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Review

Progress towards the use of Listeria monocytogenes as a live bacterial vaccine vector for the delivery of HIV antigens

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Pages S119-S134 | Published online: 09 Jan 2014

References

  • Gallo RC, Montagnier L. The discovery of HIV as the cause of AIDS. N Engl. I Merl 349, 2283–2285 (2003).
  • Ada GL. The immunological principles of vaccination. Lancet 335, 523–526 (1990).
  • Yap KL, Ada GL, McKenzie IFC. Transfer of cytotoxic T-lymphocytes protect miceinoculated with influenza virus. Nature 273, 238–240 (1978).
  • Raychaudhuri S, Rock KL. Fully mobilizing host defense, building better vaccines.Nature Biotech. 16, 1025–1031(1998).
  • Levy JA. Pathogenesis of human immunodeficiency virus infection. Microbial. Rev. 57, 183–289 (1993).
  • Kou RA, Safrit JT, Cao Y et al Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus Type 1 syndrome.' Vim]: 68, 4650–4655 (1994).
  • Pantaleo G, Demarest JF, Schacker T et al The qualitative nature of the primary immune response to HIV infection is a prognosticator of disease progression independent of the initial level of plasma viremia. Proc. Natl Acad Sc]. USA 94, 254–258 (1997).
  • Ogg GS, Jin X, Bonhoeffer S et al. Quantitation of HIV-1-specific cytotoxic lymphocytes and plasma load of viral RNA. Science 279, 2103–2106 (1998).
  • Rowland-Jones SL, Tan R, McMichael A. Role of cellular immunity in protection against HIV infection. Adv. Immunol 65, 277–346 (1997).
  • Kaul R, Plummer FA, Kiman, J et al. HIV- 1-specific mucosal CD8+ lymphocyte responses in the cervix of HIV-1-resistant prostitutes in Nairobi. J: Immunol 164, 1602–1611 (2000).
  • Goulder P, Price, D, Nowak M, Rowland- Jones SL, Phillips R, McMichael A. Co-evolution of human immunodeficiency virus and cytotoxic T-lymphocyte responses. hnmunol. Rev 159, 17–29 (1997).
  • Price DA, Klenerman P, Booth BL, Phillips RE, Sewell AK. Cytotoxic T-lymphocytes, chemokines and antiviral immunity. Immunol Today20, 212–216 (1999).
  • Borrow P, Lewicki H, Wei X et al. Antiviral pressure exerted by HIV-1-specific cytotoxic T-lymphocytes (CTLs) during primary infection demonstrated by rapid selection of CTL escape virus. Nature Merl 3, 205–211 (1997).
  • Rowland-Jones SL, Dong T, Karusa P et al The role of cytotoxic T-cells in HIV infection. Dev. Biol. Stand. 92, 209–214 (1998).
  • Rowland-Jones SL, Dong T, Fowka KR et al. Cytotoxic T-cell responses to multiple conserved HIV epitopes in HIV-resistant prostitutes in Nairobi. j Clin. Invest. 102, 1758–1765 (1998).
  • Paul WE. Reexamining AIDS research priorities. Science 267,633–636 (1995).
  • Weiskirch LM, Paterson Y. Listeria monocytogenes a potent vaccine vector for neoplastic and infectious disease. Immunol Rev 158,159–169 (1997).
  • Gunn GR, Zubair A, Paterson Y. Harnessing bacteria for cancer immunotherapy. In: Vaccines: Delivery Systems. Goebel W, Dietrich G (Eds), Horizon Scientific Press, USA, Chapter 14, 315–348 (2002).
  • Weiskirch LM, Paterson Y. The use of Listeria monocytogenes recombinants as vaccine vectors in infectious and neoplastic disease. In: !!!!!!Intracellular Bacterial Vaccine Vectors: Paterson Y (Ed.), John Wiley & Sons, Inc., NY, USA, Chapter 7,223–259 (1999).
