Literature DB >> 12018463

Dissecting the complexity of the memory T cell response.

Donna L Farber1, Mojgan Ahmadzadeh.   

Abstract

Memory immune responses are classically attributed to the reactivation of long-lived, antigen-specific T lymphocytes that persist in a quiescent state. Determining mechanisms for the generation of memory T cells and dissecting the functional nature of the memory T cell pool has been encumbered by an inability to distinguish recently activated effector T cells from memory T cells. We have established new activation and biochemical criteria that distinguish effector and memory T cells and have applied these criteria to follow memory generation from activated cells in vivo. We found that the resultant memory T cell pool is heterogeneous and consists of effector-like and resting memory-like subsets that differ in expression of the homing receptor, CD62L. We discuss these findings in the context of memory T cell heterogeneity identified in human and mouse systems. These results suggest that more than one type of previously activated T cell can mediate recall or memory immune responses and that elucidating the fundamental phenotypic and functional features of memory T cell subsets is therefore critical to deciphering the complex nature of the memory immune response.

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Year:  2002        PMID: 12018463     DOI: 10.1385/IR:25:3:247

Source DB:  PubMed          Journal:  Immunol Res        ISSN: 0257-277X            Impact factor:   4.505


  78 in total

1.  Effector CD4 T cells are biochemically distinct from the memory subset: evidence for long-term persistence of effectors in vivo.

Authors:  M Ahmadzadeh; S F Hussain; D L Farber
Journal:  J Immunol       Date:  1999-09-15       Impact factor: 5.422

2.  Activated and memory CD8+ T cells can be distinguished by their cytokine profiles and phenotypic markers.

Authors:  M K Slifka; J L Whitton
Journal:  J Immunol       Date:  2000-01-01       Impact factor: 5.422

3.  Class II-independent generation of CD4 memory T cells from effectors.

Authors:  S L Swain; H Hu; G Huston
Journal:  Science       Date:  1999-11-12       Impact factor: 47.728

4.  Transforming growth factor-beta and IL-4 cause helper T cell precursors to develop into distinct effector helper cells that differ in lymphokine secretion pattern and cell surface phenotype.

Authors:  S L Swain; G Huston; S Tonkonogy; A Weinberg
Journal:  J Immunol       Date:  1991-11-01       Impact factor: 5.422

5.  Antigen-specific development of primary and memory T cells in vivo.

Authors:  M G McHeyzer-Williams; M M Davis
Journal:  Science       Date:  1995-04-07       Impact factor: 47.728

Review 6.  Immunological memory and protective immunity: understanding their relation.

Authors:  R Ahmed; D Gray
Journal:  Science       Date:  1996-04-05       Impact factor: 47.728

7.  A comparison of T cell memory against the same antigen induced by virus versus intracellular bacteria.

Authors:  A F Ochsenbein; U Karrer; P Klenerman; A Althage; A Ciurea; H Shen; J F Miller; J L Whitton; H Hengartner; R M Zinkernagel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

8.  Generation and biochemical analysis of human effector CD4 T cells: alterations in tyrosine phosphorylation and loss of CD3zeta expression.

Authors:  S Krishnan; V G Warke; M P Nambiar; H K Wong; G C Tsokos; D L Farber
Journal:  Blood       Date:  2001-06-15       Impact factor: 22.113

9.  Memory T cells are anergic to the superantigen staphylococcal enterotoxin B.

Authors:  W T Lee; E S Vitetta
Journal:  J Exp Med       Date:  1992-08-01       Impact factor: 14.307

10.  Turnover of naive- and memory-phenotype T cells.

Authors:  D F Tough; J Sprent
Journal:  J Exp Med       Date:  1994-04-01       Impact factor: 14.307

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  6 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

Review 2.  The effector to memory transition of CD4 T cells.

Authors:  K Kai McKinstry; Tara M Strutt; Susan L Swain
Journal:  Immunol Res       Date:  2008       Impact factor: 2.829

3.  Engraftment of human central memory-derived effector CD8+ T cells in immunodeficient mice.

Authors:  Xiuli Wang; Carolina Berger; ChingLam W Wong; Stephen J Forman; Stanley R Riddell; Michael C Jensen
Journal:  Blood       Date:  2010-12-01       Impact factor: 22.113

4.  Evaluation of CD62L expression as a marker for vaccine-elicited memory cytotoxic T lymphocytes.

Authors:  Shawn S Jackson; Jörn E Schmitz; Marcelo J Kuroda; Paul F McKay; Shawn M Sumida; Kristi L Martin; Faye Yu; Michelle A Lifton; Darci A Gorgone; Norman L Letvin
Journal:  Immunology       Date:  2005-12       Impact factor: 7.397

5.  Changes in Gene Expression and Metabolism in the Testes of the Rat following Spinal Cord Injury.

Authors:  Ryan D Fortune; Raymond J Grill; Christine Beeton; Mark Tanner; Redwan Huq; David S Loose
Journal:  J Neurotrauma       Date:  2016-12-02       Impact factor: 5.269

Review 6.  Allo-reactive T cells for the treatment of hematological malignancies.

Authors:  J H F Falkenburg; I Jedema
Journal:  Mol Oncol       Date:  2015-10-24       Impact factor: 6.603

  6 in total

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