Passive Immunization with Antibodies against Three Distinct Epitopes onPlasmodium yoeliiMerozoite Surface Protein 1 Suppresses Parasitemia

Infection and Immunity - Tập 66 Số 8 - Trang 3925-3930 - 1998
Lilian Spencer1, Solabomi A. Ogun1, Suzanne L. Fleck1, Irene T. Ling1, Terry J. Scott-Finnigan1, Michael J. Blackman1, Anthony A. Holder1
1Division of Parasitology, National Institute for Medical Research, London NW7 1AA, United Kingdom

Tóm tắt

ABSTRACTWe have produced monoclonal antibodies againstPlasmodium yoeliimerozoite surface protein 1 (MSP-1) and have assessed their ability to suppress blood stage parasitemia by passive immunization. Six immunoglobulin G antibodies were characterized in detail: three (B6, D3, and F5) were effective in suppressing a lethal blood stage challenge infection, two (B10 and G3) were partially effective, and one (B4) was ineffective. MSP-1 is the precursor to a complex of polypeptides on the merozoite surface; all of the antibodies bound to this precursor and to an ∼42-kDa fragment (MSP-142) that is derived from the C terminus of MSP-1. MSP-142is further cleaved to an N-terminal ∼33-kDa polypeptide (MSP-133) and a C-terminal ∼19-kDa polypeptide (MSP-119) comprised of two epidermal growth factor (EGF)-like modules. D3 reacted with MSP-142but not with either of the constituents MSP-133and MSP-119, B4 recognized an epitope within the N terminus of MSP-133, and B6, B10, F5, and G3 bound to MSP-119. B10 and G3 bound to epitopes that required both C-terminal EGF-like modules for their formation, whereas B6 and F5 bound to epitopes in the first EGF-like module. These results indicate that at least three distinct epitopes onP. yoeliiMSP-1 are recognized by antibodies that suppress parasitemia in vivo.

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