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1.
J Immunol ; 193(6): 2961-70, 2014 Sep 15.
Article in English | MEDLINE | ID: mdl-25098291

ABSTRACT

Leishmania (Viannia) parasites are etiological agents of cutaneous leishmaniasis in the New World. Infection is characterized by a mixed Th1/Th2 inflammatory response, which contributes to disease pathology. However, the role of regulatory T cells (Tregs) in Leishmania (Viannia) disease pathogenesis is unclear. Using the mouse model of chronic L. (V.) panamensis infection, we examined the hypothesis that Treg functionality contributes to control of pathogenesis. Upon infection, Tregs (CD4(+)Foxp3(+)) presented with a dysregulated phenotype, in that they produced IFN-γ, expressed Tbet, and had a reduced ability to suppress T cell proliferation in vitro. Targeted ablation of Tregs resulted in enlarged lesions, increased parasite load, and enhanced production of IL-17 and IFN-γ, with no change in IL-10 and IL-13 levels. This indicated that an increased inflammatory response was commensurate with disease exacerbation and that the remaining impaired Tregs were important in regulation of disease pathology. Conversely, adoptive transfer of Tregs from naive mice halted disease progression, lowered parasite burden, and reduced cytokine production (IL-10, IL-13, IL-17, IFN-γ). Because Tregs appeared to be important for controlling infection, we hypothesized that their expansion could be used as an immunotherapeutic treatment approach. As a proof of principle, chronically infected mice were treated with rIL-2/anti-IL-2 Ab complex to expand Tregs. Treatment transitorily increased the numbers and percentage of Tregs (draining lymph node, spleen), which resulted in reduced cytokine responses, ameliorated lesions, and reduced parasite load (10(5)-fold). Thus, immunotherapy targeting Tregs could provide an alternate treatment strategy for leishmaniasis caused by Leishmania (Viannia) parasites.


Subject(s)
Immunotherapy, Adoptive , Leishmania guyanensis/immunology , Leishmaniasis, Mucocutaneous/immunology , Leishmaniasis, Mucocutaneous/therapy , T-Lymphocytes, Regulatory/immunology , Animals , Antibodies/immunology , Antibodies/therapeutic use , Antigen-Antibody Complex/therapeutic use , Cell Proliferation , Female , Indoleamine-Pyrrole 2,3,-Dioxygenase/antagonists & inhibitors , Inflammation/immunology , Interferon-gamma/biosynthesis , Interleukin-10/biosynthesis , Interleukin-13/biosynthesis , Interleukin-17/biosynthesis , Interleukin-2/immunology , Interleukin-2/therapeutic use , Leishmaniasis, Mucocutaneous/parasitology , Lymphocyte Count , Mice , Mice, Inbred BALB C , Mice, Transgenic , Parasite Load , T-Lymphocytes, Regulatory/transplantation , Transforming Growth Factor beta/biosynthesis
2.
Vet. parasitol ; 160(1/2): 18-24, 2009. tab
Article in English | Sec. Munic. Saúde SP, COVISA-Acervo | ID: sms-1338

ABSTRACT

To identify natural infections by Leishmania spp. in insect vectors of cutaneous and visceral leishmaniasis, we performed field studies in natural and anthropic environments in the Guaicurus Settlement (Bodoquena Range) of the Bonito municipality, Mato Grosso do Sul state, Brazil. From October 2002 to October 2003, a total of 1395 sandfly females were captured with Shannon and light traps and dissected in search of flagellates. The sample is composed of a total of 13 species, with Lutzomyia almerioi (59.9%) and Lutzomyia longipalpis (31.4%) predominant. Infections by flagellates were directly observed in three of the dissected of Lu. almerioi females (0.36%). To increase the sensitivity of detection, DNA extracted from pools of the 1220 dissected females (Lu. almerioi 808, Lu. longipalpis 399 and Nyssomyia whitmani 13) was subjected to small subunit rRNA-based polymerase chain reactions (SSU-PCR). DNA from Leishmania (L.) infantum chagasi was detected in at least 0.37% of Lu. almerioi females and in 0.25% of Lu. longipalpis females. The DNA of the Leishmania (Viannia) sp. was detected in 0.12% of Lu. almerioi and in 0.70% of Lu. longipalpis. Leishmania (L.) amazonensis was found in 1.25% of Lu. longipalpis. Mixed infections of L. (Leishmania) sp. and L. (Viannia) sp. were found in 0.50% of Lu. longipalpis. When considering that each positive pool contained at least a single infected specimen, we found a 1.23% rate of Leishmania spp. infection among the total population of dissected female sand flies as determined by PCR. This is the first report of natural infection by L. (L.) infantum chagasi and L. (Viannia) sp. in Lu. almerioi. It is also the first report of infection by L. (Viannia) sp. in Lu. longipalpis. The observation that Lu. longipalpis and Lu. almerioi are naturally infected by agents of both cutaneous and visceral leishmaniases suggests that these two species play a role in the transmission of these diseases within the study area. Furthermore, the finding that Lu. longipalpis has been naturally infected by L. (L.) amazonensis and L. (Viannia) sp., and Lu. almerioi by L. (L.) infantum chagasi and L. (Viannia), suggests their participation as permissive vectors


