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Development of Lymphocyte Responses to Herpes Simplex Virus Following Neonatal Infection

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Immunology of the Neonate

Abstract

Children with congenital cytomegalovirus infection continue to shed the virus in their urine for several years, and survivors of neonatal herpes simplex virus (HSV) infection have recurrent crops of skin vesicles caused by HSV in infancy. Both observations suggest that immune responses to these viruses are limited following congenital or neonatal infection. Affected children have few T cells in their blood, which proliferate in response to the infecting virus (Hayward et al. 1984a). However, the presence of first IgM and later IgG antibodies to HSV in their serum indicates that they have developed specific immunity and suggests that they have T cells capable of providing help to B cells (Hayward et al. 1984b).

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References

  • Abo T, Cooper MD, Balch CM (1982) Postnatal expansion of the natural killer and killer cell population in humans identified by the monoclonal HNK 1 antibody. J Exp Med 155: 321–326.

    Article  PubMed  CAS  Google Scholar 

  • Bailey J, Schacter B (1985) Stimulation of cord and adult NK cells. Pediatr Res (in press)

    Google Scholar 

  • Biron CA, Welsh RM (1985) Blastogenesis of natural killer cell in vivo results in progeny cells with the capacity for continued proliferation. Fed Proc 44: 1314 (Abstract # 5282)

    Google Scholar 

  • Bishop GA, Marlin SC, Schwartz SA, Glorioso JC (1984) Human natural killer cell recognition of herpes simplex virus type I glycoproteins: specificity analysis with the use of monoclonal antibodies and antigenic variants. J Immunol 133: 2206–2209.

    PubMed  CAS  Google Scholar 

  • Bukowski JF, Warner JF, Dennert G, Welsh RM (1985) Adoptive transfer studies demonstrating the anti-viral effects of natural killer cells in vivo. J Exp Med 161: 40–52.

    Article  PubMed  CAS  Google Scholar 

  • Chilmonczyk BA, Levon M J, McDuffi R, Hayward AR (1985) Characterization of the human newborn response to herpesvirus antigen. J Immunol 134: 4184–4188.

    PubMed  CAS  Google Scholar 

  • Collins MKL, Goodfellow PN, Spurr NK, Solomon E, Tanigawa T, Tonegawa S, Owen MJ (1985) The human T cell receptor β-chain gene maps to chromosome 14. Nature 314: 273–274.

    Article  PubMed  CAS  Google Scholar 

  • Corey L, Adams HG, Brown ZA, Holmes KK (1983) Genital herpes simplex infections: clinical manifestations, course and complications. Ann Intern 998: 958–972.

    Google Scholar 

  • Fitzgerald PA, Mendelsohn M, Lopez C (1985) Human natural killer cells limit replication of herpes simplex virus type 1 in vitro. J Immunol 134: 2666–2672.

    PubMed  CAS  Google Scholar 

  • Harrison CJ, Waner JL (1985) Natural killer cell activity in infants and children excreting cytomegalovirus. J Infect Dis 151: 301–307.

    Article  PubMed  CAS  Google Scholar 

  • Hayward AR, Malmberg S (1984) Response of human newborn lymphocytes to alloantigen: lack of evidence for suppression induction. Pediatr Res 18: 414–419.

    Article  PubMed  CAS  Google Scholar 

  • Hayward AR, Herberger M, Levin M (1984a) Reduced cytomegalovirus (CMV) responder T cell frequency in congenital CMV infection. In: Rapp F (ed) Herpesvirus. Liss, New York p 211.

    Google Scholar 

  • Hayward AR, Herberger MJ, Groothuis J, Levin MJ (1984b) Specific immunity after congenital or neonatal infection with cytomegalovirus or herpes simplex virus. J Immunol 133: 2469–2473.

    PubMed  CAS  Google Scholar 

  • Hayward AR, Lazslo M, Levin M (1984c) Suppression of HSV proliferation in fibroblast monolayers by HLA matched and unmatched mononuclear cells. Proc. 16th Leukocyte Culture Conference.

    Google Scholar 

  • Henney CS, Kuribayashi K, Kern DE, Gillis S (1981) Interleukin 2 augments natural killer cell activity. Nature 291: 335–338.

    Article  PubMed  CAS  Google Scholar 

  • Herberman RB, Ortaldo JR, Barnard G (1979) Augmentation by interferon of human natural and antibody dependent cell mediated cytotoxicity. Nature 277: 221–223.

    Article  PubMed  CAS  Google Scholar 

  • Hoffman AA, Hayward AR, Kurnick JT, De Freitas E, McGregor J, Harbeck RJ (1981) Presentation of antigen by human newborn monocytes to maternal tetanus toxoid specific T cell blasts. J Clin Immunol 1: 217.

    Article  Google Scholar 

  • Kennedy RC, Adlerstorthz K, Burns JW, Henkel RD, Dressman GR (1984) Antiidiotype modulation of herpes simplex virus infection leading to increased pathogenicity. J Virol 50: 951–953.

    PubMed  CAS  Google Scholar 

  • Kohl S (1984) Neonatal herpes. In: Ogra PL (ed) Neonatal infections. Grune and Stratton, New York.

    Google Scholar 

  • Kohl S, Bigelow RH, Loo LS (1984) Ontogeny of protection of neonatal mice from lethal herpes simplex virus infection by human leukocytes, antiviral antibody and recombinant α interferon. Pediatr Res 18: 1164–1167.

