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SG27 is a salivary gland protein from the black-legged tick, Ixodes scapularis, which is the primary vector for Lyme disease in North America [17, 23]. It is one of the 19 key antigens included in the 19ISP mRNA-LNP vaccine, a novel therapeutic approach designed to induce acquired resistance to ticks (ATR) in the host [23, 59]. By targeting SG27 and other salivary proteins, the vaccine triggers an immune response that interferes with the tick's ability to feed and remain attached to the host [28, 63]. This immune recognition often manifests as rapid erythema at the bite site, which serves as a biological signal for the host to remove the tick before pathogen transmission occurs [23, 28]. SG27 plays a role in the complex interface between the tick and the host's skin, facilitating the blood meal and potentially suppressing local host defenses [23, 31]. The development of vaccines targeting SG27 represents a shift from targeting the pathogen itself to targeting the vector's ability to transmit the disease [17, 43].
Induction of acquired resistance to ticks (ATR) via host antibodies (IgG) that recognize SG27 in tick saliva, leading to early erythema, reduced feeding, and early detachment.
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