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Human T-Cell Memory

  • Conference paper
Immunological Memory

Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 159))

Abstract

The specificity and memory of immune responses sets them apart from all other physiological responses except those of the nervous system. These properties have long been recognised by immunologists, and while specificity is well accounted for by clonally distributed B- and T-cell receptors, the nature of immunological memory still poses many problems. While it has often been assumed that memory cells are long-lived and not dependent on continuous or repeated antigenic stimulation, this view has been challenged by recent data which suggest that persistence of memory is dependent on continued antigen drive (Gray and Skarvall 1988).

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References

  • Akbar AN, Terry LA, Timms A, Beverley PCL, Janossy G (1988) Loss of CD45R and gain of UCHL1 reactivity is a feature of primed T cells. J Immunol 140: 2171–2179

    PubMed  CAS  Google Scholar 

  • Arthur RP, Mason D (1986) T cells that help B cell responses to soluble antigen are distinguishable from those producing interleukin 2 on mitogenic or allogenec stimulation. J Exp Med 163: 774–786

    Article  PubMed  CAS  Google Scholar 

  • Ashwell JD, Chen C, Schwartz RH (1986) High frequency and non-random distribution of alloreactivity in T cell clones selected for recognition of foreign antigen in association with self class II molecules. J Immunol 136: 389–395

    PubMed  CAS  Google Scholar 

  • Beverley PCL, Terry L, Pickford A (1986) T cell subsets and function. In: Cinader B, Miller R (eds) Progress in immunology VI. Academic, Orlando, pp 941–948

    Google Scholar 

  • Blue ML, Daley JF, Levine H, Schlossman SF (1985) Lectin activation induces T4, T8 co-expression on peripheral blood T cells. In: Reinherz EL et al. (eds) Leucocyte typing II. Springer, Berlin Heidelberg, New York, pp 89–100

    Google Scholar 

  • Buckle A-M, Hogg N (1989) ICAM-1 expression on T cells. J Cell Biochem 13 A [Suppl] C109: 193

    Google Scholar 

  • Budd RC, Cerottini J-C, MacDonald HR (1987) Phenotypic identification of memory cytolytic T lymphocytes in a subset of Lyt-2+ cells. J Immunol 138: 1009–1013

    PubMed  CAS  Google Scholar 

  • Byrne JA, Butler JL, Cooper M (1988) Differential activation requirements for virgin and memory T cells. J Immunol 141: 3249–3256

    PubMed  CAS  Google Scholar 

  • Calvo C-F, Bernard A, Huet S, Leroy E, Boumsell L, Senik A (1986) Regulation of immunoglobulin synthesis by human T cell subsets as defined by anti-D44 monoclonal antibody within the CD4 + and CD8+ subpopulations. J Immunol 136: 1144–1149

    PubMed  CAS  Google Scholar 

  • Cavender DE, Haskard DO, Maliakkai D, Ziff M (1987) Separation and characterisation of human T cell subsets with varying degrees of adhesiveness for endothelial cells (EC). Arthritis Rheum 30: 29–32

    Google Scholar 

  • Cebra JJ, Komisar J-L, Schweitzer PA (1984) Ch isotype “switching” during normal B-lymphocyte development. Annu Rev Immunol 2: 493–548

    Article  PubMed  CAS  Google Scholar 

  • Charbonneau H, Tonks NK, Walsh KA, Fischer EH (1988). The leucocyte common antigen (CD45): a putative receptor-linked protein tyrosine phosphatase. Proc Natl Acad Sci USA 85: 7182–7186

    Article  PubMed  CAS  Google Scholar 

  • Corte G, Mingari MC, Moretta A, Damiani G, Moretta L, Bargellesi A (1982) Human T cell subpopulations defined by a monoclonal antibody. I. A small subset is responsible for proliferation to allogeneic cells or to soluble antigens and for helper activity for B. J Immunol 128:16–19

    PubMed  CAS  Google Scholar 

  • Crawford DH, Iliescu V, Edwards AJ, Beverley PCL (1983) Characterisation of Epstein Barr Virus- specific memory cells from the blood of seropositive individuals. J Cancer 47: 681–686

