Immunosuppression is the major cause of infant death associated with acute measles and therefore of substantial clinical importance. Major hallmarks of this generalized modulation of immune functions are (1) lymphopenia, (2) a prolonged cytokine imbalance consistent with suppression of cellular immunity to secondary infections, and (3) silencing of peripheral blood lymphocytes, which cannot expand in response to ex vivo stimulation. Lymphopenia results from depletion, which can occur basically at any stage of lymphocyte development, and evidently, expression of the major MV receptor CD150 plays an important role in targeting these cells. Virus transfer to T cells is thought to be mediated by dendritic cells (DCs), which are considered central to the induction of T cell silencing and functional skewing. As a consequence of MV interaction, viability and functional differentiation of DCs and thereby their expression pattern of co-stimulatory molecules and soluble mediators are modulated. Moreover, MV proteins expressed by these cells actively silence T cells by interfering with signaling pathways essential for T cell activation.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Addae MM, Komada Y, Zhang XL, Sakurai M (1995) Immunological unresponsiveness and apop-totic cell death of T cells in measles virus infection. Acta Paediatr Jpn 37:308–314
Addae MM, Komada Y, Taniguchi K, Kamiya T, Osei-Kwasi M et al (1998) Surface marker patterns of T cells and expression of interleukin-2 receptor in measles infection. Acta Paediatr Jpn 40:7–13
Arneborn P, Biberfeld G, Forsgren M, von Stedingk LV (1983) Specific and non-specific B cell activation in measles and varicella. Clin Exp Immunol 51:165–172
Arrieumerlou C, Meyer T (2005) A local coupling model and compass parameter for eukaryotic chemotaxis. Dev Cell 8:215–227
Asselin-Paturel C, Trinchieri G (2005) Production of type I interferons: plasmacytoid dendritic cells and beyond. J Exp Med 202:461–465
Astier A, Trescol-Biemont MC, Azocar O, Lamouille B, Rabourdin-Combe C (2000) Cutting edge: CD46, a new costimulatory molecule for T cells, that induces p120CBL and LAT phos-phorylation. J Immunol 164:6091–6095
Atabani SF, Byrnes AA, Jaye A, Kidd IM, Magnusen AF et al (2001) Natural measles causes prolonged suppression of interleukin-12 production. J Infect Dis 184:1–9
Aversa G, Carballido J, Punnonen J, Chang CC, Hauser T et al (1997) SLAM and its role in T cell activation and Th cell responses. Immunol Cell Biol 75:202–205
Avota E, Avots A, Niewiesk S, Kane LP, Bommhardt U et al (2001) Disruption of Akt kinase activation is important for immunosuppression induced by measles virus. Nat Med 7:725–731
Avota E, Muller N, Klett M, Schneider-Schaulies S (2004) Measles virus interacts with and alters signal transduction in T-cell lipid rafts. J Virol 78:9552–9559
Avota E, Harms H, Schneider-Schaulies S (2006) Measles virus induces expression of SIP110, a constitutively membrane clustered lipid phosphatase, which inhibits T cell proliferation. Cell Microbiol 8:1826–1839
Banchereau J, Steinman RM (1998) Dendritic cells and the control of immunity. Nature 392(6673): 245–252
Bieback K, Lien E, Klagge IM, Avota E, Schneider-Schaulies J et al (2002) Hemagglutinin protein of wild-type measles virus activates toll-like receptor 2 signaling. J Virol 76:8729–8736
Black FL, Berman LL, Borgono JM, Capper RA, Carvalho AA et al (1986) Geographic variation in infant loss of maternal measles antibody and in prevalence of rubella antibody. Am J Epidemiol 124:442–452