Subject(s)
Animals , Leishmania , Leishmaniasis, Visceral , Leishmaniasis, Cutaneous , Infections , Insect Vectors
3.
Vet Parasitol ; 160(1-2): 18-24, 2009 Mar 09.
Article in English | MEDLINE | ID: mdl-19062193

ABSTRACT

To identify natural infections by Leishmania spp. in insect vectors of cutaneous and visceral leishmaniasis, we performed field studies in natural and anthropic environments in the Guaicurus Settlement (Bodoquena Range) of the Bonito municipality, Mato Grosso do Sul state, Brazil. From October 2002 to October 2003, a total of 1395 sandfly females were captured with Shannon and light traps and dissected in search of flagellates. The sample is composed of a total of 13 species, with Lutzomyia almerioi (59.9%) and Lutzomyia longipalpis (31.4%) predominant. Infections by flagellates were directly observed in three of the dissected of Lu. almerioi females (0.36%). To increase the sensitivity of detection, DNA extracted from pools of the 1220 dissected females (Lu. almerioi 808, Lu. longipalpis 399 and Nyssomyia whitmani 13) was subjected to small subunit rRNA-based polymerase chain reactions (SSU-PCR). DNA from Leishmania (L.) infantum chagasi was detected in at least 0.37% of Lu. almerioi females and in 0.25% of Lu. longipalpis females. The DNA of the Leishmania (Viannia) sp. was detected in 0.12% of Lu. almerioi and in 0.70% of Lu. longipalpis. Leishmania (L.) amazonensis was found in 1.25% of Lu. longipalpis. Mixed infections of L. (Leishmania) sp. and L. (Viannia) sp. were found in 0.50% of Lu. longipalpis. When considering that each positive pool contained at least a single infected specimen, we found a 1.23% rate of Leishmania spp. infection among the total population of dissected female sand flies as determined by PCR. This is the first report of natural infection by L. (L.) infantum chagasi and L. (Viannia) sp. in Lu. almerioi. It is also the first report of infection by L. (Viannia) sp. in Lu. longipalpis. The observation that Lu. longipalpis and Lu. almerioi are naturally infected by agents of both cutaneous and visceral leishmaniases suggests that these two species play a role in the transmission of these diseases within the study area. Furthermore, the finding that Lu. longipalpis has been naturally infected by L. (L.) amazonensis and L. (Viannia) sp., and Lu. almerioi by L. (L.) infantum chagasi and L. (Viannia), suggests their participation as permissive vectors.


Subject(s)
Dog Diseases/parasitology , Leishmania/isolation & purification , Leishmaniasis, Cutaneous/parasitology , Leishmaniasis, Visceral/veterinary , Psychodidae/parasitology , Animals , Brazil/epidemiology , Dog Diseases/epidemiology , Dogs , Female , Humans , Insect Vectors/parasitology , Leishmaniasis, Cutaneous/epidemiology , Leishmaniasis, Visceral/epidemiology , Leishmaniasis, Visceral/parasitology
4.
Am J Trop Med Hyg ; 78(1): 122-32, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18187795

ABSTRACT

A real-time polymerase chain reaction (PCR) test was developed on the basis of the Leishmania glucose-6-phosphate dehydrogenase locus that enables identification and quantification of parasites. Using two independent pairs of primers in SYBR-Green assays, the test identified etiologic agents of cutaneous leishmaniasis belonging to both subgenera, Leishmania (Viannia) and Leishmania (Leishmania) in the Americas. Furthermore, use of TaqMan probes enables distinction between L. (V.) braziliensis or L. (V.) peruviania from the other L. (Viannia) species. All assays were negative with DNA of related trypanosomatids, humans, and mice. The parasite burden was estimated by normalizing the number of organisms per total amount of DNA in the sample or per host glyceraldehyde-3-phosphate dehydrogenase copies. The real-time PCR assay for L. (Leishmania) subgenus showed a good linear correlation with quantification on the basis of a limiting dilution assay in experimentally infected mice. The test successfully identifies and quantifies Leishmania in human biopsy specimens and represents a new tool to study leishmaniasis.


