25 research outputs found

    Potentiating Effects of MPL on DSPC Bearing Cationic Liposomes Promote Recombinant GP63 Vaccine Efficacy: High Immunogenicity and Protection

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    Visceral leishmaniasis (VL), a vector-transmitted disease caused by Leishmania donovani, is potentially fatal if left untreated. Vaccination against VL has received limited attention compared with cutaneous leishmaniasis, although the need for an effective vaccine is pressing for the control of the disease. Earlier, we observed protective efficacy using leishmanial antigen (Ag) in the presence of either cationic liposomes or monophosphoryl lipid A-trehalose dicorynomycolate (MPL-TDM) against experimental VL through the intraperitoneal (i.p.) route of administration in the mouse model. However, this route of immunization is not adequate for human use. For this work, we developed vaccine formulations combining cationic liposomes with MPL-TDM using recombinant GP63 (rGP63) as protein Ag through the clinically relevant subcutaneous (s.c.) route. Two s.c. injections with rGP63 in association with cationic liposomes and MPL-TDM showed enhanced immune responses that further resulted in high protective levels against VL in the mouse model. This validates the combined use of MPL-TDM as an immunopotentiator and liposomes as a suitable vaccine delivery system

    Conference Highlights of the 16th International Conference on Human Retrovirology: HTLV and Related Retroviruses, 26–30 June 2013, Montreal, Canada

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    Possibilities and challenges for developing a successful vaccine for leishmaniasis

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    Pomacea canaliculata (Mollusca, Gastropoda) in Patagonia: potential role of climatic change in its dispersion and settlement

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    Pomacea canaliculata (Lamarck, 1822) (Mollusca Gastropoda) shows a large native distribution range in South America, reaching as far south as 37Âș S (Buenos Aires, Argentina). This species was deliberately introduced into Southeast Asia around 1980 and subsequently underwent a rapid intentional or accidental dispersal into many countries in the region. It was also introduced into North and Central America and Hawaii. In this contribution we record the presence of P. canaliculata in Patagonia, assessing the possible influence of climatic change in the new establishment of this species there. Three samplings (between September 2004 and April 2005) were carried out at 38Âș 58' 20.2" S-68Âș 11' 27.3" W. In the sampling we found two adult specimens of P. canaliculata and numerous egg clutches. Pomacea canaliculata is naturally distributed in the Plata and Amazon Basins. The southern boundary of this species has been established as the isotherms of 14 ÂșC and 16 ÂșC in Buenos Aires province, and precipitations of 900 to 600 mm/year. This study also analysed variations in annual temperature and precipitation in Patagonia. Average temperatures show an increase over the years, although not constantly. Important modifications in precipitation regime in northern Patagonia, triggered by global climatic changes, could be beneficial for the settlement of populations of P. canaliculata in this new area, where precipitation increased enough to reach values similar to those in the southernmost area of distribution of this species

    Virulence factors of the Mycobacterium tuberculosis

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    The Mycobacterium tuberculosis complex (MTBC) consists of closely related species that cause tuberculosis in both humans and animals. This illness, still today, remains to be one of the leading causes of morbidity and mortality throughout the world. The mycobacteria enter the host by air, and, once in the lungs, are phagocytated by macrophages. This may lead to the rapid elimination of the bacillus or to the triggering of an active tuberculosis infection. A large number of different virulence factors have evolved in MTBC members as a response to the host immune reaction. The aim of this review is to describe the bacterial genes/proteins that are essential for the virulence of MTBC species, and that have been demonstrated in an in vivo model of infection. Knowledge of MTBC virulence factors is essential for the development of new vaccines and drugs to help manage the disease toward an increasingly more tuberculosis-free world
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