Borrow P, Oldstone MB (1995) Measles virus-mononuclear cell interactions. Curr Top Microbiol Immunol 191:85–100
Browning MB, Woodliff JE, Konkol MC, Pati NT, Ghosh S et al (2004) The T cell activation marker CD150 can be used to identify alloantigen-activated CD4(+)25+ regulatory T cells. Cell Immunol 227:129–139
Burns S, Hardy SJ, Buddle J, Yong KL, Jones GE et al (2004) Maturation of DC is associated with changes in motile characteristics and adherence. Cell Motil Cytoskeleton 57:118–132
Cacciotti P, Barbone D, Porta C, Altomare DA, Testa JR et al (2005) SV40-dependent AKT activity drives mesothelial cell transformation after asbestos exposure. Cancer Res 65:5256– 5262
Cameron P, Pope M, Granelli-Piperno A, Steinman RM (1996) Dendritic cells and the replication of HIV-1. J Leukoc Biol 59:158–171
Carsillo T, Zhang X, Vasconcelos D, Niewiesk S, Oglesbee M (2006) A single codon in the nucleocapsid protein C terminus contributes to in vitro and in vivo fitness of Edmonston measles virus. J Virol 80:2904–2912
Condack C, Grivel JC, Devaux P, Margolis L, Cattaneo R (2007) Measles virus vaccine attenuation: suboptimal infection of lymphatic tissue and tropism alteration. J Infect Dis 196:541–549
Dawson CW, Tramountanis G, Eliopoulos AG, Young LS (2003) Epstein-Barr virus latent membrane protein 1 (LMP1) activates the phosphatidylinositol 3-kinase/Akt pathway to promote cell survival and induce actin filament remodeling. J Biol Chem 278:3694–3704
de Swart RL, Ludlow M, de Witte L, Yanagi Y, van Amerongen G et al (2007) Predominant infection of CD150(+) lymphocytes and dendritic cells during measles virus infection of macaques. PLoS Pathog 3:e178
de Witte L, Abt M, Schneider-Schaulies S, van Kooyk Y, Geijtenbeek TB (2006) Measles virus targets DC-SIGN to enhance dendritic cell infection. J Virol 80:3477–3486
Dollimore N, Cutts F, Binka FN, Ross DA, Morris SS et al (1997) Measles incidence, case fatality, and delayed mortality in children with or without vitamin A supplementation in rural Ghana. Am J Epidemiol 146:646–654
Dorig RE, Marcil A, Chopra A, Richardson CD (1993) The human CD46 molecule is a receptor for measles virus (Edmonston strain). Cell 75:295–305
Dubois B, Lamy PJ, Chemin K, Lachaux A, Kaiserlian D (2001) Measles virus exploits dendritic cells to suppress CD4+ T-cell proliferation via expression of surface viral glycoproteins independently of T-cell trans-infection. Cell Immunol 214:173–183
Dunster LM, Schneider-Schaulies J, Loffler S, Lankes W, Schwartz-Albiez R et al (1994) Moesin: a cell membrane protein linked with susceptibility to measles virus infection. Virology 198:265–274
Ebihara T, Masuda H, Akazawa T, Shingai M, Kikuta H et al (2007) Induction of NKG2D ligands on human dendritic cells by TLR ligand stimulation and RNA virus infection. Int Immunol 19:1145–1155
Engelking O, Fedorov LM, Lilischkis R, ter Meulen V, Schneider-Schaulies S (1999) Measles virus-induced immunosuppression in vitro is associated with deregulation of G1 cell cycle control proteins. J Gen Virol 80:1599–1608
Erlenhoefer C, Wurzer WJ, Loffler S, Schneider-Schaulies S, ter Meulen V et al (2001) CD150 (SLAM) is a receptor for measles virus but is not involved in viral contact-mediated proliferation inhibition. J Virol 75:4499–4505
Esolen LM, Ward BJ, Moench TR, Griffin DE (1993) Infection of monocytes during measles. J Infect Dis 168:47–52
Forthal DN, Aarnaes S, Blanding J, de la Maza L, Tilles JG (1992) Degree and length of viremia in adults with measles. J Infect Dis 166:421–424