    Article  CAS  Google Scholar 

  • Cumano A, Dildrop R, Kocks C, Rajewsky K, Sablitzky F, Siekevitz M (1986) Mutation and selection of antibodies. In: Cinader B, Miller RG (eds) Progress in immunology VI. Academic, Orlando, pp 139–144

    Google Scholar 

  • Damle NK, Childs AL, Doyle LV (1987) Immunoregulatory T lymphocytes in man. Soluble antigen- specific suppressor-inducer T lymphocytes are derived from the CD4+ CD45R-p80+ subpopulation. J Immunol 139: 1501–1508

    PubMed  CAS  Google Scholar 

  • Evans RL, Breard JM, Lazarus H, Schlossman SF, Chess L (1977) Detection, isolation and functional characterisation of two human T cell subclasses bearing unique differentiation antigens. J Exp Med 145:221–228

    Article  PubMed  CAS  Google Scholar 

  • Gatenby PA, Kansas GS, Xian CY, Evans RL, Engleman EG (1982) Dissection of immunoregulatory subpopulations of T lymphocytes within the helper and suppressor sublineages in man. J Immunol 129: 1997–2000

    PubMed  CAS  Google Scholar 

  • Gray D, Skarvall H (1988) B-cell memory is short-lived in the absence of antigen. Nature 336: 70–72

    Article  PubMed  CAS  Google Scholar 

  • Hafler DA, Fox DA, Benjamin D, Weiner HL (1986) Antigen reactive memory cells are defined by Tal J Immunol 137: 414–418

    PubMed  CAS  Google Scholar 

  • Hedlund G, Dohlsten M, Sjogren HO, Carlsson R (1989) Maximal interferon-gamma production and early synthesis of interleukin-2 by CD4 + Cdw29 + CD45R-p80- human T lymphocytes. Immunology 66: 49–53

    PubMed  CAS  Google Scholar 

  • Hirayama K, Matsushita S, Kikuchi I, Iuchi M, Ohta N, Sasazuki T (1987) HLA-DQ is epistatic to HLA-DR in controlling the response to schistosomal antigens in humans. Nature 327: 426–429

    Article  PubMed  CAS  Google Scholar 

  • Hirohata S, Jelinek DF, Lipsky PE (1988) T cell dependent activation of B cell proliferation and differentiation by immobilized monoclonal antibodies to CD3. J Immunol 140: 3720–3733

    Google Scholar 

  • Huet S, Boumsell L, Dausset J, Degos L, Bernard A (1988) The required interaction between monocytes and peripheral blood T lymphocytes (T-PBL) upon activation via CD2 or CD3. Role of HLA class I molecules and the differential response of T-PBL subsets. Eur J Immunol 18: 1187–1194

    Article  PubMed  CAS  Google Scholar 

  • Leucocyte typing IV. Proceedings of the 4th international workshop on leucocyte differentiation antigens (in preparation)

    Google Scholar 

  • Landay A, Gartland GL, Clement LT (1983) Characterisation of a phenotypically distinct subpopulation of Leu 2 + cells that suppresses T cell proliferative responses. J Immunol 131:2757–2763

    PubMed  CAS  Google Scholar 

  • Ledbetter JA, Tonks NK, Fischer EH, Clark EA (1988) CD45 regulates signal transduction and lymphocyte activation by specific association with receptor molecules on T or B cells. Proc Natl Acad Sci USA 85: 8628–8634

    Article  PubMed  CAS  Google Scholar 

  • Lum LG, Orcutt-Thordarson N, Seineuret MC, Hansen JA (1982) In vitro regulation of immunoglobulin synthesis by T-cell subpopulations defined by a new human T-cell antigen (9.3). Cell Immunol 72: 122–129

    Article  PubMed  CAS  Google Scholar 

  • Merkenschlager M, Beverley PCL (1989) Evidence for differential expression of CD45 isoforms by precursors for memory dependent and independent cytotoxic responses: Human CD8 memory CTLp selectively express CD45RO (UCHL1). International Immunol 1: 450–459

