Literature DB >> 7522154

Differences in responsiveness to CD3 stimulation between naive and memory CD4+ T cells cannot be overcome by CD28 costimulation.

H Kuiper1, M Brouwer, M de Boer, P Parren, R A van Lier.   

Abstract

Activation of naive CD4+ T cells is essential for the induction of primary immune responses. However, this subset is less responsive to signaling via T cell receptor/CD3 (TcR/CD3) complex than memory CD4+ cells. For mitogenic activation of T cells, in addition to triggering of the TcR/CD3 complex, costimulatory signals are required that can be generated by surface structures present on the antigen-presenting cells. We investigated here whether differences in responsiveness to TcR/CD3 stimulation of naive and memory cells can be overcome by the costimulatory pathway B7/CD28. Using a B7-dependent system we show that even in the presence of optimal CD28 costimulation, CD4+ naive cells still have more stringent TcR/CD3 activation requirements than memory cells. Furthermore, titration of the B7 signal revealed that for activation of naive CD4+ cells a higher level of cross-linking of CD28 molecules is required than for memory cells. Thus, our results show that at least two signals are required for activation of both CD4+ memory and naive cells, but that for activation of naive cells higher cross-linking of both CD3 and CD28 molecules is necessary.

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Year:  1994        PMID: 7522154     DOI: 10.1002/eji.1830240903

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  9 in total

Review 1.  Qualitative differences between naïve and memory T cells.

Authors:  Marion Berard; David F Tough
Journal:  Immunology       Date:  2002-06       Impact factor: 7.397

2.  Immune memory in CD4+ CD45RA+ T cells.

Authors:  D Richards; M D Chapman; J Sasama; T H Lee; D M Kemeny
Journal:  Immunology       Date:  1997-07       Impact factor: 7.397

3.  LFA-1 is a key determinant for preferential infection of memory CD4+ T cells by human immunodeficiency virus type 1.

Authors:  Mélanie R Tardif; Michel J Tremblay
Journal:  J Virol       Date:  2005-11       Impact factor: 5.103

4.  Major histocompatibility complex class II-expressing endothelial cells induce allospecific nonresponsiveness in naive T cells.

Authors:  F M Marelli-Berg; R E Hargreaves; P Carmichael; A Dorling; G Lombardi; R I Lechler
Journal:  J Exp Med       Date:  1996-04-01       Impact factor: 14.307

5.  Low CD3+CD28-induced interleukin-2 production correlates with decreased reactive oxygen intermediate formation in neonatal T cells.

Authors:  S Kilpinen; M Hurme
Journal:  Immunology       Date:  1998-06       Impact factor: 7.397

6.  The modulation of PPARγ1 and PPARγ2 mRNA expression by ciglitazone in CD3/CD28-activated naïve and memory CD4+ T cells.

Authors:  Mohd Nor Norazmi; Rafeezul Mohamed; Asma Abdullah Nurul; Nik Soriani Yaacob
Journal:  Clin Dev Immunol       Date:  2012-04-02

7.  Endothelial cells modify the costimulatory capacity of transmigrating leukocytes and promote CD28-mediated CD4(+) T cell alloactivation.

Authors:  M D Denton; C S Geehan; S I Alexander; M H Sayegh; D M Briscoe
Journal:  J Exp Med       Date:  1999-08-16       Impact factor: 14.307

8.  Role of acid sphingomyelinase bioactivity in human CD4+ T-cell activation and immune responses.

Authors:  A Bai; E Kokkotou; Y Zheng; S C Robson
Journal:  Cell Death Dis       Date:  2015-07-23       Impact factor: 8.469

Review 9.  The role of CD4 T cells in the pathogenesis of multiple sclerosis.

Authors:  Tanuja Chitnis
Journal:  Int Rev Neurobiol       Date:  2007       Impact factor: 3.230

  9 in total

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