Fugier-Vivier I, Servet-Delprat C, Rivailler P, Rissoan MC, Liu YJ et al (1997) Measles virus suppresses cell-mediated immunity by interfering with the survival and functions of dendritic and T cells. J Exp Med 186:813–823
Fujinami RS, Sun X, Howell JM, Jenkin JC, Burns JB (1998) Modulation of immune system function by measles virus infection: role of soluble factor and direct infection. J Virol 72:9421–9427
Geier SJ, Algate PA, Carlberg K, Flowers D, Friedman C et al (1997) The human SHIP gene is differentially expressed in cell lineages of the bone marrow and blood. Blood 89:1876–1885
Geijtenbeek TB, Kwon DS, Torensma R, van Vliet SJ, van Duijnhoven GC et al (2000) DC-SIGN, a dendritic cell-specific HIV-1-binding protein that enhances trans-infection of T cells. Cell 100:587–597
Geijtenbeek TB, van Kooyk Y (2003a) DC-SIGN: a novel HIV receptor on DCs that mediates HIV-1 transmission. Curr Top Microbiol Immunol 276:31–54
Geijtenbeek TB, van Kooyk Y (2003b) Pathogens target DC-SIGN to influence their fate DC-SIGN functions as a pathogen receptor with broad specificity. Apmis 111:698–714
Griffin DE (1995) Immune responses during measles virus infection. Curr Top Microbiol Immunol 191:117–134
Griffin DE, Ward BJ (1993) Differential CD4 T cell activation in measles. J Infect Dis 168:275–281
Gringhuis SI, den Dunnen J, Litjens M, van Het Hof B, van Kooyk Y et al (2007) C-type lectin DC-SIGN modulates Toll-like receptor signaling via Raf-1 kinase-dependent acetylation of transcription factor NF-kappaB. Immunity 26:605–616
Grosjean I, Caux C, Bella C, Berger I, Wild F et al (1997) Measles virus infects human dendritic cells and blocks their allostimulatory properties for CD4+ T cells. J Exp Med 186:801–812
Hahm B, Arbour N, Naniche D, Homann D, Manchester M et al (2003) Measles virus infects and suppresses proliferation of T lymphocytes from transgenic mice bearing human signaling lymphocytic activation molecule. J Virol 77:3505–3515
Hahm B, Arbour N, Oldstone MB (2004) Measles virus interacts with human SLAM receptor on dendritic cells to cause immunosuppression. Virology 323:292–302
Heaney J, Barrett T, Cosby SL (2002) Inhibition of in vitro leukocyte proliferation by morbillivi-ruses. J Virol 76:3579–3584
Helin E, Salmi AA, Vanharanta R, Vainionpaa (1999) Measles virus replication in cells of myelo-monocytic lineage is dependent on cellular differentiation stage. Virology 253:35–42
Herschke F, Plumet S, Duhen T, Azocar O, Druelle J et al (2007) Cell—cell fusion induced by measles virus amplifies the type I interferon response. J Virol 81:12859–12871
Hirano A, Yang Z, Katayama Y, Korte-Sarfaty J, Wong TC (1999) Human CD46 enhances nitric oxide production in mouse macrophages in response to measles virus infection in the presence of gamma interferon: dependence on the CD46 cytoplasmic domains. J Virol 73:4776–4785
Hsu EC, Iorio C, Sarangi F, Khine AA, Richardson CD (2001) CDw150 (SLAM) is a receptor for a lymphotropic strain of measles virus and may account for the immunosuppressive properties of this virus. Virology 279:9–21
Hussey GD, Goddard EA, Hughes J, Ryon JJ, Kerran M et al (1996) The effect of Edmonston-Zagreb and Schwarz measles vaccines on immune response in infants. J Infect Dis 173:1320–1326
Jolly C, Mitar I, Sattentau QJ (2007) Adhesion molecule interactions facilitate human immunodeficiency virus type 1-induced virological synapse formation between T cells. J Virol 81:13916–13921
Kaiserlian D, Grosjean I, Caux C (1997) Infection of human dendritic cells by measles virus induces immune suppression. Adv Exp Med Biol 417:421–423
