Literature DB >> 9698870

Reinfection in American cutaneous leishmaniasis: evaluation of clinical outcomes in the hamster model.

Y Osorio1, S J Gonzalez, V L Gama, B L Travi.   

Abstract

There is no clear understanding of the outcome of reinfection in New World cutaneous leishmaniasis, and its role in the relationship to the development of protection or secondary disease. For this reason, reinfection experiments with homologous (Leishmania panamensis-L. panamensis) and heterologous (L. major-L. panamensis) species of leishmaniae were conducted in the hamster model. The different protocols for primary infections prior to the challenge with L. panamensis were as follows: (a) L. major, single promastigote injection, (b) L. major, three booster infections, (c) L. panamensis, followed by antimonial treatment to achieve subclinical infection, (d) L. panamensis, with active lesions, (by antimonial treatment to achieve subclinical infection, (d) L. panamensis, with active lesions, (e) sham infected, naive controls. Although all reinfected hamsters developed lesions upon challenge, animals with active primary lesions due to L. panamensis, and receiving booster infections of L. major had the most benign secondary lesions (58-91% and 69-76% smaller than controls, respectively, P < 0.05). Subclinically infected animals had intermediate lesions (40-64% smaller than controls, P < 0.05), while hamsters which received a single dose of L. major had no significant improvement over controls. Our results suggested that L. major could elicit a cross protective response to L. panamensis, and that the presence and number of amastigotes persisting after a primary infection may influence the clinical outcome of reinfections.

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Year:  1998        PMID: 9698870     DOI: 10.1590/s0074-02761998000300015

Source DB:  PubMed          Journal:  Mem Inst Oswaldo Cruz        ISSN: 0074-0276            Impact factor:   2.743


  4 in total

1.  Simultaneous infection with Leishmania (Viannia) braziliensis and L. (V.) lainsoni in a Peruvian patient with cutaneous leishmaniasis.

Authors:  Nicolas Veland; Braulio Mark Valencia; Milena Alba; Vanessa Adaui; Alejandro Llanos-Cuentas; Jorge Arevalo; Andrea K Boggild
Journal:  Am J Trop Med Hyg       Date:  2013-02-04       Impact factor: 2.345

2.  Development of an Amplicon-Based Next-Generation Sequencing Protocol to Identify Leishmania Species and Other Trypanosomatids in Leishmaniasis Endemic Areas.

Authors:  Luz H Patiño; Adriana C Castillo-Castañeda; Marina Muñoz; Jesus E Jaimes; Nicolas Luna-Niño; Carolina Hernández; Martha S Ayala; Patricia Fuya; Claudia Mendez; Carlos E Hernández-Pereira; Lourdes Delgado; Claudia M Sandoval-Ramírez; Plutarco Urbano; Alberto Paniz-Mondolfi; Juan David Ramírez
Journal:  Microbiol Spectr       Date:  2021-10-13

3.  The compositional landscape of minicircle sequences isolated from active lesions and scars of American cutaneous leishmaniasis.

Authors:  Eduardo Henrique Gomes Rodrigues; Fábia Carla da Silva Soares; Roberto Pereira Werkhäuser; Maria Edileuza F de Brito; Octavio Fernandes; Frederico G Coutinho Abath; Adeilton Brandão
Journal:  Parasit Vectors       Date:  2013-08-07       Impact factor: 3.876

4.  Body weight as a determinant of clinical evolution in hamsters (Mesocricetus auratus) infected with Leishmania (Viannia) panamensis.

Authors:  Angela María Gómez-Galindo; Lucy Gabriela Delgado-Murcia
Journal:  Rev Inst Med Trop Sao Paulo       Date:  2013 Sep-Oct       Impact factor: 1.846

  4 in total

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