Subject(s)
Glucosephosphate Dehydrogenase/genetics , Leishmania/isolation & purification , Leishmaniasis, Cutaneous/diagnosis , Animals , Base Sequence , DNA Primers , DNA, Protozoan/analysis , Glucosephosphate Dehydrogenase/metabolism , Humans , Leishmania/classification , Leishmania/enzymology , Leishmania/genetics , Leishmaniasis, Cutaneous/parasitology , Mice , Mice, Inbred BALB C , Molecular Sequence Data , Predictive Value of Tests , Reverse Transcriptase Polymerase Chain Reaction , Sensitivity and Specificity , Sequence Alignment
5.
Mem. Inst. Oswaldo Cruz ; 100(7): 739-741, Nov. 2005. ilus
Article in English | LILACS | ID: lil-419699

ABSTRACT

A natural case of co-infection by Leishmania and Trypanosoma is reported in a dog (Canis familiaris) in south- western state of Mato Grosso do Sul, Brazil. Both amastigote and trypomastigote forms were observed after Giemsa staining of cytological preparations of the dog's bone marrow aspirate. No parasite was detected using medium culture inoculation of the sample. DNA obtained from the bone marrow aspirate sample and from the blood buffy coat was submitted to polymerase chain reaction (PCR) with a set of rDNA-based primers S4/S12. The nucleotide sequence of the PCR product was identical to that of Trypanosoma (Trypanozoon) evansi. The S4/S12 PCR was then used as template in a nested-PCR using a specific Leishmania set S17/S18 as primers, to explain the amastigote forms. The nucleotide sequence of the new PCR product was identical to that of Leishmania (Leishmania) chagasi. This case, as far as we know, is the first report of a dog co-infected with these parasites, suggesting that besides L. (L.) chagasi, the natural transmission of T. (T.) evansi occurs in the area under study.


Subject(s)
Dogs , Animals , Dog Diseases/diagnosis , Leishmaniasis, Visceral/veterinary , Trypanosomiasis/veterinary , Brazil , DNA, Ribosomal/analysis , DNA, Viral/classification , Dog Diseases/parasitology , Leishmania infantum/genetics , Leishmania infantum/immunology , Leishmaniasis, Visceral/complications , Leishmaniasis, Visceral/diagnosis , Trypanosoma/genetics , Trypanosoma/immunology , Trypanosomiasis/complications , Trypanosomiasis/diagnosis
6.
Mem Inst Oswaldo Cruz ; 100(7): 739-41, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16410962

ABSTRACT

A natural case of co-infection by Leishmania and Trypanosoma is reported in a dog (Canis familiaris) in south- western state of Mato Grosso do Sul, Brazil. Both amastigote and trypomastigote forms were observed after Giemsa staining of cytological preparations of the dog's bone marrow aspirate. No parasite was detected using medium culture inoculation of the sample. DNA obtained from the bone marrow aspirate sample and from the blood buffy coat was submitted to polymerase chain reaction (PCR) with a set of rDNA-based primers S4/S12. The nucleotide sequence of the PCR product was identical to that of Trypanosoma (Trypanozoon) evansi. The S4/S12 PCR was then used as template in a nested-PCR using a specific Leishmania set S17/S18 as primers, to explain the amastigote forms. The nucleotide sequence of the new PCR product was identical to that of Leishmania (Leishmania) chagasi. This case, as far as we know, is the first report of a dog co-infected with these parasites, suggesting that besides L. (L.) chagasi, the natural transmission of T. (T.) evansi occurs in the area under study.


Subject(s)
Dog Diseases/diagnosis , Leishmaniasis, Visceral/veterinary , Trypanosomiasis/veterinary , Animals , Brazil , DNA, Protozoan/analysis , DNA, Ribosomal/analysis , Dog Diseases/parasitology , Dogs , Leishmania infantum/genetics , Leishmania infantum/immunology , Leishmaniasis, Visceral/complications , Leishmaniasis, Visceral/diagnosis , Trypanosoma/genetics , Trypanosoma/immunology , Trypanosomiasis/complications , Trypanosomiasis/diagnosis
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