Karp CL, Wysocka M, Wahl LM, Ahearn JM, Cuomo PJ et al (1996) Mechanism of suppression of cell-mediated immunity by measles virus. Science 273(5272):228–231
Katz M (1995) Clinical spectrum of measles. Curr Top Microbiol Immunol 191:1–12
Kemper C, Chan AC, Green JM, Brett KA, Murphy KM et al (2003) Activation of human CD4+ cells with CD3 and CD46 induces a T-regulatory cell 1 phenotype. Nature 421(6921): 388–392
Kemper C, Verbsky JW, Price JD, Atkinson JP (2005) T-cell stimulation and regulation: with complements from CD46. Immunol Res 32:31–44
Kiel MJ, Yilmaz OH, Iwashita T, Yilmaz OH, Terhorst C et al (2005) SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells. Cell 121:1109–1121
Klagge IM, ter Meulen V, Schneider-Schaulies S (2000) Measles virus-induced promotion of dendritic cell maturation by soluble mediators does not overcome the immunosuppressive activity of viral glycoproteins on the cell surface. Eur J Immunol 30:2741–2750
Klagge IM, Abt M, Fries B, Schneider-Schaulies S (2004) Impact of measles virus dendritic-cell infection on Th-cell polarization in vitro. J Gen Virol 85:3239–3247
Kobune F, Takahashi H, Terao K, Ohkawa T, Ami Y et al (1996) Nonhuman primate models of measles. Lab Anim Sci 46:315–320
Kruse M, Meinl E, Henning G, Kuhnt C, Berchtold S et al (2001) Signaling lymphocytic activation molecule is expressed on mature CD83+ dendritic cells and is up-regulated by IL-1 beta. J Immunol 167:1989–1995
Laine D, Trescol-Biemont MC, Longhi S, Libeau G, Marie JC et al (2003) Measles virus (MV) nucleoprotein binds to a novel cell surface receptor distinct from FcgammaRII via its C-termi-nal domain: role in MV-induced immunosuppression. J Virol 77:11332–11346
Laine D, Bourhis JM, Longhi S, Flacher M, Cassard L et al (2005) Measles virus nucleoprotein induces cell-proliferation arrest and apoptosis through NTAIL-NR and NCORE-FcgammaRIIB1 interactions, respectively. J Gen Virol 86:1771–1784
Lennon JL, Black FL (1986) Maternally derived measles immunity in era of vaccine-protected mothers. J Pediatr 108:671–676
Makhortova NR, Askovich P, Patterson CE, Gechman LA, Gerard NP et al (2007) Neurokinin-1 enables measles virus trans-synaptic spread in neurons. Virology 362:235–244
Manchester M, Smith KA, Eto DS, Perkin HB, Torbett BE (2002) Targeting and hematopoietic suppression of human CD34+ cells by measles virus. J Virol 76:6636–6642
Marie JC, Kehren J, Trescol-Biemont MC, Evlashev A, Valentin H et al (2001) Mechanism of measles virus-induced suppression of inflammatory immune responses. Immunity 14:69–79
Marie JC, Astier AL, Rivailler P, Rabourdin-Combe C, Wild TF et al (2002) Linking innate and acquired immunity: divergent role of CD46 cytoplasmic domains in T cell induced inflammation. Nat Immunol 3:659–666
Marie JC, Saltel F, Escola JM, Jurdic P, Wild TF et al (2004) Cell surface delivery of the measles virus nucleoprotein: a viral strategy to induce immunosuppression. J Virol 78:11952–11961
McChesney MB, Fujinami RS, Lerche NW, Marx PA, Oldstone MB (1989) Virus-induced immu-nosuppression: infection of peripheral blood mononuclear cells and suppression of immu-noglobulin synthesis during natural measles virus infection of rhesus monkeys. J Infect Dis 159:757–760
McChesney MB, Miller CJ, Rota PA, Zhu YD, Antipa L et al (1997) Experimental measles. I. Pathogenesis in the normal and the immunized host. Virology 233:74–84
Mikhalap SV, Shlapatska LM, Yurchenko OV, Yurchenko M Y, Berdova GG et al (2004) The adaptor protein SH2D1A regulates signaling through CD150 (SLAM) in B cells. Blood 104:4063–4070
