Literature DB >> 11145669

Heterogeneity of the memory CD4 T cell response: persisting effectors and resting memory T cells.

M Ahmadzadeh1, S F Hussain, D L Farber.   

Abstract

Defining the cellular composition of the memory T cell pool has been complicated by an inability to distinguish effector and memory T cells. We present here an activation profile assay, using anti-CD3 and antigenic stimuli, that clearly distinguishes effector and memory CD4 T cells and defines subsets of long-lived memory CD4 T cells based on CD62 ligand (CD62L) expression. The CD62L(low) memory subset functionally resembles effector cells, exhibiting hyper-responsiveness to antigenic and anti-CD3 mediated stimuli, high proliferative capacity, and rapid activation kinetics. The CD62L(high) memory subset functionally resembles resting memory cells, exhibiting hyporesponsiveness to anti-CD3 stimuli, lower proliferative capacity, and slower activation kinetics. Our results indicate that the memory CD4 T cell pool is heterogeneous, consisting of persisting effectors and resting memory T cells.

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Year:  2001        PMID: 11145669     DOI: 10.4049/jimmunol.166.2.926

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  29 in total

1.  Functional plasticity of an antigen-specific memory CD4 T cell population.

Authors:  Mojgan Ahmadzadeh; Donna L Farber
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-21       Impact factor: 11.205

2.  Turning immunological memory into amnesia by depletion of dividing T cells.

Authors:  Bertrand Bellier; Véronique Thomas-Vaslin; Marie-Françoise Saron; David Klatzmann
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-21       Impact factor: 11.205

Review 3.  Immunological memory: lessons from the past and a look to the future.

Authors:  Donna L Farber; Mihai G Netea; Andreas Radbruch; Klaus Rajewsky; Rolf M Zinkernagel
Journal:  Nat Rev Immunol       Date:  2016-02       Impact factor: 53.106

4.  Ex vivo monitoring of antigen-specific CD4+ T cells after recall immunization with tetanus toxoid.

Authors:  Catherine Barbey; Estelle Pradervand; Nathalie Barbier; François Spertini
Journal:  Clin Vaccine Immunol       Date:  2007-07-18

5.  Flexibility accompanies commitment of memory CD4 lymphocytes derived from IL-4 locus-activated precursors.

Authors:  Eric Adeeku; Prathyusha Gudapati; Yanice Mendez-Fernandez; Luc Van Kaer; Mark Boothby
Journal:  Proc Natl Acad Sci U S A       Date:  2008-06-30       Impact factor: 11.205

Review 6.  Heterogeneous memory T cells in antiviral immunity and immunopathology.

Authors:  David Verhoeven; John R Teijaro; Donna L Farber
Journal:  Viral Immunol       Date:  2008-06       Impact factor: 2.257

7.  Donor-derived CD4(+)/CCR7(+) T-cell partial selective depletion does not alter acquired anti-infective immunity.

Authors:  B Choufi; J Trauet; S Thiant; M Labalette; I Yakoub-Agha
Journal:  Bone Marrow Transplant       Date:  2014-02-24       Impact factor: 5.483

8.  Early effector cells survive the contraction phase in malaria infection and generate both central and effector memory T cells.

Authors:  Michael M Opata; Victor H Carpio; Samad A Ibitokou; Brian E Dillon; Joshua M Obiero; Robin Stephens
Journal:  J Immunol       Date:  2015-04-24       Impact factor: 5.422

Review 9.  Biochemical signaling pathways for memory T cell recall.

Authors:  Donna L Farber
Journal:  Semin Immunol       Date:  2009-04       Impact factor: 11.130

10.  CD4 T cell memory derived from young naive cells functions well into old age, but memory generated from aged naive cells functions poorly.

Authors:  Laura Haynes; Sheri M Eaton; Eve M Burns; Troy D Randall; Susan L Swain
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

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