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Brugia malayi antigens represent a diverse collection of proteins and glycoconjugates expressed by the filarial nematode Brugia malayi, which is a primary cause of lymphatic filariasis [1]. These antigens are essential for the parasite's life cycle, playing roles in larval molting, host tissue penetration, and the sophisticated modulation of the host's immune system to ensure parasite survival [2]. In clinical diagnostics, specific antigens such as BmR1 and Bm14 are used to detect host IgG4 antibodies, providing a reliable method for identifying active or past infections [3]. Although no human vaccine is currently available, several antigens like Bm-ALT-2 and Bm-HSP70 are under investigation as recombinant vaccine candidates designed to stimulate protective immunity [4]. Current therapeutic strategies utilize anthelmintic drugs like diethylcarbamazine and ivermectin to eliminate the parasites, thereby reducing the production and circulation of these antigens in the host [5]. However, the rapid destruction of the parasites can lead to the sudden release of high levels of antigens, potentially triggering severe systemic inflammatory reactions known as the Mazzotti reaction [5].
Anthelmintic drugs disrupt the parasite's neuromuscular transmission or microtubule assembly to reduce antigenic load, while experimental vaccines target these antigens to induce protective neutralizing antibodies and T-cell responses [2, 5].
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