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Infection and Immunity, August 1994, p. 3270-3275, Vol. 62, No. 8
0019-9567/1994/$04.00+0     DOI:

research-article

Immunogenicity of the Plasmodium falciparum glutamate-rich protein expressed by vaccinia virus.

M Theisen, G Cox, B Høgh, S Jepsen, and J Vuust

Department of Infection-Immunology, Statens Seruminstitut, Copenhagen, Denmark.

ABSTRACT

The glurp gene of Plasmodium falciparum F32 has been inserted into a vaccinia virus, and the recombinant virus was designated VVG4. Expression of glurp in VVG4-infected Vero cells was analyzed by immunoprecipitation and revealed a primary GLURP product of approximately 220,000 Da; GLURP was detected both intracellularly and in culture supernatants. To study the immunogenicity of vaccinia virus-expressed GLURP, mice were immunized with VVG4 and serum samples were analyzed for antibody reactivity with three polypeptides, covering almost the entire GLURP molecule; these three polypeptides were produced in recombinant form in Escherichia coli. The immune response was primarily directed against a carboxy-terminal repeat region. The mouse anti-GLURP serum recognized authentic GLURP by immunoprecipitation analysis from P. falciparum grown in vitro. These results demonstrate that vaccinia virus-expressed glurp product can induce a humoral immune response against GLURP derived from blood-stage parasites.


Infection and Immunity, August 1994, p. 3270-3275, Vol. 62, No. 8
0019-9567/1994/$04.00+0     DOI:




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