  • Jensen ER, Shen H, Wettstein FO, Ahmed R, Miller JF. Recombinant Listeria monocytogenes as a live vaccine vehicle and a probe for studying cell-mediated immunity. Immunol. Rev 158, 147–157 (1997).
  • Cooper J, Walker RD. Listeriosis. Vet. Clin. North Am. Foocl Anim. Bart. 14,113–125 (1998).
  • Portnoy DA, Chakraborty T, Goebel W, Cossart P. Molecular determinants of Listeria monocytogenes pathogenesis. Infect. Immun. 60,1263–1267 (1992).
  • Crocker PR, Milon G. Macrophages in control of haematopoiesis. In: The Natural Immune System Pail II the 11/Lcmphage. Lewis CE, OD McGhee J (Eds), Oxford University Press, Oxford, UK, 115–156 (1992).
  • Havell EA, Beretich GR, Carter PB. The mucosal phase of Listeria infection. Immunobiology201, 164–177 (1999).
  • Lecuit M, Vandormael-Pourin S, Lefort J et al. A trangenic model for Listeriosis: Role of internalin in crossing the intestinal barrier. Science 292,1722–1725 (2001).
  • ••Explained why mice are a poor model forexamining human listerial infection by the oral route. The mouse E-cadherin molecule differs from the human and guinea-pig E-cadherin in important amino acid residues that bind to the listerial invasion protein in1A.
  • Braun L, Cossart P. Interactions between Listeria monocytogenes and host mammalian cells. Ifrlicrob. Infect. 2, 803–811 (2000).
  • Shen Y, Naujokas M, Park M, Ireton K. InIB-dependent internalization of Listeria is mediated by the Met receptor tyrosine kinase. Ce11103, 501–510 (2000).
  • Mackaness GB. Cellular resistance to infection. Exp. Med 116,381–390 (1962).
  • Edelson BT, Cossart P, Unanue ER. Cutting Edge: Paradigm revisited: antibody provides resistance to Listeria infection. Immunol 163,4087–4090 (1999).
  • Edelson BT, Unanue ER. Intracellular antibody neutralizes Listeria growth. Immunity 14,503–512 (2001).
  • Manohar M, Baumann DO, Bos NA, Cebra JJ. Gut colonization of mice with actA-negative mutant of Listeria monocytogenes can stimulate a humoral mucosal immune response. Infect. Immun. 69,3542–3549 (2001).
  • Vijh S, Pamer EG. Cell Biology and immune response to Listeria monocytogenes, an intracellular pathogen. In Intraceliular Bacterial Vaccine Vectors. Immunology, Cell Biology and Genetics. Paterson Y (Ed.), John Wiley & Sons Inc., NY, USA, Chapter 4 111–147 (1999).
  • Kaufmann SH. Immunity to intracellular bacteria. Ann. Rev. Immunol 11,129–163 (1993).
  • Ladel CH, Flesh IEF, Arnoldi J, Kaufman SHE. Studies with MHC-deficient knockout mice reveal impact of both MHC I- and MHC-II-dependent T-cell responses on Listeria monocytogenes infection. Immunol 153,3116–3122 (1994).
  • Harty JT, Bevan MJ. Specific immunity to Listeria monocytogenesin the absence of IFN-y. Immunity3, 109–117 (1995).
  • Badovinac VP, Harty JT. Adaptive immunity and enhanced CD8* T-cell response to Listeria monocytogenes in the absence of perforin and IFN-y. I Immunol 164,6444–6452(2000).
  • Barry RA, Archie Bouwer HG, Clark TR, Cornell KA, Hinrichs DJ. Protection of interferon-y knockout mice against Listeria monocytogenes challenge following intramuscular immunization with DNA vaccines encoding listeriolysin 0. Vaccine 21,2122–2132 (2003).
