1997
DOI: 10.1007/bf02873052
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Immunomodulation of excretory secretory materials from the filarial parasiteSetaria digitata

Abstract: ES materials released along with the release of mf showed immunosuppression as evidenced by a decrease in T =ymphocyte levels in the immunised animals. Lipid fractions of the mf associated ES materials and protein fractions of the detergent soluble materials were fuund to cause suppression of immune response in the host. Further study revealed that the suppression associated with the lipid fractions is actually the end result and that mf associated ES materials is actually a mixture of immunosuppressive and im… Show more

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“…Although an antifilarial immune response is generated for the shed antigens, parasites evade this immune response by ‘surface epitope hiding’; grooves and striations on the adult parasite surface may be ideal for antigenic concealment (Bright & Raj, 1994). ES material demonstrated immunosuppression, evident by depleted T-cell levels, and this effect was attributed to lipids and not proteins of ES material (Raj et al , 1997). Generally, filarial infections mount a T-helper 2 (Th2)-type immune response in mammalian hosts, which constitutes increased production of interleukin (IL)-4, IL-10 and IL-13 cytokines, elevated IgG1, IgG4 and IgE antibody isotypes and other innate-immune cells (Babu & Nutman, 2012).…”
Section: Immunologymentioning
confidence: 99%
“…Although an antifilarial immune response is generated for the shed antigens, parasites evade this immune response by ‘surface epitope hiding’; grooves and striations on the adult parasite surface may be ideal for antigenic concealment (Bright & Raj, 1994). ES material demonstrated immunosuppression, evident by depleted T-cell levels, and this effect was attributed to lipids and not proteins of ES material (Raj et al , 1997). Generally, filarial infections mount a T-helper 2 (Th2)-type immune response in mammalian hosts, which constitutes increased production of interleukin (IL)-4, IL-10 and IL-13 cytokines, elevated IgG1, IgG4 and IgE antibody isotypes and other innate-immune cells (Babu & Nutman, 2012).…”
Section: Immunologymentioning
confidence: 99%