Mills KH (2004) Regulatory T cells: friend or foe in immunity to infection? Nat Rev Immunol 4:841–855
Minagawa H, Tanaka K, Ono N, Tatsuo H, Yanagi Y (2001) Induction of the measles virus receptor SLAM (CD150) on monocytes. J Gen Virol 82:2913–2917
Moss WJ, Ryon JJ, Monze M, Griffin DE (2002) Differential regulation of interleukin (IL)-4, IL-5, and IL-10 during measles in Zambian children. J Infect Dis 186:879–887
Mrkic B, Pavlovic J, Rulicke T, Volpe P, Buchholz CJ et al (1998) Measles virus spread and pathogenesis in genetically modified mice. J Virol 72:7420–7427
Mrkic B, Odermatt B, Klein MA, Billeter MA, Pavlovic J et al (2000) Lymphatic dissemination and comparative pathology of recombinant measles viruses in genetically modified mice. J Virol 74:1364–1372
Muller N, Avota E, Schneider-Schaulies J, Harms H, Krohne G et al (2006) Measles virus contact with T cells impedes cytoskeletal remodeling associated with spreading, polarization, and CD3 clustering. Traffic 7:849–858
Nanan R, Chittka B, Hadam M, Kreth HW (1999) Measles virus infection causes transient depletion of activated T cells from peripheral circulation. J Clin Virol 12:201–210
Naniche D, Reed SI, Oldstone MB (1999) Cell cycle arrest during measles virus infection: a G0-like block leads to suppression of retinoblastoma protein expression. J Virol 73:1894–1901
Naniche D, Yeh A, Eto D, Manchester M, Friedman RM et al (2000) Evasion of host defenses by measles virus: wild-type measles virus infection interferes with induction of alpha/beta inter-feron production. J Virol 74:7478–7484
Nejmeddine M, Barnard AL, Tanaka Y, Taylor GP, Bangham CR (2005) Human T-lymphotropic virus, type 1, tax protein triggers microtubule reorientation in the virological synapse. J Biol Chem 280:29653–29660
Niewiesk S (1999) Cotton rats ( Sigmodon hispidus ): an animal model to study the pathogenesis of measles virus infection. Immunol Lett 65:47–50
Niewiesk S, Eisenhuth I, Fooks A, Clegg JC, Schnorr JJ et al (1997) Measles virus-induced immune suppression in the cotton rat ( Sigmodon hispidus ) model depends on viral glycopro-teins. J Virol 71:7214–7219
Niewiesk S, Ohnimus H, Schnorr JJ, Gotzelmann M, Schneider-Schaulies S et al (1999) Measles virus-induced immunosuppression in cotton rats is associated with cell cycle retardation in uninfected lymphocytes. J Gen Virol 80:2023–2029
Nozawa Y, Ono N, Abe M, Sakuma H, Wakasa H (1994) An immunohistochemical study of Warthin-Finkeldey cells in measles. Pathol Int 44:442–447
Ohgimoto S, Ohgimoto K, Niewiesk S, Klagge IM, Pfeuffer J et al (2001) The haemagglutinin protein is an important determinant of measles virus tropism for dendritic cells in vitro. J Gen Virol 82:1835–1844
Ohgimoto K, Ohgimoto S, Ihara T, Mizuta H, Ishido S et al (2007) Difference in production of infectious wild-type measles and vaccine viruses in monocyte-derived dendritic cells. Virus Res 123:1–8
Ohno S, Ono N, Seki F, Takeda M, Kura S et al (2007) Measles virus infection of SLAM (CD150) knockin mice reproduces tropism and immunosuppression in human infection. J Virol 81: 1650–1659
Okada H, Kobune F, Sato TA, Kohama T, Takeuchi Y et al (2000) Extensive lymphopenia due to apoptosis of uninfected lymphocytes in acute measles patients. Arch Virol 145:905–920
Okada H, Sato TA, Katayama A, Higuchi K, Shichijo K et al (2001) Comparative analysis of host responses related to immunosuppression between measles patients and vaccine recipients with live attenuated measles vaccines. Arch Virol 146:859–874
Oldstone MB, Dales S, Tishon A, Lewicki H, Martin L (2005) A role for dual viral hits in causation of subacute sclerosing panencephalitis. J Exp Med 202:1185–1190