  • Schafer R, Portnoy DA, Brassell SA, Paterson Y. Induction of a cellular immune response to a foreign antigen by a recombinant Listeria monocytogenes vaccine. Immunol 149,53–59 (1992).
  • Ikonomidis G, Paterson Y, Kos F, Portnoy D. Delivery of a viral antigen to the class I processing and presentation pathway by L. monocytogenes. I Exp. Med. 180, 2209–2218 (1994).
  • Shen H, Slifka MK, Matloubian M, Jensen ER, Ahmed R, Miller JE Recombinant Listeria monocytogenes as a live vaccine vehicle for the induction of protective antiviral cell-mediated immunity. Proc. Nat! Acad. Sci. USA 92,3987–3991 (1995).
  • Gunn GR, Zubair A, Peters CH, Pan ZK, Wu TC, Paterson Y. Two L. monocytogenes vaccine vectors that express different molecular forms of HPV-16 E7 induce qualitatively different T-cell immunity that correlates with their ability to induce regression of established tumors immortalized by HPV-16. I Immunol 167, 6471–6479 (2001).
  • •First study to evaluate L. monocytogenes as a vector for a relevant human tumor-associated antigen. The authors show that a highly attenuated Listeria construct, that is cleared in SCID mice, can induce the regression of established HPV immortalized tumors in syngeneic mice.
  • Sewell, DA, Douven D, Pan ZK, Rodriguez A, Paterson Y. Regression of HPV-positive tumors treated with a new Listeria monocytogenes vaccine. Arch. Otorhinolaryngrol 130,92–97 (2004).
  • Mata M, Yao ZJ, Zubair A, Syres K, Paterson Y. Evaluation of a recombinant L. monocytogenes expressing an HIV protein that protects mice against viral challenge. Vaccine 19,1435–1445 (2001).
  • •These investigators show that immunization with a Listeria monocytogenes that expresses HIV-1 Gag can protect mice against challenge with vaccinia that expresses HIV-1 Gag.
  • Dietrich G, Bubert A, Gentschev I et al Delivery of antigen-encoding plasmid DNA into the cytosol of macrophages by attenuated suicide Listeria monocytogenes. Nature Biotech. 16,181–186 (1998).
  • Pilgrim S, Stritzker J, Schoen C et al Bactofection of mammalian cells by Listeria monocytogenes improvement and mechanism of DNA delivery. Gene Ther. 10,2036–2045 (2003).
  • Goossens PL, Milon G, Cossart P, Saron ME. Attenuated Listeria monocytogenes as a live vector for induction of CD8* T-cells in vivz a study with the nucleoprotein of the lymphocytic choriomeningitis virus. Int. Immunol 7,797–805 (1995).
  • Ikonomidis G, Portnoy DA, Gerhard W Paterson Y. Influenza-specific immunity induced by recombinant Listeria monocytogenes vaccines. Vaccine 15, 433–440 (1997).
  • Soussi N, Milon G, Colle JH, Mougneau E, Glaichenhaus N, Goossens PL. Listeria monocytogenes as a short-lived delivery system for the induction of Type 1 cell-mediated immunity against the p36/LACK antigen of Leishmania major Infect. IMMUIL 68,1498–1506 (2000).
  • Mata M, Paterson Y. Thl T-cell responses to HIV-1 Gag protein delivered by a Listeria monocytogenesvaccine are similar to those induced by endogenous listerial antigens. hnmunol 163,1449–1459 (1999).
  • Soussi N, Saklani-Jusforgues H, Colle JH, Milon G, Glaichenhaus N, Goossens PL. Effect of intragastric and ip. immunisation with attenuated and wild type LACK-expressing Listeria monocytogenes on control of murine Leishmania major infection. Vaccine 20,2702–2712 (2002).
  • •The ability of Listeria to provide protective immunity against leishmaniasis in the susceptible BALB/c mouse is established and shown to be due to its propensity to induce strong T-helper (Th)1 responses.