    Article  PubMed  CAS  Google Scholar 

  • Kohl S, Loo LS, Gonik B (1984) Analysis in human neonates of defective antibody-dependent cellular cytotoxicity and natural killer cytotoxicity to herpes simplex. J Infect Dis 150: 14.

    Article  PubMed  CAS  Google Scholar 

  • Lanier LL, Le AM, Phillips JH, Warner NL, Babcock GF (1983) Subopulations of human natural killer cells defined by expression of the Leu-7 (HNK-1) and Leu-11 (NK-15) antigens. J Immunol 131: 1789–1796.

    PubMed  CAS  Google Scholar 

  • Larsen HS, Feng MF, Horohov DW, Moore RN, Rouse BT (1984) Role of T-lymphocyte subsets in recovery from herpes simplex virus infection. J Virol 50: 56–59.

    PubMed  CAS  Google Scholar 

  • Lopez C, Kirkpatrick D, Read SE, Fitzgerald PA, Pitt J, Pahwa S, Ching CY, Smithwick EM (1983) Correlation between low natural killing of fibroblasts infected with herpes simplex virus type I and susceptibility to herpes virus infections. J Infect Dis 147: 1030–1035.

    Article  PubMed  CAS  Google Scholar 

  • Miyawaki T, Seki H, Taga K, Sato H, Taniguchi N (1985) Dissociated production of interleukin-2 and immune (γ) interferon by phytohaemagglutinin-stimulated lymphocytes in healthy infants. Clin Exp Immunol 59: 505–511.

    PubMed  CAS  Google Scholar 

  • Nair MPN, Schwartz SA, Menon M (1985) Decreased natural and antibody-dependent cellular cytotoxicity is associated with decreased production of natural killer cytotoxic factors and interferon in neonates. Pediatr Res 19: 279A (# 1011)

    Article  Google Scholar 

  • Nash AA, Phelan J, Woldy P (1981) Cell-mediated immunity in herpes simplex virus infected mice: H2 mapping of the delayed type hypersensitivity response and the antiviral T cell response. J Immunol 126: 1260–1262.

    PubMed  CAS  Google Scholar 

  • Oldstone MBA, Rodriquez M, Daughaday WH, Lampert PW (1984) Viral perturbation of endocrine function: disordered cell function leads to disturbed homeostasis and disease. Nature 307: 278–280.

    Article  PubMed  CAS  Google Scholar 

  • Pass RF, Dworsky ME, Whithley RJ, August AM, Stagno S, Alford CA (1981) Specific lymphocyte blastogenic responses in children with cytomegalovirus and herpes simplex virus infections acquired early in infancy. Infect Immunol 34: 166–170.

    CAS  Google Scholar 

  • Quinnan GV, Manischiewitz JE (1978) The role of natural killer cells and antibody-dependent cell mediated cytotoxicity during murine cytomegalovirus infection. J Exp Med 150: 1549.

    Article  Google Scholar 

  • Reinherz EL, O’Brien C, Rosenthal P, Schlosssman SF (1980) The cellular basis for viral induced immunodeficiency: analysis by monoclonal antibodies. J Immunol 125: 1269–1274.

    PubMed  CAS  Google Scholar 

  • Rinaldo CR, Richter BS, Black PH, Callery R, Chess C, Hirsch MS (1978) Replication of herpes simplex virus and cytomegalovirus in human leukocytes. J Immunol 120: 130–136.

    PubMed  Google Scholar 

  • Simmons A, Nash AA (1985) Role of antibody in primary and recurrent herpes simplex virus infection. J Virol 53: 944–948.

    PubMed  CAS  Google Scholar 

  • Stiehm ER, Sztein MB, Steeg PS, Mann D, Newland C, Blaese M, Oppenheim JJ (1984) Deficient DR antigen expression of human cord blood monocytes: reversal with lymphokines. Clin Immunol Immunopathol 30: 430–436.

    Article  PubMed  CAS  Google Scholar 

  • Suez D, Hayward AR (1985) Phenotyping of proliferating cells in cultures of human lymphocytes. J Immunol Methods 78: 49–57.

    Article  PubMed  CAS  Google Scholar 

  • Sullivan JL, Barry DW, Alabrecht P, Lucas SJ (1975) Inhibition of lymphocyte stimulation by measles virus. J Immunol 114: 1458–1462.

    PubMed  CAS  Google Scholar 

  • Trinchieri G, Matsumoto-Kobayashi M, Clark SC, Seehra S, London L, Perussia B (1984) Response of resting human peripheral blood natural killer cells to interleukin 2. J Exp Med 160: 1147–1169.

    Article  PubMed  CAS  Google Scholar 

  • Wilson CB, Westall J (1985) Lymphokine-dependent macrophage activation in newborns. Pediatr Res 19: 284(a)

    Google Scholar 

  • Yeager AS, Arvin AM, Urbani LE, Kemp JA (1980) Relationship of antibody to outcome in neonatal herpes simplex infections. Infect Immun 29: 532–538.

    PubMed  CAS  Google Scholar 

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© 1987 Springer-Verlag Berlin Heidelberg

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Hayward, A., Leibson, P., Arvin, A. (1987). Development of Lymphocyte Responses to Herpes Simplex Virus Following Neonatal Infection. In: Burgio, G.R., Hanson, L.Ã…., Ugazio, A.G. (eds) Immunology of the Neonate. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71094-0_12

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  • DOI: https://doi.org/10.1007/978-3-642-71094-0_12

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-71096-4

  • Online ISBN: 978-3-642-71094-0

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