Ono N, Tatsuo H, Hidaka Y, Aoki T, Minagawa H et al (2001) Measles viruses on throat swabs from measles patients use signaling lymphocytic activation molecule (CDw150) but not CD46 as a cellular receptor. J Virol 75:4399–4401
Permar SR, Moss WJ, Ryon JJ, Douek DC, Monze M et al (2003) Increased thymic output during acute measles virus infection. J Virol 77:7872–7879
Pfeuffer J, Puschel K, Meulen V, Schneider-Schaulies J, Niewiesk S (2003) Extent of measles virus spread and immune suppression differentiates between wild-type and vaccine strains in the cotton rat model ( Sigmodon hispidus ). J Virol 77:150–158
Pope M, Betjes MG, Romani N, Hirmand H, Hoffman L et al (1995) Dendritic cell-T cell conjugates that migrate from normal human skin are an explosive site of infection for HIV-1. Adv Exp Med Biol 378:457–460
Ravanel K, Castelle C, Defrance T, Wild TF, Charron D et al (1997) Measles virus nucleocapsid protein binds to FcgammaRII and inhibits human B cell antibody production. J Exp Med 186:269–278
Rethi B, Gogolak P, Szatmari I, Veres A, Erdos E et al (2006) SLAM/SLAM interactions inhibit CD40-induced production of inflammatory cytokines in monocyte-derived dendritic cells. Blood 107:2821–2829
Ryon JJ, Moss WJ, Monze M, Griffin DE (2002) Functional and phenotypic changes in circulating lymphocytes from hospitalized Zambian children with measles. Clin Diagn Lab Immunol 9:994–1003
Sanchez-Lanier M, Guerin P, McLaren LC, Bankhurst AD (1988) Measles virus-induced suppression of lymphocyte proliferation. Cell Immunol 116:367–381
Sanchez-Madrid F, del Pozo MA (1999) Leukocyte polarization in cell migration and immune interactions. EMBO J 18:501–511
Schlender J, Schnorr JJ, Spielhoffer P, Cathomen T, Cattaneo R et al (1996) Interaction of measles virus glycoproteins with the surface of uninfected peripheral blood lymphocytes induces immunosuppression in vitro. Proc Natl Acad Sci U S A 93:13194–13199
Schlender J, Hornung V, Finke S, Gunthner-Biller M, Marozin S et al (2005) Inhibition of toll-like receptor 7- and 9-mediated alpha/beta interferon production in human plasmacytoid dendritic cells by respiratory syncytial virus and measles virus. J Virol 79:5507–5515
Schneider-Schaulies J, Dunster LM, Schwartz-Albiez R, Krohne G, ter Meulen V (1995) Physical association of moesin and CD46 as a receptor complex for measles virus. J Virol 69:2248– 2256
Schneider-Schaulies J, Schnorr JJ, Schlender J, Dunster LM, Schneider-Schaulies S et al (1996) Receptor (CD46) modulation and complement-mediated lysis of uninfected cells after contact with measles virus-infected cells. J Virol 70:255–263
Schneider-Schaulies J, ter Meulen V, Schneider-Schaulies S (2001) Measles virus interactions with cellular receptors: consequences for viral pathogenesis. J Neurovirol 7:391–399
Schneider-Schaulies S, Dittmer U (2006) Silencing T cells or T-cell silencing: concepts in virus-induced immunosuppression. J Gen Virol 87:1423–1438
Schneider-Schaulies S, ter Meulen V (2002) Measles virus and immunomodulation: molecular bases and perspectives. Expert Rev Mol Med 4:1–18
Schneider-Schaulies S, Kreth HW, Hofmann G, Billeter M, Ter Meulen V (1991) Expression of measles virus RNA in peripheral blood mononuclear cells of patients with measles, SSPE, and autoimmune diseases. Virology 182:703–711
Schnorr JJ, Dunster LM, Nanan R, Schneider-Schaulies J, Schneider-Schaulies S et al (1995) Measles virus-induced down-regulation of CD46 is associated with enhanced sensitivity to complement-mediated lysis of infected cells. Eur J Immunol 25:976–984
