Nj. Singh et al., Characterization of a differential immunoscreen epitope of Plasmodium falciparum using combinatorial agents, PARASITE IM, 22(7), 2000, pp. 333-340
A differential serological screening of a lambda gt11 cDNA expression libra
ry has identified several clones, which react exclusively to sera samples f
rom persons clinically immune to malaria but not to acute malaria patient s
era. One such clone, IPf9, has a 315-bp cDNA insert, which was found to be
conserved in different strains of the human and rodent malarial parasite Pl
asmodium falciparum and Plasmodium berghei, respectively. The induced expre
ssion product of IPf9 was used to generate polyclonal sera in rabbits. The
IPf9 expression product was also screened with phage surface display combin
atorial libraries to isolate reagents that specifically bound to the IPf9 p
roduct. The polyclonal antisera and the combinatorial reagents recognized a
50-kDa protein from P. falciparum, and a 53-kDa product from P. berghei. I
mmunofluorescence studies using asexual and sexual stages of P. falciparum
showed the protein to be present within the parasite in each of the asexual
and sexual stages. The combinatorial reagents showed a partial inhibition
in the growth of P. falciparum in vitro. Mice infected with the P. berghei
showed the presence of T-cells that exhibited lymphoproliferation when stim
ulated with the IPf9 protein. It is suggested that IPf9 protein is a conser
ved protein epitope, and may be relevant for a protective immune response t
o malaria.