  • Saklani-Jusforgues H, Fontan E, Soussi N, Milon G, Goossens PL. Enteral immunization with attenuated recombinant Listeria monocytogenes as a live vaccine vector: organ-dependent dynamics of CD4 T-lymphocytes reactive to a Leishmania mqjortracer epitope. Infect. Immun. 71,1083-1090 (2003).
  • Pan ZK, Ikonomidis G, I a7enby A, Pardoll D, Paterson Y. A recombinant Listeria monocytogenes vaccine expressing a model tumour antigen protects mice against lethal tumour cell challenge and causes regression of established tumours. Nature Med. 1, 471–477 (1995).
  • Pan ZK, Ikonomidis G, Pardoll D, Paterson Y. Regression of established tumors in mice mediated by the oral administration of a recombinant Listeria monocytogenes vaccine. Cancer Res. 55,4776–4779 (1995).
  • Pan ZK, Weiskirch LM, Paterson Y. Regression of established B16F10 melanoma with a recombinant Listeria monocytogenes vaccine. Cancer Res. 59, 5264–5269 (1999).
  • Paglia P, Arioli I, Frahm N, Chakraborty T, Colombo MP, Guzman C. The defined attenuated Listeria monocytogenes delta mpl2 mutant is an effective oral vaccine carrier to trigger a long-lasting immune response against a mouse fibrosarcoma. Eur. Immunol 27,1570–1575 (1997).
  • Peng X, Hussain SF, Paterson Y. The upregulation of cytokine secretion and co-stimulatory molecules on dendritic cells infected with two Iisteria monocytogenes vaccines targeting HPV-16 E7 correlates with their ability to induce an antitumor response. Immunol 172,6030–6038 (2004).
  • Jensen ER, Selvakumar R, Shen H, Ahmed R, Wettstein FO, Miller JF. Recombinant Listeria monocytogenes vaccination eliminates papillomavirus-induced tumors and prevents papilloma formation from viral DNA. j Viral 71, 8467–8474 (1997).
  • Liau LM, Jensen ER, Kremen TJ et al Tumor immunity within the central nervous system stimulated by recombinant Listeria monocytogenes vaccination. Cancer Res. 15,2287–2293 (2002).
  • Frankel FR, Hegde S, Lieberman J, Paterson Y. Induction of cell-mediated immune responses to human immunodefiency virus Type 1 Gag protein by using Listeria monocytogenes as a live vaccine vector. j Immund 155, 4775–4782 (1995).
  • Mata M, Travers P, Liu Q, Frankel FR, Paterson Y. The MHC class I restricted immune response to HIV-GAG in BALB/c mice selects an epitope which does not have a predictable MHC binding motif and binds to Kd through interactions between a glutamine at P3 and pocket D. j Immunol 161, 2985–2993 (1998).
  • Klein MR, van Baalen CA, Holwerda AM et al Kinetics of Gag-specific cytotoxic T-lymphocyte responses during the clinical course of HIV-1 infection: a longitudinal analysis of rapid progressors and long-term asymptomatics. j Exp. Med. 181, 1365–1372 (1995).
  • Jones DE, Elloso MM, Scott P. Host susceptibility factors to cutaneous leishmaniasis. Front Eiosci. 3, D1171—D1180 (1998).
  • Friedman RS, Frankel FR, Xu Z, Lieberman J. Induction of human immunodeficiency virus (HIV)-specific CD8 T-cell responses by Listeria monocytogenes and a hyperattenuated Listeria strain engineered to express HIV antigens. j Viral 74,9987–9993 (2000).
  • Thompson, RJ, Bouwer HG, Portnoy DA, Frankel FR. Pathogenicity and immunogenicity of a Listeria monocytogenes strain that requires D-alanine for growth. Infect. Immun. 66,3552–3561 (1998).
  • Guzman CA, Saverino D, Medina E. Attenuated Listeria monocytogenes carrier strains can deliver an HIV-1 gp120 T-helper epitope to MHC class II-restricted human CD4* T-cells. Eur j Immunol 28, 1807–1814 (1998).