    Article  CAS  Google Scholar 

  • Merkenschlager M, Terry L, Edwards R, Beverley PCL (1988) Limiting dilution analysis of proliferative responses in human lymphocyte populations defined by the monoclonal antibody UCHL1: implications for differential CD45 expression in T cells memory formation. Eur J Immunol 18: 1653–1659

    Article  PubMed  CAS  Google Scholar 

  • Meuer SC, Hussey RE, Fabbi M, Fox D, Acuto O, Fitzgerald KA, Hodgdon JP, Protentis JP, Schlossman SF (1984) Alternative pathway of T-cell activation: a functional role for the 50 kd T11 sheep erythrocyte receptor protein. Cell 36: 897–908

    Article  PubMed  CAS  Google Scholar 

  • Moretta L, Webb SR, Grossi CE, Lydyard PM, Cooper MD (1977) Functional analysis of two human T-cell subpopulations: help and suppression of B-cell responses by T cells bearing receptors for IgM or IgG. J Exp Med 146: 184–200

    Article  PubMed  CAS  Google Scholar 

  • Morimoto C (1988) CD4 + CD45R + cells are preferentially activated through the CD2 pathway. Eur J Immunol 18: 473–1478

    Article  Google Scholar 

  • Morimoto C, Letvin NL, Distaso JA, Aldrich WR, Schlossman SF (1985a) The isolation and characterisation of the human suppressor inducer T cell subset. J Immunol 134: 1508–1515

    PubMed  CAS  Google Scholar 

  • Morimoto C, Letvin NL, Boyd AW, Hagan M, Brown HM, Kornacki MM, Schlossman SF (1985b) The isolation and characterisation of the human helper inducer T cell. subset. J Immunol 134: 3762–3769

    PubMed  CAS  Google Scholar 

  • Morimoto C, Letvin NL, Distaso JA, Brown HM, Schlossman SF (1986) The cellular basis for the induction of antigen-specific T8 suppressor cells. Eur J Immunol 16: 198–204

    Article  PubMed  CAS  Google Scholar 

  • Mossmann TR, Cherwinski H, Bond MW, Giedlin MA, Coffman RL (1986) Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol 136: 2348–2357

    Google Scholar 

  • Nieda M, Juji T, Imao S, Minami M (1988) A role of HLA-DQ molecules of stimulator-adherent cells in the regulation of human autologous mixed lymphocyte reaction. J Immunol 141: 2975–2979

    PubMed  CAS  Google Scholar 

  • Paliard X, De Waal Malefijt R, Yssel H, Blanchard D, Chretien I, Abrams J, De Vries J, Spits H (1988) Simultaneous production of IL-2, IL-4, and IFN-γ by activated human CD4+ and CD8+ T cell clones. J Immunol 141: 849–855

    PubMed  CAS  Google Scholar 

  • Pizalis C, Kingsley G, Murphy J, Panayi G (1987) Abnormal distribution of the helper-inducer and suppressor-inducer T-lymphocyte-subset in the rheumatoid joint. Clin Immunol Immunopathol 45:252–258

    Article  Google Scholar 

  • Powrie F, Mason D (1988) The MRC OX-22- CD4+ T cells that help B cells in secondary immune responses derive from naive precursors with the MRC OX-22 + CD4+ phenotype. J Exp Med 169: 653

    Article  Google Scholar 

  • Reinherz EL, Schlossman SF (1980) The differentiation and function of human T lymphocytes. Cell 19:821–827

    Article  PubMed  CAS  Google Scholar 

  • Reinherz EL, Morimoto C, Penta AC, Schlossman SF (1980) Regulation of B cell immunoglobulin secretion by functional subsets of T lymphocytes in man. Eur J Immunol 10: 570–572

    Article  PubMed  CAS  Google Scholar 

  • Reinherz EL, Morimoto C, Fitzgerald KA, Hussey RE, Daley JF, Schlossmann SF (1982) Heterogeneity of human T4+ inducer T cells defined by a monoclonal antibody that delineates two functional subpopulations. J Immunol 126: 463–468

