| Literature DB >> 35467360 |
Rojelio Mejia1, Sasisekhar Bennuru1, Yelena Oksov2, Sara Lustigman2, Gnanasekar Munirathinam3, Ramaswamy Kalyanasundaram3, Thomas B Nutman1.
Abstract
A molecule we termed Brugia malayi IL-5 receptor (IL-5R) binding protein (BmIL5Rbp; also known as Bm8757) was identified from B. malayi filarial worms and found to inhibit human interleukin-5 (IL-5) binding to its human receptor competitively. After the expression and purification of a recombinant BmIL5Rbp and generation of BmIL5Rbp-specific rabbit antibody, we localized the molecule on B. malayi worms through immunohistochemistry and immunoelectron microscopy. RNA interference (RNAi) was used to inhibit BmIL5Rbp mRNA and protein production. BmIL5Rbp was shown to localize to the cuticle of Brugia malayi and to be released in its excretory/secretory products. RNAi inhibited BmIL5Rbp mRNA production by 33%, reduced the surface protein expression by ~50%, and suppressed the release of BmIL5Rbp in the excretory/secretory products. RNAi has been used successfully to knock down the mRNA and protein expression of BmIL5Rbp in the early larval stages of B. malayi and provided a proof of principle for the local inhibition of the human IL-5R. These findings provide evidence that a parasite-encoded IL-5R antagonist may locally inhibit a vital host innate immune activation of IL-5 on eosinophils.Entities:
Keywords: Brugia malayi; RNAi; host-parasite defense; interleukin-5
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Year: 2022 PMID: 35467360 PMCID: PMC9119061 DOI: 10.1128/iai.00317-21
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.609