  • Ogra PL, Faden H, Welliver RC. Vaccination strategies for mucosal immune responses. Clin. Mcrobiol Revs. 14, 430–445 (2001).
  • Rayevskaya MV, Frankel FR. Systemic immunity and mucosal immunity are induced against human immunodeficiency virus Gag protein in mice by a new hyperattenuated strain of Listeria monocytogenes. j Viral. 75,2786–2791 (2001).
  • Rayevskaya M, Kushnir N, Frankel FR. Safety and immunogenicity in neonatal mice of a hyperattenuated Listeria vaccine directed against human immunodeficiency virus.j Viral 76,918–22 (2002).
  • •These investigators show that it is possible to suitably attenuate Listeria so that it is safe to use as a vaccine with neonatal animals.
  • Snyder SH, Kim PM. D-amino acids as Putative neurotransmitters: focus on D-serine. Neurochem. Res. 25,553–560 (2000).
  • Peters C, Peng X, Douven D, Pan ZK, Paterson Y. The induction of HIV Gag specific CD8+ T-cells in the spleen and gut-associated lymphoid tissue by parenteral or mucosal immunization with recombinant Listeria monocytogenes HIV Gag. Immund 170,5176–5187 (2003).
  • ••Reports a systematic analysis of CD8+ T-cell responses to HIV-1 Gag delivered by Listeria to the BALM mouse. Intrarectal, intraperitoneal and oral immunization routes were compared for their ability to induce Gag-specific CD8+ T-cells in the spleen, LP PP and MLN.
  • Novembre FJ, Saucier M, Anderson DC. Development of AIDS in a chimpanzee infected with human immunodeficiency virus Type 1.1 Vim' 71,4086–4091 (1991).
  • Hirsch V M, Johnson PR. Pathogenic diversity of simian immunodeficiency viruses. Virus Res. 32,183–203 (1994).
  • Letvin NL, King NW. Immunological and pathologic manifestations of the infection of rhesus monkeys with simian immunodeficiency virus of macaques. Acquir Immune Defic. Sync/. 3,1023–1040 (1990).
  • Anderson DC, McClure HM. Listeriosis in Nonhuman Primates I Jones TC, Mohr Hunt, U. RD (Eds), Springer-Verlag, Berlin, Germany and NY, USA, 135–141 (1993).
  • Chalifoux LV, Hajema EM. Septicemia and meningoencephalitis caused by L monocytogenesin a neonatal Micaca fasciluaris. Med Primatol 10,336–339 (1981).
  • McClure HM, Brodie AR, Anderson DC, Swenson RB. Bacterial infections of non-human primates. In Primates: the Road to Self-sustaining Populations. Benirschke K (Ed.). Springer, Berlin, Germany & NY, USA, 531–556 (1986).
  • Boyer JD, Robinson TM, Maciag PC et al DNA prime listeria boost induces a cellular immune response to SW antigens in the rhesus macaque model that is apable of suppressing SIV239 viral replication. (Manuscript submitted).
  • ••First paper to explore the ability of Listeriato induce immune responses in nonhuman primates. It shows that a prime—boost vaccine regimen using DNA priming and Listeria boosting conveys a protective advantage against SIV239 challenge. It also shows that Listeria can be administered safely to nonhuman primates.
  • Gellin BG, Broome CV Listeriosis. JAIVIA 261,1313–1320 (1989).
  • Lorber B. Listeriosis. Clin. Infect. Dis. 24, 1–11 (1997).
  • Cabanes D, Dehoux P, Dussurget O, Frangeul L, Cossart P. Surface proteins and the pathogenic potential of L. monocytogenes. Tends Mcrobiol 10, 238–245 (2002).
  • Peters C, Domann E, Darbouche A, Chakraborty T, Mielke ME. Tailoring host immune responses to Listeria by manipulation of virulence genes — the interface between innate and acquired immunity FEMS Immunol Med. Mcmbiol. 35,243–253 (2003).