    Google Scholar 

  • Rotteveel FTM, Kokkelink I, Van Lier RAW, Kuenen B, Meager A, Miedema F, Lucas CJ (1988) Clonal analysis of functionally distinct human CD4 + T cell subsets. J Exp Med 168 : 1659–1674

    Article  PubMed  CAS  Google Scholar 

  • Salmon M, Kitas GD, Hill Gaston JS, Bacon PA (1988) Interleukin-2 production and response by helper T-cell subsets in man. Immunology 65: 81–85

    PubMed  CAS  Google Scholar 

  • Sanders ME, Makgoba MW, Sharrow SO, Stephany D, Springer A, Young HA, Shaw S (1988a) Human memory T lymphocytes express increased levels of three cell adhesion molecules (LFA-3, CD-2, LFA-1) and three other molecules (UCHL1, CDw29 and Pgp-1) and have enhanced IFN-γ production. J Immunol 140: 1401–1408

    PubMed  CAS  Google Scholar 

  • Sanders ME, Makgoba MW, Shaw S (1988b) Human naive and memory T cells: reinterpretation and further characterisation of helper-inducer and suppressor-inducer subsets. Immunol Today 9:195–198

    Article  PubMed  CAS  Google Scholar 

  • Serra HM, Krowka JF, Ledbetter JA, Pilarski LM (1988) Loss of CD45R (Lp220) represents a post- thymic T cell differentiation event. J Immunol 140: 1435–1442

    PubMed  CAS  Google Scholar 

  • Shaw S, Luce GEG, Quinones R, Gress RE, Springer TA, Sanders ME (1986) Two antigen- independent adhesion pathways used by human cytotoxic T cell clones. Nature 323: 262–265

    Article  PubMed  CAS  Google Scholar 

  • Smith S, Brown MH, Rowe D, Callard RE, Beverley PCL (1986) Functional subsets of human helper- inducer cells defined by a new mAb, UCHL1. Immunology 58: 63–70

    PubMed  CAS  Google Scholar 

  • Springer TA, Dunstin ML, Kishimoto TK, Marlin SD (1987) The lymphocyte function-associated LFA-1, CD2 and LFA-3 molecules: cell adhesion of the immune system. Annu Rev Immunol 5: 223–242

    Article  PubMed  CAS  Google Scholar 

  • Streuli M, Hall LR, Saga Y, Schlossman SF, Saito H (1987) Differential use of three exons generates at least five different mRNAs encoding human leucocyte common antigens. J Exp Med 166: 1548–1467

    Article  PubMed  CAS  Google Scholar 

  • Tedder TF, Clement LT, Cooper MD (1985) Human lymphocyte differentiation antigens HB-10 and HB-11. II Differential production of B cell growth and differentiation factors by distinct helper T cell subpopulations. J Immunol 134: 2983–2988

    PubMed  CAS  Google Scholar 

  • Tighe H, Clark M, Waldmann H (1987) Blocking of cytotoxic T cell function by monoclonal antibodies against the CD45 antigen (T200/Leukocyte-common) antigen. Transplantation 44: 818–823

    Article  PubMed  CAS  Google Scholar 

  • Yamada H, Martin PJ, Bean MA, Braun MP, Beatty PG, Sadamoto K, Hansen JA (1985) Monoclonal antibody 9.3 and anti-CD11 antibodies define reciprocal subsets of lymphocytes. Eur J Immunol 15: 1164–1168

    Article  PubMed  CAS  Google Scholar 

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© 1990 Springer-Verlag Berlin Heidelberg

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Beverley, P.C.L. (1990). Human T-Cell Memory. In: Gray, D., Sprent, J. (eds) Immunological Memory. Current Topics in Microbiology and Immunology, vol 159. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75244-5_7

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  • DOI: https://doi.org/10.1007/978-3-642-75244-5_7

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-75246-9

  • Online ISBN: 978-3-642-75244-5

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