chandraker; A K Brigtsen; M H Sayegh; D L Kasper
Journal:  Infect Immun       Date:  1999-12       Impact factor: 3.441

Review 2.  CTLA-4 and tolerance: the biochemical point of view.

Authors:  Shunsuke Chikuma; Jeffrey A Bluestone
Journal:  Immunol Res       Date:  2003       Impact factor: 2.829

Review 3.  IL-10-producing and naturally occurring CD4+ Tregs: limiting collateral damage.

Authors:  Anne O'Garra; Pedro L Vieira; Paulo Vieira; Anne E Goldfeld
Journal:  J Clin Invest       Date:  2004-11       Impact factor: 14.808

4.  Thymocyte development is normal in CTLA-4-deficient mice.

Authors:  C A Chambers; D Cado; T Truong; J P Allison
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

5.  T-cell-mediated immunity to lymphocytic choriomeningitis virus in beta2-integrin (CD18)- and ICAM-1 (CD54)-deficient mice.

Authors:  J P Christensen; O Marker; A R Thomsen
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

6.  Modulation of experimental blood stage malaria through blockade of the B7/CD28 T-cell costimulatory pathway.

Authors:  A W Taylor-Robinson; E C Smith
Journal:  Immunology       Date:  1999-03       Impact factor: 7.397

7.  Branched O-linked oligosaccharides ectopically expressed in transgenic mice reduce primary T-cell immune responses.

Authors:  S Tsuboi; M Fukuda
Journal:  EMBO J       Date:  1997-11-03       Impact factor: 11.598

8.  Modulation of murine Lyme borreliosis by interruption of the B7/CD28 T-cell costimulatory pathway.

Authors:  M C Shanafelt; I Kang; S W Barthold; L K Bockenstedt
Journal:  Infect Immun       Date:  1998-01       Impact factor: 3.441

9.  Altered phenotype and function of dendritic cells in children with type 1 diabetes.

Authors:  F Angelini; E Del Duca; S Piccinini; V Pacciani; P Rossi; M L Manca Bitti
Journal:  Clin Exp Immunol       Date:  2005-11       Impact factor: 4.330

10.  Simultaneous cross-linking of CD6 and CD28 induces cell proliferation in resting T cells.

Authors:  L M Osorio; M Rottenberg; M Jondal; S C Chow
Journal:  Immunology       Date:  1998-03       Impact factor: 7.397

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