Schnorr JJ, Seufert M, Schlender J, Borst J, Johnston IC et al (1997a) Cell cycle arrest rather than apoptosis is associated with measles virus contact-mediated immunosuppression in vitro. J Gen Virol 78:3217–3226
Schnorr JJ, Xanthakos S, Keikavoussi P, Kampgen E, ter Meulen V et al (1997b) Induction of maturation of human blood dendritic cell precursors by measles virus is associated with immu-nosuppression. Proc Natl Acad Sci U S A 94:5326–5331
Servet-Delprat C, Vidalain PO, Bausinger H, Manie S, Le Deist F et al (2000) Measles virus induces abnormal differentiation of CD40 ligand-activated human dendritic cells. J Immunol 164:1753–1760
Shingai M, Inoue N, Okuno T, Okabe M, Akazawa T et al (2005) Wild-type measles virus infection in human CD46/CD150-transgenic mice: CD11c-positive dendritic cells establish systemic viral infection. J Immunol 175:3252–3261
Shingai M, Ebihara T, Begum NA, Kato A, Honma T et al (2007) Differential type I IFN-inducing abilities of wild-type versus vaccine strains of measles virus. J Immunol 179:6123–6133
Shishkova Y, Harms H, Krohne G, Avota E, Schneider-Schaulies S (2007) Immune synapses formed with measles virus-infected dendritic cells are unstable and fail to sustain T cell activation. Cell Microbiol 9:1974–1986
Shutt DC, Daniels KJ, Carolan EJ, Hill AC, Soll DR (2000) Changes in the motility, morphology, and F-actin architecture of human dendritic cells in an in vitro model of dendritic cell development. Cell Motil Cytoskeleton 46:200–221
Sidorenko SP, Clark EA (2003) The dual-function CD150 receptor subfamily: the viral attraction. Nat Immunol 4:19–24
Steineur MP, Grosjean I, Bella C, Kaiserlian D (1998) Langerhans cells are susceptible to measles virus infection and actively suppress T cell proliferation. Eur J Dermatol 8:413–420
Steinman RM (2003) The control of immunity and tolerance by dendritic cell. Pathol Biol (Paris) 51:59–60
Steinman RM, Pack M, Inaba K (1997) Dendritic cell development and maturation. Adv Exp Med Biol 417:1–6
Sun X, Burns JB, Howell JM, Fujinami RS (1998) Suppression of antigen-specific T cell proliferation by measles virus infection: role of a soluble factor in suppression. Virology 246:24–33
Tamashiro VG, Perez HH, Griffin DE (1987) Prospective study of the magnitude and duration of changes in tuberculin reactivity during uncomplicated and complicated measles. Pediatr Infect Dis J 6:451–454
Tanabe M, Kurita-Taniguchi M, Takeuchi K, Takeda M, Ayata M et al (2003) Mechanism of up-regulation of human Toll-like receptor 3 secondary to infection of measles virus-attenuated strains. Biochem Biophys Res Commun 311:39–48
Tatsuo H, Ono N, Tanaka K, Yanagi Y (2000) SLAM (CDw150) is a cellular receptor for measles virus. Nature 406(6798):893–897
tenOever BR, Servant MJ, Grandvaux N, Lin R, Hiscott J (2002) Recognition of the measles virus nucleocapsid as a mechanism of IRF-3 activation. J Virol 76:3659–3669
Valentin H, Azocar O, Horvat B, Williems R, Garrone R et al (1999) Measles virus infection induces terminal differentiation of human thymic epithelial cells. J Virol 73:2212–2221
Valsamakis A, Auwaerter PG, Rima BK, Kaneshima H, Griffin DE (1999) Altered virulence of vaccine strains of measles virus after prolonged replication in human tissue. J Virol 73:8791–8797
van Kooyk Y, Geijtenbeek TB (2003) DC-SIGN: escape mechanism for pathogens. Nat Rev Immunol 3:697–709
Vidalain PO, Azocar O, Lamouille B, Astier A, Rabourdin-Combe C et al (2000) Measles virus induces functional TRAIL production by human dendritic cells. J Virol 74:556–559