  • ••A thorough comparison of attenuated Listeria strains for their safety and imrnunogenicity.
  • Angelakopoulos H, Loock K, Sisul DM, Jensen ER, Miller JF, Hohmann EL, Safety and shedding of an attenuated strain of Listeria monocytogenes with a deletion of actA/plcB in adult volunteers: a dose escalation study of oral inoculation. Infect. Immun. 70,3592–3601 (2002).
  • ••First safety test in humans (volunteers) of an attenuated Listeria strain that could be a useful vaccine carrier. Little toxicity was associated with the vaccine.
  • Hone DM, Shata MT, Pascual DW, Lewis GK. Mucosal vaccination with Salmonella vaccine vectors. In: Inbacellular Bacterial Vaccine Vectors Paterson Y (Ed.), John Wikeyv & Sons Inc, NY, USA 171–222 (1999).
  • Autret N, Dubail I, Trieu-Cuot P, Berche P, Charbit A. Identification of new genes involved in the virulence of Listeria monocytogenes by signature-tagged transposon mutagenesis. Infect. Immun. 69, 2054–2065 (2001).
  • Sciali AR, Rarick TL. Salmonella sepsis and second trimester pregnancy loss. Obstet. Cynecol 79,820–821 (1992).
  • Vugia D, Hadler J, Blake P et al Preliminary FoodNet data on the incidence of foodborne illness — selected sites, United States, 2001. MMWR Morb. Mortal. Wkly. Rep. 51,325-329 (2002).
  • Young D, Hussell T, Dougan G. Chronic bacterial infections: living with unwanted guests. Nature Immunol 3,1026–1032 (2002).
  • Netea MG, Radstake T, Joosten LA. Salmonella septicemia in rheumatoid arthritis patients receiving antiTNF therapy: association with decreased interferon-y production and Toll-like receptor 4 expression. Arthritis Rheum. 48, 1853–1857 (2003).
  • Farber JM, Peterkin PI. Listeria monocytogenes, a food-borne pathogen.Microbial. Revs. 55,476–511 (1991).
  • Dalton CB, Austin CC, Sobel J et al An outbreak of gastroenteritis and fever due to Listeria monocytogenesin milk. N Engl. J. Med. 336,100–105 (1997).
  • Blaser MJ, Newman L. A review of human salmonellosis: I. Infective dose. Rev Infect. Dis. 4,1096–1106 (1982).
  • Altare F, Lammas D, Revy, P et al Inherited interleukin-12 deficiency in a child with Bacille Calmette-Guerin and Salmonella enteriditis disseminated infection. J. Gun. Invest. 102,2035-2040 (1998).
  • Snider DE. Ethical issues in tuberculosis vaccine trials. Clin. Infect. Dis. 30, S271—S275 (2000).
  • Antaya RJ, Gardner, ES, Bettencourt, MS et al Cutaneous complications of BCG vaccination in infants with immune disorders: two cases and a review of the literature. Fed. Derm. 18,205–209 (2001).
  • Sumida SM, Truitt DM, Kishko MG et al Neutralizing antibodies and CD8+ T-lymphocytes both contribute to immunity to adenovirus serotype 5 vaccine vectors. J. Viral. 78,2666-2673 (2004).
  • Bouwer HG, Shen H, Fan X et al Existing antilisterial immunity does not inhibit the development of a Listeria monocytogenes-specific primary cytotoxic T-lymphocyte response. Infect Immun. 67,253–258 (1999).
  • ••Demonstrates that prior exposure to mutant strains of L. monocytogenes that lack certain immunodominant epitopes does not inhibit the development of a primary cu, response to these epitopes delivered by wild-type L. monocytogenes These results suggest that pre-existing vector immunity will not inhibit the use of L. monocytogenes as a vaccine vector.

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