Analysis of the protective potential of antigens released by Leishmania (Viannia) shawi promastigotes
Carregando...
Citações na Scopus
3
Tipo de produção
article
Data de publicação
2012
Título da Revista
ISSN da Revista
Título do Volume
Editora
SPRINGER
Autores
MARQUES, Claudia
VALE-GATO, Ines
SANTOS-GOMES, Gabriela
Citação
ARCHIVES OF DERMATOLOGICAL RESEARCH, v.304, n.1, p.47-55, 2012
Resumo
Leishmania (Viannia) shawi causes cutaneous lesions in humans. Parasite antigens conferring significant protection against American tegumentar leishmaniosis (ATL) might be important for the development of effective vaccine. Therefore, this work evaluates the protective effect of antigenic fractions released by L. shawi. Antigens released by promastigotes to culture medium were concentrated and isolated by SDS-PAGE. The three main fractions LsPass1 (>75 kDa), LsPass2 (75-50 kDa) and LsPass3 (<50 kDa) were electro-eluted according with their molecular mass. Immunized BALB/c mice were challenged with L. shawi promastigotes and the course of infection monitored during 5 weeks. LsPass1-challenged mice showed no protection, however, a strong degree of protection associated to smaller lesions and high expression of IFN-gamma and TNF-alpha by CD4(+) T, CD8(+) T and double negative CD4CD8 cells was achieved in LsPass3-challenged mice. Furthermore, LsPass2-challenged mice showed an intermediated degree of protection associated to high levels of IFN-gamma, IL-4 and IL-10 mRNA. In spite of increased expression of IFN-gamma and TNF-alpha, high amounts of IL-4 and IL-10 mRNA were also detected in LsPass3-challenged mice indicating a possible contribution of these cytokines for the persistence of a residual number of parasites that may be important in inducing long-lasting immunity. Therefore, LsPass3 seems to be an interesting alternative that should be considered in the development of an effective vaccine against ATL.
Palavras-chave
Leishmania shawi, Released antigens, Immunization
Referências
- Bogdan C, 2008, CELL MICROBIOL, V10, P1221, DOI 10.1111/j.1462-5822.2008.01146.x
- Brito MEF, 2009, TROP MED INT HEALTH, V14, P1278, DOI 10.1111/j.1365-3156.2009.02361.x
- Carneiro FP, 2009, PARASITE IMMUNOL, V31, P646, DOI 10.1111/j.1365-3024.2009.01148.x
- Chen GJ, 2009, AM J PATHOL, V175, P1086, DOI 10.2353/ajpath.2009.080488
- Darrah PA, 2010, J EXP MED, V207, P1421, DOI 10.1084/jem.20092532
- Dunning O, 2009, BIOSCI HORIZ, V2, P73
- Filippi CM, 2008, DIABETES, V57, P2684, DOI 10.2337/db08-0609
- Ivory C, 2004, GENET VACCINES THER, V2, P17, DOI 10.1186/1479-0556-2-17
- Kang JS, 2009, TRENDS CELL BIOL, V19, P385, DOI 10.1016/j.tcb.2009.05.008
- Kaufmann SHE, 1999, IMMUNOL LETT, V65, P81, DOI 10.1016/S0165-2478(98)00128-X
- KREUTZER RD, 1991, AM J TROP MED HYG, V44, P662
- LAEMMLI UK, 1970, NATURE, V227, P680, DOI 10.1038/227680a0
- LAINSON R, 1989, ANN PARASIT HUM COMP, V64, P200
- LAINSON R, 1989, ANN PARASIT HUM COMP, V64, P3
- Lemesre JL, 2007, VACCINE, V25, P4223, DOI 10.1016/j.vaccine.2007.02.083
- Lemesre JL, 2005, VACCINE, V23, P2825, DOI 10.1016/j.vaccine.2004.11.061
- LIEW FY, 1990, J IMMUNOL, V145, P4306
- Nagill R, 2009, PARASITOL INT, V58, P359, DOI 10.1016/j.parint.2009.07.008
- Naundorf S, 2009, EUR J IMMUNOL, V39, P1066, DOI 10.1002/eji.200838773
- Novoa R, 2011, PARASITE IMMUNOL, V33, P132, DOI 10.1111/j.1365-3024.2010.01256.x
- O'Daly JA, 2010, ARCH DERMATOL RES, V302, P95, DOI 10.1007/s00403-009-0992-0
- O'Daly JA, 2009, ARCH DERMATOL RES, V301, P411, DOI 10.1007/s00403-009-0940-z
- O'Daly JA, 2010, ARCH DERMATOL RES, V302, P567, DOI 10.1007/s00403-009-1026-7
- O'Daly JA, 2009, ARCH DERMATOL RES, V301, P1, DOI 10.1007/s00403-008-0883-9
- O'Daly JA, 2011, ARCH DERMATOL RES, V303, P399, DOI 10.1007/s00403-011-1133-0
- Okwor I, 2008, IMMUNOL RES, V41, P123, DOI 10.1007/s12026-008-8016-2
- Passero LFD, 2009, PARASITOL RES, V105, P1741, DOI 10.1007/s00436-009-1614-7
- Passero LFD, 2010, PARASITOL INT, V59, P159, DOI 10.1016/j.parint.2009.12.010
- Passero LFD, 2010, APMIS, V118, P973, DOI 10.1111/j.1600-0463.2010.02679.x
- Rodrigues OR, 2009, IMMUNOBIOLOGY, V214, P101, DOI 10.1016/j.imbio.2008.07.001
- Rodrigues OR, 2006, CELL IMMUNOL, V243, P118, DOI 10.1016/j.cellimm.2007.01.005
- Rodriguez-Cortees A, 2007, VACCINE, V25, P7962, DOI 10.1016/j.vaccine.2007.08.023
- Rosa R, 2005, EXP PARASITOL, V109, P106, DOI 10.1016/j.exppara.2004.11.008
- Rosa R, 2007, VACCINE, V25, P4525, DOI 10.1016/j.vaccine.2007.03.003
- Santarem N, 2007, J BIOMED BIOTECHNOL, DOI 10.1155/2007/85154
- Shanmugasundaram R, 2010, VET IMMUNOL IMMUNOP, V137, P161, DOI 10.1016/j.vetimm.2010.04.017
- SHAW JJ, 1991, ANN PARASIT HUM COMP, V66, P243
- Silveira FT, 2004, MEM I OSWALDO CRUZ, V99, P239, DOI 10.1590/S0074-02762004000300001
- Silveira FT, 2002, PARASITE, V9, P43
- Souza-Lemos C, 2008, J PATHOL, V216, P375, DOI 10.1002/path.2403
- Taylor AW, 2009, J LEUKOCYTE BIOL, V85, P29, DOI 10.1189/jlb.0708415
- Tonui WK, 2004, INFECT IMMUN, V72, P5654, DOI 10.1128/IAI.72.10.5654-5661.2004
- Wolff J, 1990, SCIENCE, V1247, P1465