Vidalain PO, Azocar O, Rabourdin-Combe C, Servet-Delprat C (2001a) Measle virus-infected dendritic cells develop immunosuppressive and cytotoxic activities. Immunobiology 204:629–638
Vidalain PO, Azocar O, Yagita H, Rabourdin-Combe C, Servet-Delprat C (2001b) Cytotoxic activity of human dendritic cells is differentially regulated by double-stranded RNA and CD40 ligand. J Immunol 167:3765–3772
Wang N, Satoskar A, Faubion W, Howie D, Okamoto S et al (2004) The cell surface receptor SLAM controls T cell and macrophage functions. J Exp Med 199:1255–1264
Ward BJ, Griffin DE (1993) Changes in cytokine production after measles virus vaccination: predominant production of IL-4 suggests induction of a Th2 response. Clin Immunol Immunopathol 67:171–177
Weidmann A, Fischer C, Ohgimoto S, Ruth C, ter Meulen V et al (2000a) Measles virus-induced immunosuppression in vitro is independent of complex glycosylation of viral glycoproteins and of hemifusion. J Virol 74:7548–7553
Weidmann A, Maisner A, Garten W, Seufert M, ter Meulen V et al (2000b) Proteolytic cleavage of the fusion protein but not membrane fusion is required for measles virus-induced immuno-suppression in vitro. J Virol 74:1985–1993
Welstead GG, Iorio C, Draker R, Bayani J, Squire J et al (2005) Measles virus replication in lymphatic cells and organs of CD150 (SLAM) transgenic mice. Proc Natl Acad Sci U S A 102:16415–16420
Wilson NS, Villadangos JA (2005) Regulation of antigen presentation and cross-presentation in the dendritic cell network: facts, hypothesis, and immunological implications. Adv Immunol 86:241–305
Yanagi Y, Cubitt BA, Oldstone MB (1992) Measles virus inhibits mitogen-induced T cell proliferation but does not directly perturb the T cell activation process inside the cell. Virology 187:280–289
Yanagi Y, Ono N, Tatsuo H, Hashimoto K, Minagawa H (2002) Measles virus receptor SLAM (CD150). Virology 299:155–161
Yu Y, Alwine JC (2002) Human cytomegalovirus major immediate-early proteins and simian virus 40 large T antigen can inhibit apoptosis through activation of the phosphatidylinositide 3′-OH kinase pathway and the cellular kinase Akt. J Virol 76:3731–3738
Yuan H, Veldman T, Rundell K, Schlegel R (2002) Simian virus 40 small tumor antigen activates AKT and telomerase and induces anchorage-independent growth of human epithelial cells. J Virol 76:10685–10691
Zaffran Y, Destaing O, Roux A, Ory S, Nheu T et al (2001) CD46/CD3 costimulation induces morphological changes of human T cells and activation of Vav, Rac, and extracellular signal-regulated kinase mitogen-activated protein kinase. J Immunol 167:6780–6785
Zhang X, Glendening C, Linke H, Parks CL, Brooks C et al (2002) Identification and characterization of a regulatory domain on the carboxyl terminus of the measles virus nucleocapsid protein. J Virol 76:8737–8746
Zilliox MJ, Parmigiani G, Griffin DE (2006) Gene expression patterns in dendritic cells infected with measles virus compared with other pathogens. Proc Natl Acad Sci U S A 103:3363–3368
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Schneider-Schaulies, S., Schneider-Schaulies, J. (2009). Measles Virus-Induced Immunosuppression. In: Griffin, D.E., Oldstone, M.B.A. (eds) Measles. Current Topics in Microbiology and Immunology, vol 330. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-70617-5_12
Download citation
DOI: https://doi.org/10.1007/978-3-540-70617-5_12
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-70616-8
Online ISBN: 978-3-540-70617-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)