90 research outputs found
Trypanosoma cruzi : measurement of DNA quantity in different isoenzymic strains : inferences on the ploidy of these strains
Sera from Trypanosoma b. gambiense infected patients cross-react with a Trypanosoma cruzi recombinant protein
In previous studies, we and others have shown utility of a 24-kDa #Trypanosoma cruzi recombinant antigen (rTc24) for serological diagnosis of Chagas' disease. Also, this molecule has been proved useful to evaluate cure of chagasic patients who submit to specific treatment. However, in all the studies done so far, the 24-kDa protein was used as a fusion with a Gluthatione-S-transferase (GST) of #Schistosoma japonicum, therefore, parallel assays to determine the anti-GST responses of all sera were required to deduce the GST noise in serological tests. Here, we show the subcloning by polymerase chain reaction of the cDNA encoding the #T. cruzi$ 24-kDa antigen in a vector system (pQE) allowing us to obtain Tc24 recombinant protein as a single molecule. The highly reactivity of chagasic sera from Colombia, Ecuador, Brazil and Bolivia in ELISA against the recombinant antigen is confirmed. However, sera from patients infected with African trypanosomes recognize rTc24 in ELISA and blot. The relevance of these findings in the context of Chagas' disease diagnosis and/or the relationship with African trypanosomes is analyzed. (Résumé d'auteur
Results of vaccination against canine visceral leishmaniasis (Leishmania infantum) in enzootic areas
Protection against canine leishmaniasis was evaluated in dogs living in enzootic areas in the south of
France, and vaccinated with a candidate vaccine, LiESP with the adjuvant MDP. A double-blind field
study was carried out in a large number of dogs (n = 414) over two years. At the end of the study, infection
rate was 0% in vaccinated dogs versus 5.14% in the placebo group. The candidate vaccine induced
an effective and lasting immunity against canine leishmaniasis.La protection contre la
leishmaniose canine est évaluée chez des chiens vivant en zone d'enzootie dans le sud de la
France, vaccinés par un candidat LiESP adjuvé par MDP. Une étude de terrain randomisée en
double aveugle est conduite dans une large population de chiens (n = 414), durant une
période de deux années. À l'issue de l'étude, le taux d'infection est de 0 % chez les chiens
vaccinés et de 5,14 % chez les chiens du groupe placebo. Le candidat vaccinal a induit une
immunité efficace, durable contre la leishmaniose canine
Circulating antibodies directed against tryptophan-like epitopes in sera of patients with human African trypanosomiasis
Canine leishmaniosis due to Leishmania infantum: immunotherapy trials
As most methods currently available to treat and control canine leishmaniasis have a limited efficacy,
researchers are testing immunotherapeutic methods with great interest. Excreted–secreted antigens
(ES Ag) of promastigotes of Leishmania infantum cultured in a defined medium were selected.
Three Leishmania–infected dogs received two intradermal injections of 25 mg of ES Ag, at 3 weeks
interval. This treatment was the first ever in one of the dogs, whereas the other two had previously
received a standard treatment with Glucantime® and Zyloric®. Marked clinical improvement was noted
as of Day 15 after the first injection, as well as an intense leishmanicide activity in collected monocytes,
and a significant decrease of antibody titres. No clinical relapse was recorded over two years later.La plupart des méthodes
disponibles aujourd'hui de traitement et de contrĂ´le de la leishmaniose canine sont d'une
efficacité limitée, aussi le développement de méthodes immunothérapeutiques est-il d'un
grand intérêt. Des antigènes d'excrétion-sécrétion (Ag ES) de promastigotes de Leishmania
infantum cultivés en milieu défini sont retenus. Trois chiens leishmaniens en reçoivent 25
μg, 2 fois à 3 semaines d'intervalle, par la voie intra-dermique: un chien est traité pour
la première fois selon ce protocole, les 2 autres avaient été traités antérieurement selon
un protocole classique à base de glucantime et de zyloric. Une nette amélioration clinique
est observée dès J15 après la première injection, ainsi qu'une forte activité leishmanicide
des monocytes récoltés et une diminution significative des titres en anticorps. Aucune
rechute clinique n'est enregistrée plus de 2 ans plus tard
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