Efficacy of a trans-sialidase-ISCOMATRIX subunit vaccine candidate to protect against experimental Chagas disease

被引:36
|
作者
Bontempi, Ivan Alejandro [1 ]
Vicco, Miguel Hernan [1 ]
Cabrera, Gabriel [1 ]
Villar, Silvina Raquel [2 ,3 ]
Gonzalez, Florencia Belen [2 ,3 ]
Roggero, Eduardo Angel [2 ,3 ]
Ameloot, Paul [4 ,5 ]
Callewaert, Nico [4 ,5 ]
Perez, Ana Rosa [2 ,3 ]
Marcipar, Ivan Sergio [1 ]
机构
[1] Univ Nacl Litoral, Fac Bioquim & Ciencias Biol, Santa Fe, Argentina
[2] Univ Nacl Rosario, Fac Ciencias Med, IDICER CONICET, RA-2000 Rosario, Santa Fe, Argentina
[3] Univ Nacl Rosario, Fac Ciencias Med, Inst Inmunol, RA-2000 Rosario, Santa Fe, Argentina
[4] Univ Ghent VIB, Inflammat Res Ctr, Med Biotechnol Unit, Ghent, Belgium
[5] Univ Ghent, Dept Biochem & Microbiol, B-9000 Ghent, Belgium
关键词
Trypanosoma cruzi; ISCOM; Trans-sialidase; Vaccine; TRYPANOSOMA-CRUZI INFECTION; IFN-GAMMA; T-CELLS; IMMUNITY; IMMUNIZATION; ADJUVANTS; ANTIGENS; MICE; PATHOGENESIS; MACROPHAGES;
D O I
10.1016/j.vaccine.2015.01.044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recombinant protein vaccines are safe but elicit low immunological responses. The new generation of adjuvants is currently reversing this situation. Here, a new antigen-adjuvant combination for protection against experimental Chagas disease was assessed. The antigen used in the formulation was a glycosylated mutant inactive trans-sialidase (mTS) that was previously proven to be highly protective against Trypanosoma cruzi infection; here, we show that it can be produced in large quantities and high quality using Pichia pastoris. The adjuvant used in the formulation was ISCOMATRIX (IMX), which was found to be effective and safe in human clinical trials of vaccines designed to control other intracellular infections. Fifteen days after the third immunization, mice immunized with mTS-IMX showed a TS-specific IgG response with titers >10(6) and high avidity, an increased IgG(2)a/IgG1 ratio, significant delayed-type hypersensitivity (DTH) reactivity, a balanced production of IFN-gamma and IL-10 by splenocytes and a strong IFN-gamma secretion by CD8(+) T lymphocytes. When these mice where challenged with 1000 trypomastigotes of T. cruzi, all mTS-IMX immunized mice survived, whereas mice immunized with mTS alone, IMX or PBS exhibited high mortality. Remarkably, during acute infection, when the parasitemia is highest in this infection model (day 21), mTS-IMX immunized mice had similar to 50 times less parasitemia than non-immunized mice. At this moment and also in the chronic phase, 100 days after infection, tissue presented similar to 4.5 times lower parasite load and associated inflammatory infiltrate and lesions. These results indicate that protection against Chagas disease can be achieved by a protein antigen-adjuvant mTS formulation that is compatible with human medicine. Therefore, the current formulation is a highly promising T. cruzi vaccine candidate to be tested in clinical trials. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1274 / 1283
页数:10
相关论文
共 36 条
  • [1] Immunogenicity and efficacy of a subunit therapeutic vaccine against Chagas disease
    Jones, K. M.
    Respress, J. L.
    Barry, M. A.
    Keegan, B. P.
    Beaumier, C. M.
    Pollet, J.
    Zhan, B.
    Kendricks, A. L.
    Yoshida, N.
    Feng, L.
    Bottazzi, M. E.
    Hotez, P. J.
    TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2015, 20 : 52 - 52
  • [2] Trypanosoma cruzi trans-Sialidase as a Potential Vaccine Target Against Chagas Disease
    da Costa, Kelli Monteiro
    Marques da Fonseca, Leonardo
    dos Reis, Jhenifer Santos
    Santos, Marcos Andre Rodrigues da Costa
    Previato, Jose Osvaldo
    Mendonca-Previato, Lucia
    Freire-de-Lima, Leonardo
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2021, 11
  • [3] Trans-sialidase overcomes many antigens to be used as a vaccine candidate against Trypanosoma cruzi
    Bontempi, Ivan
    Fleitas, Pedro
    Poato, Alexia
    Vicco, Miguel
    Rodeles, Luz
    Prochetto, Estefania
    Cabrera, Gabriel
    Beluzzo, Bruno
    Arias, Diego
    Racca, Andrea
    Guerrero, Sergio
    Marcipar, Ivan
    IMMUNOTHERAPY, 2017, 9 (07) : 555 - 565
  • [4] Trypanosoma cruzi trans-sialidase as a drug target against Chagas disease (American trypanosomiasis)
    Miller, Bill R., III
    Roitberg, Adrian E.
    FUTURE MEDICINAL CHEMISTRY, 2013, 5 (15) : 1889 - 1900
  • [5] Intranasal Trans-Sialidase Vaccine Mitigates Acute and Chronic Pathology in a Preclinical Oral Chagas Disease Model
    Pacini, Maria Florencia
    Bulfoni Balbi, Camila
    Dinatale, Brenda
    Farre, Cecilia
    Cacik, Paula
    Gonzalez, Florencia Belen
    Marcipar, Ivan
    Perez, Ana Rosa
    VACCINES, 2024, 12 (10)
  • [6] FAILURE OF A SUBUNIT BOVINE HERPESVIRUS-1 VACCINE TO PROTECT AGAINST EXPERIMENTAL RESPIRATORY-DISEASE IN CALVES
    DARCEL, CL
    JERICHO, KWF
    CANADIAN JOURNAL OF COMPARATIVE MEDICINE-REVUE CANADIENNE DE MEDECINE COMPAREE, 1981, 45 (01): : 87 - 91
  • [7] Core Proteomics and Immunoinformatic Approaches to Design a Multiepitope Reverse Vaccine Candidate against Chagas Disease
    Islam, Sk Injamamul
    Sanjida, Saloa
    Ahmed, Sheikh Sunzid
    Almehmadi, Mazen
    Allahyani, Mamdouh
    Aljuaid, Abdulelah
    Alsaiari, Ahad Amer
    Halawi, Mustafa
    VACCINES, 2022, 10 (10)
  • [8] Evaluation in mice of the immunogenicity and protective efficacy of a tetravalent subunit vaccine candidate against dengue virus
    Lazo, Laura
    Izquierdo, Alienys
    Suzarte, Edith
    Gil, Lazaro
    Valdes, Iris
    Marcos, Ernesto
    Alvarez, Mayling
    Romero, Yaremis
    Guadalupe Guzman, Maria
    Guillen, Gerardo
    Hermida Cruz, Lisset
    MICROBIOLOGY AND IMMUNOLOGY, 2014, 58 (04) : 219 - 226
  • [9] Examination of the immunogenicity of experimental subunit vaccine against Newcastle Disease virus
    Milic, N
    GadanskiOmerovic, G
    Asanin, R
    Markovic, B
    Palic, T
    Simonovic, L
    Rasic, Z
    Krnjaic, D
    Crvak, B
    Milisavljevic, S
    ACTA VETERINARIA-BEOGRAD, 1996, 46 (5-6): : 307 - 315
  • [10] Immunization with an engineered mutant trans-sialidase highly protects mice from experimental Tryponosoma cruzi infection:: A vaccine candidate
    Fontanella, German H.
    De Vusser, Kristof
    Laroy, Wouter
    Daurelio, Lucas
    Nocito, Ana Lia
    Revelli, Silvia
    Contreras, Roland
    VACCINE, 2008, 26 (19) : 2322 - 2334