Literature DB >> 7913112

Adult and microfilarial stages of the filarial parasite Brugia malayi stimulate contrasting cytokine and Ig isotype responses in BALB/c mice.

R A Lawrence1, J E Allen, J Osborne, R M Maizels.   

Abstract

Natural infection with filarial nematode parasites shows many characteristics of a Th2 immune response. In these infections, long-lived adult worms inhabit the lymphatics, releasing laval microfilariae (Mf) into the blood stream. To compare the effect of these different developmental stages on the mammalian immune system, Mf and adult worms of either sex were implanted into BALB/c mice, in which they survive for at least 28 days. Serum Ab responses showed that whereas Mf stimulated specific Abs of all IgG subclasses, but little total IgE, adult worms stimulated only IgG1 and IgE responses. Splenocytes from implanted mice were stimulated in vitro with specific Ag or Con A and assayed for proliferation and profiles of cytokine secretion. Cells from Mf-infected mice secreted high levels of IFN-gamma (30 U/ml) throughout infection, but very little IL-4 at the early time points. By day 28 postinfection, however, splenocytes from Mf-infected mice showed some IL-4 secretion in response to specific Ag (40 U/ml). The IFN-gamma response to Mf was found to be independent of the inoculum dose in the range of 10(2) to 10(6) organisms. In contrast, splenocytes taken from adult worm-implanted mice on days 14, 21, and 28 postinfection produced high levels of IL-4 (up to 435 U/ml) and negligible amounts of IFN-gamma despite the production of large numbers of Mf by adult female worms. CD4+ cells were primarily responsible for this IL-4 production. These results demonstrate that adult filarial parasites, and females in particular, exert a rapid polarization of the immune response in a Th2-like direction, but that this effect may be modulated by the Mf stage.

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Year:  1994        PMID: 7913112

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  30 in total

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3.  Infection of BALB/c mice with the filarial nematode Litomosoides sigmodontis: role of CD4+ T cells in controlling larval development.

Authors:  K M Al-Qaoud; A Taubert; H Zahner; B Fleischer; A Hoerauf
Journal:  Infect Immun       Date:  1997-06       Impact factor: 3.441

4.  Signaling through Galphai2 protein is required for recruitment of neutrophils for antibody-mediated elimination of larval Strongyloides stercoralis in mice.

Authors:  Udaikumar M Padigel; Louis Stein; Kevin Redding; James J Lee; Thomas J Nolan; Gerhard A Schad; Lutz Birnbaumer; David Abraham
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5.  Fine specificity of the genetically controlled immune response to native and recombinant gp15/400 (polyprotein allergen) of Brugia malayi.

Authors:  J E Allen; R A Lawrence; R M Maizels
Journal:  Infect Immun       Date:  1995-08       Impact factor: 3.441

6.  Interleukin-4 is essential for the control of microfilariae in murine infection with the filaria Litomosoides sigmodontis.

Authors:  L Volkmann; M Saeftel; O Bain; K Fischer; B Fleischer; A Hoerauf
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7.  Comparative analysis of glycosylated and nonglycosylated filarial homologues of the 20-kilodalton retinol binding protein from Onchocerca volvulus (Ov20).

Authors:  N Nirmalan; N J Cordeiro; S L Kläger; J E Bradley; J E Allen
Journal:  Infect Immun       Date:  1999-12       Impact factor: 3.441

8.  Nitric oxide limits the expansion of antigen-specific T cells in mice infected with the microfilariae of Brugia pahangi.

Authors:  Richard A O'Connor; Eileen Devaney
Journal:  Infect Immun       Date:  2002-11       Impact factor: 3.441

9.  Antibody isotype analysis of malaria-nematode co-infection: problems and solutions associated with cross-reactivity.

Authors:  Karen J Fairlie-Clarke; Tracey J Lamb; Jean Langhorne; Andrea L Graham; Judith E Allen
Journal:  BMC Immunol       Date:  2010-02-17       Impact factor: 3.615

10.  T cells are required for host protection against Brugia malayi but need not produce or respond to interleukin-4.

Authors:  L Spencer; L Shultz; T V Rajan
Journal:  Infect Immun       Date:  2003-06       Impact factor: 3.441

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